ABSTRACT Aberrant activation of Wnt/β-catenin signaling has been associated with the onset and progression of many types of tumors and thus β-catenin represents one attractive intracellular

target for cancer therapy. Based on the Axin-derived peptide that binds to β-catenin, two stapled peptides SAHPA1 and xStAx were reported to enhance or impair Wnt/β-catenin signaling,

respectively. In this study, we designed PROTACs (proteolysis targeting chimeras) by coupling SAHPA1 or xStAx with the VHL ligand to achieve efficient β-catenin degradation. The obtained

xStAx-VHLL sustained β-catenin degradation and manifested strong inhibition of Wnt signaling in cancer cells and in _APC__−/−_ organoids. Furthermore, xStAx-VHLL could effectively restrain

of promising anticancer agent. SIMILAR CONTENT BEING VIEWED BY OTHERS A MICROPROTEIN N1DARP ENCODED BY LINC00261 PROMOTES NOTCH1 INTRACELLULAR DOMAIN (N1ICD) DEGRADATION VIA DISRUPTING

USP10-N1ICD INTERACTION TO INHIBIT CHEMORESISTANCE IN NOTCH1-HYPERACTIVATED PANCREATIC CANCER Article Open access 15 September 2023 USP10 DRIVES CANCER STEMNESS AND ENABLES SUPER-COMPETITOR

SIGNALLING IN COLORECTAL CANCER Article Open access 23 October 2024 NAG-1/GDF15 AS A TUMOR SUPPRESSOR IN COLORECTAL CANCER: INHIBITION OF Β-CATENIN AND NF-ΚB PATHWAYS VIA INTERACTION WITH

EPCAM Article Open access 02 May 2025 INTRODUCTION The Wnt/β-catenin signaling pathway plays a pivotal role in cell proliferation, differentiation, and survival1,2. The components of

canonical Wnt signaling consist of extracellular Wnt ligands, transmembrane receptors Frizzled/LRP5/6 (low-density lipoprotein receptor-related protein), the intracellular destruction

complex (including APC, Axin, CK1, GSK3β, and β-TrCP) and β-catenin3. As the canonical Wnt signal transducer, the stability of β-catenin is tightly controlled by the interplay between Wnt

ligands, receptors and the destruction complex2. Once mutations occur to Wnt signaling components, excessive β-catenin accumulates in the cytoplasm and translocates into the nucleus to

promote cell proliferation4. Aberrant activation of Wnt signaling is highly implicated in various types of cancer, including colorectal cancer, in human, for example, hotspot mutations of

APC, Axin, and β-catenin have been found to drive tumorigenesis2. Hence, inhibition of the Wnt/β-catenin pathway has already become an important approach for cancer therapy, and β-catenin is

the most attractive intracellular target5. Many small-molecule inhibitors of Wnt/β-catenin signaling have been identified6. However, none of them has been approved for the clinical use. As

β-catenin is the central player of the canonical Wnt signaling and is frequently mutated in cancers, it is the most attractive target for cancer therapy. For instance, PRI-724, which can

disrupt the interaction between β-catenin and its co-activators, has been tested for clinical use7. One of the caveats of this type of inhibitors could be insufficient to disturb all the

protein–protein interactions due to the large binding interface and complicated binding partners in heterogeneous tumor tissue. Therefore, it is ideal to design inhibitors that can induce

β-catenin degradation4,8. The small-molecule MSAB is a such example9, although its specific binding site and the working mechanism are still unclear. Peptides are superior as therapeutics to

small molecules in interacting with β-catenin but still suffer from the poor membrane permeability and protease stability10. Peptide stapling chemistry developed by Verdine and coworkers,

takes advantage of ruthenium-catalyzed metathesis to crosslink the side chains of paired anchoring residues at suitable positions, and has been successfully applied to design various peptide

inhibitors with improved proteolytic stability, membrane permeability, and thus biological activity11,12. Modeled after the same Axin-derived peptide motif, we and Verdine lab independently

designed and prepared two different stapled helical peptides, termed as SAHPA1 and xStAx, respectively13,14. Both SAHPA1 and xStAx are capable of penetrating the cell membrane and binding

with β-catenin. Interestingly, SAHPA1 was shown to activate Wnt/β-catenin signaling, while xStAx inhibited it13,14. The opposite effect of these peptides could be due to their different

working mechanisms: xStAx blocks the β-catenin-TCF interaction in the nucleus, while SAHPA1 enhances the dissociation of β-catenin from Axin in the presence of Wnt. Nevertheless, it still

remains challenging to drive xStAx efficiently inhibit Wnt-dependent tumor growth in cell culture, and importantly, in vivo, due in part to the rapid accumulation of β-catenin in cancer. To

overcome these limitations of β-catenin inhibitors, new strategies are urgently in need to achieve the long-lasting degradation of β-catenin and thus tumor regression. In recent years,

proteolysis-targeting chimaeras (PROTACs) has emerged as a useful technology to efficiently degrade protein of interest in vivo15,16,17. PROTACs consist of two ligands connected by a linker,

with one ligand specifically binding to the protein of interest and the other ligand recruiting an E3 ligase. When PROTACs interact with the target protein and an E3 ligase concurrently,

the target protein will be poly-ubiquitinated and then undergo proteasomal degradation. Compared with traditional inhibitors that need a 1:1 (inhibitor:target) activity ratio, PROTACs can

continuously function and show sub-stoichiometric property18,19. For instance, a stabilized peptide-based PROTAC has been successfully developed to target estrogen receptor α for the

efficient degradation20. In this study, to achieve efficient elimination of β-catenin, we designed novel PROTAC β-catenin degraders by coupling SAHPA1 or xStAx with VHL (von Hippel-Lindau

protein) ligand via an Ahx chemical linker, termed as SAHPA1-VHLL and xStAx-VHLL, respectively. We found that xStAx-VHLL manifested strong inhibition of Wnt signaling and sustained

degradation of β-catenin in cancer cells and the intestinal organoids derived from wild-type and _APC_–/– mice. xStAx-VHLL also restrained tumor formation in xenograft mouse models and

reduced intestinal tumors in _APC__min/+_ mice. Besides, xStAx-VHLL potently inhibited the survival of the CRC patient-derived organoids. This study is the first attempt to block Wnt

signaling via PROTAC-mediated β-catenin degradation, highlighting the potential of PROTAC peptides as a new class of promising agents against the diseases caused by overactivation of

Wnt/β-catenin signaling. RESULTS DESIGN OF PROTAC Β-CATENIN DEGRADERS Based on the observation that the β-catenin binding domain of Axin (amino acid 469–482) forms a stable continuous

α-helix and fits into a shallow groove of β-catenin21, we and Verdine group designed stapled helical peptides that specifically targets β-catenin to modulate Wnt signaling13,14. Although two

of the stapled peptides (SAHPA1 and xStAx) shared high similarity in sequences, SAHPA1 acted as an agonist for Wnt signaling while xStAx functioned to inhibit the pathway. As both SAHPA1

and xStAx can specifically bind to β-catenin, we made use of these stapled peptides as the tethering site for the design of bifunctional PROTAC β-catenin degraders. The VHL recognition

peptide sequence, ALAPYIP that has already been widely used in the design of peptide-based PROTAC degraders16, is employed as a ligand for the VHL E3 ligase recruitment. SAHPA1 or xStAx is

conjugated to the VHL ligand via amide bonds with a simple 6-Aminocaproic acid as the linker, generating the two PROTAC peptides: SAHPA1-VHLL and xStAx-VHLL (Fig. 1a and Supplementary Fig.

S1a). After HPLC purification, the synthesized PROTACs were readily obtained with over 95% purities, as verified by ESI-MS (Supplementary Fig. S1b). As determined by isothermal titration

calorimetry (ITC) and pulldown assay, stapled peptides and the corresponding PROTACs displayed comparative binding potency with β-catenin (Supplementary Fig. S2). Furthermore, both xStAx and

xStAx-VHLL had similar membrane permeability and could efficiently enter into a cell (Supplementary Fig. S3a), but xStAx-VHLL was retained in the cell much longer (Supplementary Fig. S3b).

XSTAX-VHLL INDUCES DOSE-DEPENDENT AND DURABLE Β-CATENIN DEGRADATION Then we examined the activity of these PROTAC peptides to induce degradation of the endogenous β-catenin protein. After

treated with 70 μM peptides for 24 h, HEK293T cells were harvested for immunoblotting. As shown in Fig. 1b, SAHPA1 slightly enhanced the β-catenin level while xStAx decreased it. These

results were in agreement with the previous reports13,14. Similarly, xStAx-VHLL also reduced the β-catenin level. However, xStAx-VHLL significantly downregulated β-catenin protein level,

which was obviously lower than xStAx, when the cells were treated with Wnt3a (Fig. 1b). Of note, these peptides had no effect on other Wnt signaling components as examined. Similar data were

obtained with colorectal cancer (CRC) cells, including HCT116, SW480, and LoVo cells (Supplementary Fig. S4). HCT116 cells harbor β-catenin mutation, while both LoVo and SW480 cells have

_APC_ mutation22. As expected, xStAx-VHLL-induced reduction of β-catenin was mediated by the ubiquitination-proteasome system as xStAx-VHLL promoted β-catenin ubiquitination and the

proteasome inhibitor MG132 blocked β-catenin degradation (Fig. 1c, d). The VHL ligase activity was required for xStAx-VHLL to mediate β-catenin degradation as the VHL ligase inhibitor VH-298

blocked it in HEK293T and LoVo cells (Supplementary Fig. S5a, b). We also found that StAx-VHL could induce β-catenin degradation in a dose-dependent manner in CRC cells (Fig. 1e,

Supplementary Fig. S5c, d). Both xStAx and xStAx-VHLL started to induce β-catenin degradation as soon as 12 h post treatment. However, only xStAx-VHLL maintained β-catenin at a low level up

to 36 h (Fig. 1f). The wash-out experiment indicated that β-catenin was remained low after 24 h of xStAx-VHLL removal while β-catenin level was restored after 24 h of xStAx removal (Fig.

1g). Therefore, these results suggested that xStAx-VHLL was capable of achieving strong and sustained β-catenin degradation. XSTAX-VHLL INHIBITS WNT/Β-CATENIN SIGNALING We then examined the

effect of xStAx-VHLL on Wnt/β-catenin signaling using the Topflash-luciferase reporter in HEK293T cells. Wnt3a induced the expression of the reporter, and SAHPA1 slightly enhanced the Wnt3a

effect while xStAx exhibited an inhibitory effect (Fig. 2a), as previously reported14. Importantly, xStAx-VHLL was more potent in decreasing the Wnt3a-induced expression of the reporter,

whereas SAHPA1-VHLL still exhibited moderate enhancement of Wnt signaling. Furthermore, xStAx-VHLL showed a dose-dependent effect on Wnt signaling (Fig. 2b). A number of small-molecule

inhibitors have been reported to target β-catenin, including PRI-724 that disrupts the β-catenin-CBP interaction7, PNU-74654 that disrupts the β-catenin/TCF interaction7 and MSAB that

promotes β-catenin degradation9. We compared the inhibitory effect of xStAx-VHLL with those inhibitors as well as XAV939 that inhibits tankyrases and thus stabilizes Axin23,24. As shown in

Fig. 2c, xStAx-VHLL (70 μM) exhibited a comparable inhibition on Wnt-induced Topflash-luciferase to other inhibitors at the working concentration (10 μM). Of note, higher concentration of

small-molecule inhibitors caused cytotoxicity. As MSAB promotes β-catenin degradation like xStAx-VHLL, we further compared its effect on β-catenin in several cell lines. Both 10 μM MSAB and

50 μM xStAx-VHLL decreased β-catenin protein to a comparable level after 24 h treatment in HEK293T, HCT116, and SW480 cells (Fig. 2d–f). Interestingly, in LoVo cells, only xStAx-VHLL was

able to reduce the β-catenin protein level, while MSAB had no effect (Fig. 2g). Consistently, the proliferation of LoVo cells was hampered by xStAx-VHLL but not by MSAB (Fig. 2h). In

addition, xStAx-VHLL induced the durable degradation of β-catenin in HEK293T cells as long as 24 h post washout, while β-catenin protein level was restored after 24 h of MSAB removal (Fig.

2i). Together, these results suggest that xStAx-VHLL is a potent β-catenin degrader. XSTAX-VHLL RESTRAINS CELL PROLIFERATION AND TUMOR FORMATION OF COLORECTAL CANCER CANCERS As xStAx-VHLL

impairs Wnt signaling by promoting β-catenin degradation, we examined its effect on cell proliferation. As illustrated in Fig. 3a, b, both xStAx-VHLL significantly attenuated the

proliferation of LoVo and HCT116 cells. Next, to examine the influence of the peptides on tumor formation, 3 × 106 LoVo cells were pretreated with each peptide at 50 μM for 24 h, followed by

subcutaneous injection into BALB/C nude mice. After 3 weeks when tumors were visible, the mice were sacrificed for comparison of subcutaneous tumors among different groups. Of note, the

tumors originated from xStAx-VHLL pretreating cells were significantly smaller in size and weight (Fig. 3c). Consistently, immunoblotting analysis of the tumor extracts showed that the

β-catenin protein level in the xStAx-VHLL group was apparently decreased compared with other groups, indicating that xStAx-VHLL achieved effective and durable degradation of β-catenin (Fig.

3d). Furthermore, the Wnt target genes _Axin2_, _Cyclin D1_ and _Myc_ were also decreased in the tumors derived from xStAx-VHLL-treated LoVo cells (Supplementary Fig. S6). These data suggest

that xStAx-VHLL impedes CRC cells proliferation and restrains tumor formation. XSTAX-VHLL INHIBITS TUMOR GROWTH IN APCMIN/+ MOUSE MODEL To further explore whether the PROTAC xStAx-VHLL

peptide can eliminate the existing tumors, we took use of _APC__min/+_ mice that harbored a point mutation in the _APC_ gene, resulting in _APC_ deletion and constitutive activation of Wnt

signaling25. Because _APC__min_/+ mice can develop intestinal tumors around 10 weeks-old26, the 11 weeks-old _APC__min_/+ mice were intraperitoneally injected with 30 mg/kg vehicle DMSO or

peptides at every other day for 14 days. Then the mice were sacrificed for analysis of intestinal tumors. Although tumor number was slightly decreased in the SAHPA1-VHLL and xStAx groups,

the xStAx-VHLL dramatically reduced tumor number compared with that of 11 weeks-old mice before treatment (day 0) or with vehicle DMSO treatment (Fig. 4a). In agreement with it, the active

of β-catenin protein levels were also decreased compared with the vehicle group (Fig. 4b). To further confirm the in vivo activity of xStAx-VHLL, we used _Axin2__LacZ_ Wnt reporter mice to

examine _Axin2_ expression. After intraperitoneal injection of the peptides for 7 doses/14 days, the mice were sacrificed and small intestines prepared for in situ β-galactosidase staining.

xStAx-VHLL significantly blocked _Axin2_ expression (Fig. 4c). Taken together, these data indicate that xStAx-VHLL is an effective reagent to decrease the existing tumors. XSTAX-VHLL IMPEDES

THE GROWTH OF WILD-TYPE AND APC−/− ORGANOIDS In the past few years, intestinal organoids have become an ideal _ex vivo_ culture system to screen the drugs that influence the signaling

pathways involved in organoids survival and growth and treat cancer26. As Wnt/β-catenin signaling is essential to maintain intestinal organoid growth26,27, we then tested whether xStAx-VHLL

could impede the growth of intestinal organoids by achieving effective β-catenin degradation. Firstly, we cultured the wild-type organoids with peptides at 10 μM for 4 days (Fig. 5a).

xStAx-VHLL treatment obviously impeded organoid survival and bud formation, and this inhibitory effect was observed after 1 day treatment (Fig. 5a–c). Consistently, xStAx-VHLL treatment

reduced the β-catenin protein level while increased the cleaved caspase 3 level (Fig. 5d). The Wnt signaling target genes _Lgr5_, _Axin2_, _Cyclin D1_, and _Myc_ were remarkably decreased as

soon as 3 h treatment of xStAx-VHLL (Fig. 5e). Next, we chose the GFP-marked Lgr5+ organoids to observe the intestinal stem cell population28. As shown in Supplementary Fig. S7, Lgr5+

intestinal stem cells were reduced after 36 h treatment of xStAx-VHLL, and the viable cell population also decreased, consistent with the above caspase 3 activation. We also tested the

effect of xStAx-VHLL on the _APC_−/− organoids. The treatment of xStAx-VHLL (50 μM) significantly impeded the growth of _APC_−/− organoids, and the inhibitory effect was observed at day 3

(Fig. 5f, g). As shown in Fig. 5h, immunoblotting analysis showed that β-catenin protein level in of the organoids was greatly decreased after 24 h treatment of xStAx-VHLL, whereas the

cleaved caspase 3 increased. xStAx-VHLL achieved a strong inhibition on _APC__−/−_ organoid survival, whereas MSAB had a minimal effect (Supplementary Fig. S8a). Consistently, xStAx-VHLL

also downregulated the expression of the Wnt target genes _Axin2_, _Cyclin D1_, and _Myc_ in _APC__−/−_ organoids (Supplementary Fig. S8b). These results together suggest that the PROTAC

peptide xStAx-VHLL exhibits strong inhibitory effects on Wnt/β-catenin signaling in wild-type and _APC_-/- organoids. XSTAX-VHLL RESTRAINS THE SURVIVAL OF CRC PATIENT-DERIVED ORGANOIDS In

the majority of CRC patients, Wnt/β-catenin signaling is aberrantly activated. Owing to the successful 3D culture of colorectal cancer tissue derived organoids, we were able to test the

clinical potential of β-catenin targeted degrader xStAx-VHLL _ex vivo_. We collected 12 CRC samples (numbered from C-01 to C-12). The exon sequencing indicated the mutations of Wnt/β-catenin

pathway components in all tumor tissue (Supplementary Fig. S9). As shown in Fig. 6a, 10 μM xStAx-VHLL could potently inhibited the survival of the 11/12 patient-derived organoids in 4 days,

including C-05 that harbored multiple mutations of _LRP6, APC, AXIN2, CTNNB1_ (β-catenin), _TCF7L2, KRAS, TP53, SMAD4, PI3KCA_, and others. For example, xStAx-VHLL manifested a strong

inhibition function on C-08 and C-05 compared with the DMSO control (Fig. 6b, c and Supplementary Fig. S10). Consistently, xStAx-VHLL reduced the β-catenin protein level after 2 days

treatment (Fig. 6d). However, C-11 organoids, which harbored the mutations of _LRP6, APC_, _TCF7L2, KRAS, TP53_, and others, were insensitive to xStAx-VHLL, even though the β-catenin protein

level was decreased (Fig. 6e–g). It is possible that other signaling, rather than Wnt/β-catenin signaling, plays a major role in driving the growth and survival of C-11 organoids.

DISCUSSION As Wnt/β-catenin signaling pathway is activated in various cancers, including colorectal cancer, targeting β-catenin has been regarded as an important approach to treat these

diseases4,5. In this study, we generated two PROTAC peptides by coupling VHL ligand to the stapled peptides that have been shown to interact with β-catenin13,14: SAHPA1-VHLL and xStAx-VHLL.

We demonstrated that xStAx-VHLL acted as a potent PROTAC β-catenin degrader, efficiently promoting the proteasomal degradation of endogenous β-catenin in cancer cells and intestinal

organoids. xStAx-VHLL also efficiently inhibited Wnt signaling as well as cell proliferation, intestinal organoid growth, and tumor formation. This inhibitory effect was observed not only in

the systems with intact Wnt/β-catenin signaling, but also in the systems with APC-defective and constitutively active β-catenin mutations. Further, in CRC patient-derived tumor organoids,

xStAx-VHLL effectively restrained the survival of tumor organoids, which highlighted its clinical potential. In the past few years, several small molecules have been identified to target

β-catenin. It has been shown that MSAB interacts with β-catenin and then induces the proteasomal degradation of β-catenin9, and NRX promotes the β-catenin degradation by enhancing the

interaction between β-catenin and the ubiquitin E3 ligase βTrCP29. PRI-724, PNU-74654, and BC2059 are capable of disrupting the interactions between β-catenin and its co-activators7.

However, the specificity of small molecules is a general concern. Mimicking the β-catenin binding region of Axin, we and Verdine lab have independently designed stapled helical

peptides13,14. Although xStAx designed by Grossmann and coworkers exhibited an impressive inhibition on Wnt/β-catenin signaling, it could be less efficient for in vivo use to treat tumors as

the newly synthesized β-catenin can rapidly accumulate30. The PROTAC technique could aid small molecule inhibitors or peptides to exert better biological activities in vivo as PROTAC can

link the ubiquitin-proteasome system to induce effective degradation of targeted proteins16. Indeed, xStAx-VHLL was more potent than xStAx to inhibit Wnt/β-catenin signaling and attenuate

cell proliferation and organoid growth. More importantly, xStAx-VHLL was able to impede in vivo tumor formation in nude mouse xenografts and suppress the existing tumors in _APC__min_/+

mouse models, while xStAx had minimal effect in vivo. Traditional drug discovery heavily relies on cell-based or animal models, few of the candidate drugs succeed in patient-based clinical

studies. The patient-derived tumor organoids, which recapitulate the complexity and heterogeneity of tumors, have been shown to be an ideal model for drug screening and precision medicine26.

In this study, we have found that a potent inhibition of 11/12 patient-derived tumor organoids by xStAx-VHLL not only reveals that xStAx-VHLL is a promising anti-CRC drug candidate, but

also confirms that the patient-derived tumor organoids exhibit their advances in testing the effectiveness of PROTAC peptides. Although both SAHPA1 and xStAx were derived the same

β-catenin-binding peptide, unlike xStAx-VHLL, SAHPA1-VHLL had minimal effect on β-catenin stability and thus no much effect on Wnt/β-catenin signaling. It could be due to the promoting

effect of SAHPA-113 and the lower membrane permeability of SAHPA1-VHLL compared to xStAx-VHLL. There is more space for the improvement of the working efficacy of xStAx-VHLL. The VHL peptide

ligand inserted in this study consists of natural amino acids, which could be degraded once the PROTAC peptide enters the cell. Non-natural residues substitution instead of original ones,

such as reported hydroxyproline to replace regular proline31,32, could be an effective approach to enhance the proteolytic resistance of PROTAC. It was previously reported that peptide

double-stapling at both N-terminals and C-terminals rather than single stapling conferred striking protease resistance upon the lengthy peptide33. Moreover, Replacement of the VHL ligand

with other E3 ligands is worthy to be tested. Improvement of β-catenin-binding peptide could also be another direction. Grossmann and coworkers reported the optimization of xStAx through

homo-Arg replacement and N-terminal polar modification, which yielded NLS-StAx-h with highly membrane permeability34. Whether NLS-StAx-h is a better β-catenin ligand to design PROTAC may be

of interest. Last, optimization of the chemical linker is needed. The simple Ahx linker is a little bit short and more polar PEG linker bearing varying length should be taken into

consideration35. Nonetheless, as the first-generation PROTAC β-catenin degrader, xStAx-VHLL has already showed great promise in inhibiting tumor growth in vivo, and it could be employed as

the leading PROTAC for further optimization in Wnt signaling-interfering cancer therapy. MATERIALS AND METHODS CHEMICAL SYNTHESIS AND CHARACTERIZATION OF PROTACS All reagents were purchased

from Adamas-beta®, J&K Scientific, GL Biotech, Energy Chemical or Sinopharm Chemical Reagent Co. Ltd. Rink Amide MBHA resin (0.30 mmol/g loading) was purchased from Tianjin Nankai

Hecheng Science & Technology Co. Ltd. As a typical example, 400 mg Rink Amide MBHA resin was swelled with DCM (5 mL) for 20 min. Then the resin was treated with 20% piperidine/DMF/0.1 

mol/L Oxyma pure twice (5 min × 2), followed by washing with DMF (five times), DCM (five times) and DMF (five times) at 35 °C. For coupling of the natural amino acid, Fmoc-AA-OH (1 mmol),

DIC (1 mmol), Oxyma pure (1 mmol) and NMP (6 mL) were mixed for 1 min and then added to the resin at 60 °C. After 15 min, the resin was washed with DMF (five times), DCM (five times), and

DMF (five times). The peptide couplings of S5 and R8 were carried out over a single 2 h coupling cycle using 2 eq. of the Fmoc protected amino acids at 60 °C. The deprotection, washing,

coupling and washing steps were repeated until all the amino acid residues were assembled reagent. The peptide-bound resin was treated with 20% piperidine/DMF/0.1 mol/L Oxyma pure to remove

the Fmoc group from the N-terminus. After the resin was washed, it was treated with 5 mL solution of acetic anhydride and pyridine (1:1) for 20 min. Then the resin was washed with DMF (five

times), DCM (five times), and DMF (five times). The ring-closing metathesis reaction was carried out in 1,2-dichloroethane (DCE) at room temperature using Grubbs’ first-generation catalyst.

The resin was washed with DCM (three times), and DCE (three times) and then treated with 10 mM solution of Grubbs’ first-generation catalyst in DCE. After the first round of the 2 h

metathesis, we repeated the same procedure for a second round of catalyst treatment with fresh catalyst solution. Then the peptide-resin was washed with DMF (five times) and DCM (five

times). Peptides were cleaved from their resin by treatment with cocktail trifluoroacetic acid (TFA) (TFA/Triisopropylsilane (TIPS)/H2O = 95/2.5/2.5, v/v/v) for 2 h at room temperature.

After completion of the cleavage reaction, TFA was evaporated by blowing with Argon. The crude peptides were obtained by precipitation with 40 mL of cold diethyl ether and centrifugation at

3500 r/min for 3 mins (three times). The supernatant diethyl ether was decanted from the centrifuge tube, the crude peptides were allowed to air dry and purified by RP-HPLC to give the final

products. After elongation of the peptide and metathesis reaction were conducted on the resin according to a general protocol. Then, the Fmoc group was removed and the resin was treated

with Fmoc-Ahx-OH (4 eq.), DIC (4 eq.), Oxyma pure (4 eq.) and NMP (6 mL) for 15 min at 60 °C. The Fmoc group was removed and the resin was treated with fluorescein isothiocyanate (FITC, 2

eq.) and DIPEA (2 eq.) in DMF (6 mL) at room temperature overnight. The biotinylated labeling was carried out as routine amino acid. Cleavage was conducted following a general protocol and

crude peptide was purified by RP- HPLC to give the final products. ANTIBODIES, REAGENTS, AND CELL LINES Antibodies used in this study were as following: β-catenin and caspase3 were purchased

from Santa Cruz; GAPDH, cleaved caspase3, Axin1, Dvl2, GSK3β; TCF4 from Cell Signaling Technology and E-cadherin from BD Biosciences. XAV939 and VH-298 was purchased from MCE, MSAB from

Sigma, PRI-724 and PNU-74654 from Selleck. Peptides used in this study, including SAHPA1, SAHPA1-VHLL, xStAx and xStAx-VHLL, were dissolved in DMSO for 10 mM stock solution. Colorectal

cancer cell lines SW480, HCT116, and LoVo were obtained from ATCC. SW480 cells were cultured in L15 medium supplemented with 10% FBS (Hyclone) in a 37 °C humidified incubator without CO2.

HCT116 cells were cultured in McCoy’s 5 A medium supplemented with 10% FBS (Hyclone) in a 37 °C humidified incubator containing 5% CO2. LoVo cells were cultured in DMEM medium supplemented

with 10% FBS (Hyclone) in a 37 °C humidified incubator containing 5% CO2. TOPFLASH LUCIFERASE REPORTER ASSAY Dual luciferase reporter assay system (Promega) was used. HEK293T cells, cultured

in 24-well plates, were transfected with 200 ng Topflash plasmid and 30 ng Renilla plasmid for 3-well cells. At 12 h post-transfection, cells were treated with certain concentrations of

peptides with or without Wnt3a conditioned medium (CM) for another 24 h. Then harvested the cells for luciferase activity measurement. IMMUNOPRECIPITATION AND IMMUNOBLOTTING For

immunoprecipitation, the cells were lysed in TNE lysis buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% Nonidet P-40, and protease inhibitor cocktail). For the β-catenin ubiquitination

detection experiment, the raw cell lysates were heated to 95 °C for 5 min and sonicated to completely denature the proteins. After 18,000×_g_ centrifugation for 10 min, the lysates were

immunoprecipitated with specific antibody and protein A-Sepharose beads and then washed the beads with TNE buffer for three times before immunoblotting. MOUSE INTESTINE ORGANOID CULTURE

Mouse intestinal crypts isolation and organoid culture were performed as previously described36. Briefly, mouse intestine was cut longitudinally and washed three times with cold PBS. Villi

were carefully scraped away and small pieces (5 mm) of intestine were incubated in 0.5 M EDTA in PBS for 40 min on ice. These pieces were then vigorously suspended in cold PBS and the

mixture was passed through 70 μm cell strainer (BD Biosciences). The crypt fraction was enriched through centrifugation (3 min at 300–400 g). Then the crypts were embedded in Matrigel (BD

Biosciences) and seeded on 48-well or 24-well plates. The intestinal organoid culture medium consists of Advanced DMEM/F12 supplemented with Penicillin/Streptomycin, GlutaMAX-I, N2, B27 and

N-acetylcysteine (Sigma-Aldrich) and combination of growth factors including EGF (50 ng/mL, Invitrogen), Noggin (100 ng/mL, R&D) and R-spondin1 (500 ng/mL). The organoids were treated

with proper dilution of peptides in the medium. CRC PATIENT TUMOR TISSUE COLLECTION AND ETHICS STATEMENT Intestine tumor tissues were surgically resected and sampled, from 12 patients who

had been diagnosed with intestine tumors at Peking University Third Hospital, Beijing, China, as referred before37. All samples were obtained with informed consent, and the study was

approved by the Peking University Third Hospital Medical Science Research Ethics Committee (M2018083). All relevant ethical regulations of Peking University Third Hospital Medical Science

Research Ethics Committee were followed. PATIENT-DERIVED TUMOR ORGANOID CULTURE CRC patient tumor tissues were washed with cold HBSS. After removing the muscle tissue, the epithelial tumor

tissues were cut into small pieces and vigorously suspended. Then the tissue suspension was centrifuged (3 min at 300–400 g) and tumor fraction was enriched at the bottom. Next, the tumor

fraction was embedded in Matrigel (BD Biosciences) and seeded on 24-well plates with the culture medium, which includes Advanced DMEM/F12 supplemented with Penicillin/Streptomycin,

GlutaMAX-I, N2, B27, N-acetylcysteine (Sigma-Aldrich), CHIR-99021 (5 μM, Selleck), A-83–01 (0.5 μM, Cayman), SB202190 (10 μM, Selleck), gastrin (1 nM, Tocris), Y27632 (10 μM, Enzo), PEG2

(2.5 μM, Selleck), nicotinamide (10 mM, Sigma-Aldrich), EGF (50 ng/mL, Invitrogen), Noggin (100 ng/mL, R&D) and R-spondin1 (500 ng/mL). QUANTITATIVE RT-PCR Total RNA was extracted with

TRIzol (Invitrogen) and cDNA was prepared using Revertra Ace (Toyobo). Real-time PCR reactions were performed in triplicates on a LightCycler 480 (Roche). Relative target genes expression

values were normalized to GAPDH expression. Data were analyzed according to the ΔCT method. The following primers were used: _Lgr5_, 5′-CGGGACCTTGAAGATTTCCT-3′ and

5′-GATTCGGATCAGCCAGCTAC-3′; _Aixn2_, 5′-GCTCCAGAAGATCACAAAGAGC-3′ and 5′-AGCTTTGAGCCTTCAGCATC-3′; _Ccnd1_, 5′-GCCATCCAAACTGAGGAAAA-3′ and 5′-GATCCTGGGAGTCATCGGTA-3′; _Myc_, 5′-

GCTGTTTGAAGGCTGGATTTC-3′ and 5′-GATGAAATAGGGCTGTACGGAG-3′; and _Gapdh_, 5′-AAGAAGGTGGTGAAGCAG-3′ and 5′-TCATACCAGGAAATGAGC-3′. CELL PROLIFERATION ASSAY Equal number of cells (8000–10,000

cells) were seeded in the 24-well plates and then subjected to different treatments. The cell numbers were counted every 24 h with the CCK-8 cell counting kit (Dojindo Molecular

Technologies) according to manufacturer’s instructions. TUMOR FORMATION IN NUDE MICE LoVo cells cultured were pretreated with DMSO pr peptides (50 μM) for 24 h. Then the cells were digested

with trypsin and centrifuge (3 min at 300–400 g). Cell pellets were washed with cold PBS three times and the cell number was counted. The BALB/C nude mice were subcutaneously injected with 3

 × 106 cells. Three weeks later, the nude mice were sacrificed and dissected for tumors. Tumor weight was quantified. IMMUNOFLUORESCENCE The small intestines were isolated from _APC__min/+_

mice and fixed in 4% paraformaldehyde at room temperature overnight. Paraffin sections (5 μm) were cut (RM2235, Leica). The sections were de-paraffinized in xylene and graded alcohols,

followed by antigen retrieval in 95 °C water bath for 25 min, followed by permeabilization with 0.1% Triton X-100 for 15 min at 4 °C and block for 1 h at room temperature in 5% BSA. After

incubation overnight at 4 °C with the primary antibody (rabbit anti-Ki67, Abcam, ab15580, 1:300; mouse anti-β catenin, Santa Cruz, sc7963, 1:1000), the fluorescein-labeled secondary antibody

(Life Technologies, 1:300) was added for 1 h at room temperature. The sections were scanned using Olympus FV3000 Laser Scanning Microscope. _AXIN2_ LACZ Β-GALACTOSIDASE STAINING The small

intestines were isolated from _Axin2_LacZ reporter mice, washed with PBS and fixed in 4 % paraformaldehyde for 1 h at room temperature, then cut into small pieces (1 cm). The tissue pieces

were stained with in situ β-galactosidase staining kit (Beyotime) according to the manufacturer’s instruction. The stained tissues were transferred to tissue cassettes and paraffin blocks

prepared using standard methods. The tissues were sliced into 5 μm thick sections with paraffin slicing machine (RM2235, Leica) and subjected to hematoxylin staining. STATISTICAL ANALYSIS

All experiments were carried out with at least three biological replicates. GraphPad Prism 6 software was employed for statistical analysis. For reporter assays, qRT-PCR, cell proliferation

assays, immunofluorescence marker intensity and organoid experiment, statistical analysis was performed with two-way ANOVA. For immunoblot band intensity, tumor weight of nude mice, tumor

number of _APC__min/+_ mice and relative _Axin2_ expression level, statistical analysis was performed with one-way ANOVA. Results were presented as mean ± SD. _P_ < 0.05 was considered

statistically significant: *_P_ < 0.05, **_P_ < 0.01, and ***_P_ < 0.001. REFERENCES * Clevers, H., Loh, K. M. & Nusse, R. Stem cell signaling. An integral program for tissue

renewal and regeneration: Wnt signaling and stem cell control. _Science_ 346, 1248012 (2014). Article  Google Scholar  * Clevers, H. & Nusse, R. Wnt/beta-catenin signaling and disease.

_Cell_ 149, 1192–1205 (2012). Article  CAS  Google Scholar  * MacDonald, B. T., Tamai, K. & He, X. Wnt/beta-catenin signaling: components, mechanisms, and diseases. _Dev. Cell_ 17, 9–26

(2009). Article  CAS  Google Scholar  * Nusse, R. & Clevers, H. Wnt/beta-catenin signaling, disease, and emerging therapeutic modalities. _Cell_ 169, 985–999 (2017). Article  CAS  Google

Scholar  * Cui, C., Zhou, X., Zhang, W., Qu, Y. & Ke, X. Is beta-catenin a druggable target for cancer therapy? _Trends Biochem. Sci._ 43, 623–634 (2018). Article  CAS  Google Scholar 

* Krishnamurthy, N. & Kurzrock, R. Targeting the Wnt/beta-catenin pathway in cancer: update on effectors and inhibitors. _Cancer Treat. Rev._ 62, 50–60 (2018). Article  CAS  Google

Scholar  * Zhang, X. & Hao, J. Development of anticancer agents targeting the Wnt/beta-catenin signaling. _Am. J. Cancer Res._ 5, 2344–2360 (2015). CAS  PubMed  PubMed Central  Google

Scholar  * Harb, J., Lin, P. J. & Hao, J. Recent development of Wnt signaling pathway inhibitors for cancer therapeutics. _Curr. Oncol. Rep._ 21, 12 (2019). Article  Google Scholar  *

Hwang, S. Y. et al. Direct targeting of beta-catenin by a small molecule stimulates proteasomal degradation and suppresses oncogenic Wnt/beta-catenin signaling. _Cell Rep._ 16, 28–36 (2016).

Article  CAS  Google Scholar  * Li, X. et al. Dithiocarbamate-inspired side chain stapling chemistry for peptide drug design. _Chem. Sci._ 10, 1522–1530 (2019). Article  CAS  Google Scholar

  * Schafmeister, C. E., Po, J. & Verdine, G. L. An all-hydrocarbon cross-linking system for enhancing the helicity and metabolic stability of peptides. _J. Am. Chem. Soc._ 122,

5891–5892 (2000). Article  CAS  Google Scholar  * Li, X., Zou, Y. & Hu, H. G. Different stapling-based peptide drug design: mimicking a-helix as inhibitors of protein–protein

interaction. _Chin. Chem. Lett._ 29, 1088–1092 (2018). Article  CAS  Google Scholar  * Cui, H. K. et al. Design of stapled alpha-helical peptides to specifically activate Wnt/beta-catenin

signaling. _Cell Res._ 23, 581–584 (2013). Article  CAS  Google Scholar  * Grossmann, T. N. et al. Inhibition of oncogenic Wnt signaling through direct targeting of beta-catenin. _Proc. Natl

Acad. Sci. USA_ 109, 17942–17947 (2012). Article  CAS  Google Scholar  * Sakamoto, K. M. et al. Protacs: chimeric molecules that target proteins to the Skp1-Cullin-F box complex for

ubiquitination and degradation. _Proc. Natl Acad. Sci. USA_ 98, 8554–8559 (2001). Article  CAS  Google Scholar  * Lai, A. C. & Crews, C. M. Induced protein degradation: an emerging drug

discovery paradigm. _Nat. Rev. Drug Discov._ 16, 101–114 (2017). Article  CAS  Google Scholar  * Ciechanover, A. The unravelling of the ubiquitin system. _Nat. Rev. Mol. Cell Biol._ 16,

322–324 (2015). Article  CAS  Google Scholar  * Bondeson, D. P. et al. Catalytic in vivo protein knockdown by small-molecule PROTACs. _Nat. Chem. Biol._ 11, 611–617 (2015). Article  CAS 

Google Scholar  * Winter, G. E. et al. Drug development. Phthalimide conjugation as a strategy for in vivo target protein degradation. _Science_ 348, 1376–1381 (2015). Article  CAS  Google

Scholar  * Jiang, Y. H. et al. Development of stabilized peptide-based PROTACs against estrogen receptor alpha. _Acs Chem. Biol._ 13, 628–635 (2018). Article  CAS  Google Scholar  * Xing,

Y., Clements, W. K., Kimelman, D. & Xu, W. Crystal structure of a beta-catenin/axin complex suggests a mechanism for the beta-catenin destruction complex. _Genes Dev._ 17, 2753–2764

(2003). Article  CAS  Google Scholar  * Ghandi, M. et al. Next-generation characterization of the cancer cell line encyclopedia. _Nature_ 569, 503–508 (2019). Article  CAS  Google Scholar  *

Huang, S. M. et al. Tankyrase inhibition stabilizes axin and antagonizes Wnt signalling. _Nature_ 461, 614–620 (2009). Article  CAS  Google Scholar  * Ye, P. et al. Tankyrases maintain

homeostasis of intestinal epithelium by preventing cell death. _PLoS Genet._ 14, e1007697 (2018). Article  Google Scholar  * Fearon, E. R. & Vogelstein, B. A genetic model for colorectal

tumorigenesis. _Cell_ 61, 759–767 (1990). Article  CAS  Google Scholar  * Tuveson, D. & Clevers, H. Cancer modeling meets human organoid technology. _Science_ 364, 952–955 (2019).

Article  CAS  Google Scholar  * Liu, Y. & Chen, Y. G. 2D-based and 3D-based intestinal stem cell cultures for personalized medicine. _Cells_ 7, E225 (2018). Article  Google Scholar  *

Sato, T. et al. Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche. _Nature_ 459, 262–265 (2009). Article  CAS  Google Scholar  * Simonetta, K. R. et

al. Prospective discovery of small molecule enhancers of an E3 ligase-substrate interaction. _Nat. Commun._ 10, 1402 (2019). Article  Google Scholar  * Li, V. S. et al. Wnt signaling through

inhibition of beta-catenin degradation in an intact Axin1 complex. _Cell_ 149, 1245–1256 (2012). Article  CAS  Google Scholar  * Hon, W. C. et al. Structural basis for the recognition of

hydroxyproline in HIF-1 alpha by pVHL. _Nature_ 417, 975–978 (2002). Article  CAS  Google Scholar  * Min, J. H. et al. Structure of an HIF-1alpha -pVHL complex: hydroxyproline recognition in

signaling. _Science_ 296, 1886–1889 (2002). Article  CAS  Google Scholar  * Bird, G. H. et al. Hydrocarbon double-stapling remedies the proteolytic instability of a lengthy peptide

therapeutic. _Proc. Natl Acad. Sci. USA_ 107, 14093–14098 (2010). Article  CAS  Google Scholar  * Dietrich, L. et al. Cell permeable stapled peptide inhibitor of Wnt signaling that targets

beta-catenin protein–protein interactions. _Cell Chem. Biol._ 24, 958–968 e955 (2017). Article  CAS  Google Scholar  * Li, Y. et al. Discovery of MD-224 as a first-in-class, highly potent,

and efficacious proteolysis targeting chimera murine double minute 2 degrader capable of achieving complete and durable tumor regression. _J. Med Chem._ 62, 448–466 (2019). Article  CAS 

Google Scholar  * Zhao, B. et al. The non-muscle-myosin-II heavy chain Myh9 mediates colitis-induced epithelium injury by restricting Lgr5+ stem cells. _Nat. Commun._ 6, 7166 (2015). Article

  CAS  Google Scholar  * Wang, Y. et al. Single-cell transcriptome analysis reveals differential nutrient absorption functions in human intestine. _J. Exp. Med._ 272, e20191130 (2019).

Google Scholar  Download references ACKNOWLEDGEMENTS We thank Dr. Wei Wu for _APC__min/+_ mice and MSAB, Qiaoni Shi, Yuzhen Li and Yuan Liu for technical assistance. This work was supported

by grants from the National Key Research and Development Program of China (2017YFA0103601 to YGC and 2017YFA0505200 To L.L.) and the National Natural Science Foundation of China (31330049 to

YGC, 91753205 to L.L. and 91849129 to H.G.H.). AUTHOR INFORMATION Author notes * These authors contributed equally: Hongwei Liao, Xiang Li, Lianzheng Zhao AUTHORS AND AFFILIATIONS * The

State Key Laboratory of Membrane Biology, Tsinghua-Peking Center for Life Sciences, School of Life Sciences, Tsinghua University, 100084, Beijing, China Hongwei Liao, Lianzheng Zhao, Yalong

Wang, Xiaodan Wang & Ye-Guang Chen * School of Pharmacy, Second Military Medical University, 200433, Shanghai, China Xiang Li, Ye Wu & Hong-Gang Hu * Department of General Surgery,

Peking University Third Hospital, Beijing, China Xin Zhou & Wei Fu * Tsinghua-Peking Center for Life Sciences, Department of Chemistry, Tsinghua University, 100084, Beijing, China Lei

Liu * Institute of Translational Medicine, Shanghai University, 200444, Shanghai, China Hong-Gang Hu Authors * Hongwei Liao View author publications You can also search for this author

inPubMed Google Scholar * Xiang Li View author publications You can also search for this author inPubMed Google Scholar * Lianzheng Zhao View author publications You can also search for this

author inPubMed Google Scholar * Yalong Wang View author publications You can also search for this author inPubMed Google Scholar * Xiaodan Wang View author publications You can also search

for this author inPubMed Google Scholar * Ye Wu View author publications You can also search for this author inPubMed Google Scholar * Xin Zhou View author publications You can also search

for this author inPubMed Google Scholar * Wei Fu View author publications You can also search for this author inPubMed Google Scholar * Lei Liu View author publications You can also search

for this author inPubMed Google Scholar * Hong-Gang Hu View author publications You can also search for this author inPubMed Google Scholar * Ye-Guang Chen View author publications You can

also search for this author inPubMed Google Scholar CONTRIBUTIONS H.L. and Y.G.C. designed the experiments; X.L., L.L., and H.H. designed the PROTACs; Y.W. and X.L. synthesized the PROTACs;

H.L., L.Z., and Y.W. performed the experiments; X.Z. and W.F. collected the CRC samples; X.W. performed bioinformatic analysis; H.L. and Y.G.C. analyzed the data; H.L., X.L., Y.W., and

Y.G.C. wrote the paper. CORRESPONDING AUTHORS Correspondence to Hong-Gang Hu or Ye-Guang Chen. ETHICS DECLARATIONS CONFLICT OF INTEREST The authors declare that they have no conflict of

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THIS ARTICLE CITE THIS ARTICLE Liao, H., Li, X., Zhao, L. _et al._ A PROTAC peptide induces durable β-catenin degradation and suppresses Wnt-dependent intestinal cancer. _Cell Discov_ 6, 35

(2020). https://doi.org/10.1038/s41421-020-0171-1 Download citation * Received: 31 December 2019 * Accepted: 24 April 2020 * Published: 09 June 2020 * DOI:

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