Stromal modulation to prevent resistance
- Select a language for the TTS:
- UK English Female
- UK English Male
- US English Female
- US English Male
- Australian Female
- Australian Male
- Language selected: (auto detect) - EN
Play all audios:

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