Stromal modulation to prevent resistance

Stromal modulation to prevent resistance

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Access through your institution Buy or subscribe Intrinsic resistance to chemotherapy in pancreatic ductal adenocarcinoma (PDA) has been attributed to stromal components, such as activated pancreatic stellate cells (PSCs). Sherman _et al_. found that activation of the vitamin D receptor (VDR) can convert PSCs to a quiescent state. The VDR ligand calcipotriol induced transcriptional reprogramming of PSCs and stromal remodelling. Furthermore, in a mouse model of PDA, treatment with calcipotriol plus gemcitabine increased delivery of gemcitabine to tumours and significantly improved survival compared with gemcitabine alone. This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs * Contact customer support REFERENCES * Sherman, M. H. et al. Vitamin D receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy. _Cell_ 159, 80–93 (2014) Article  CAS  PubMed  PubMed Central  Google Scholar  Download references Authors * Sarah Seton-Rogers View author publications You can also search for this author inPubMed Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Seton-Rogers, S. Stromal modulation to prevent resistance. _Nat Rev Cancer_ 14, 707 (2014). https://doi.org/10.1038/nrc3855 Download citation * Published: 24 October 2014 * Issue Date: November 2014 * DOI: https://doi.org/10.1038/nrc3855 SHARE THIS ARTICLE Anyone you share the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer Nature SharedIt content-sharing initiative

Access through your institution Buy or subscribe Intrinsic resistance to chemotherapy in pancreatic ductal adenocarcinoma (PDA) has been attributed to stromal components, such as activated


pancreatic stellate cells (PSCs). Sherman _et al_. found that activation of the vitamin D receptor (VDR) can convert PSCs to a quiescent state. The VDR ligand calcipotriol induced


transcriptional reprogramming of PSCs and stromal remodelling. Furthermore, in a mouse model of PDA, treatment with calcipotriol plus gemcitabine increased delivery of gemcitabine to tumours


and significantly improved survival compared with gemcitabine alone. This is a preview of subscription content, access via your institution ACCESS OPTIONS Access through your institution


Subscribe to this journal Receive 12 print issues and online access $209.00 per year only $17.42 per issue Learn more Buy this article * Purchase on SpringerLink * Instant access to full


article PDF Buy now Prices may be subject to local taxes which are calculated during checkout ADDITIONAL ACCESS OPTIONS: * Log in * Learn about institutional subscriptions * Read our FAQs *


Contact customer support REFERENCES * Sherman, M. H. et al. Vitamin D receptor-mediated stromal reprogramming suppresses pancreatitis and enhances pancreatic cancer therapy. _Cell_ 159,


80–93 (2014) Article  CAS  PubMed  PubMed Central  Google Scholar  Download references Authors * Sarah Seton-Rogers View author publications You can also search for this author inPubMed 


Google Scholar RIGHTS AND PERMISSIONS Reprints and permissions ABOUT THIS ARTICLE CITE THIS ARTICLE Seton-Rogers, S. Stromal modulation to prevent resistance. _Nat Rev Cancer_ 14, 707


(2014). https://doi.org/10.1038/nrc3855 Download citation * Published: 24 October 2014 * Issue Date: November 2014 * DOI: https://doi.org/10.1038/nrc3855 SHARE THIS ARTICLE Anyone you share


the following link with will be able to read this content: Get shareable link Sorry, a shareable link is not currently available for this article. Copy to clipboard Provided by the Springer


Nature SharedIt content-sharing initiative