Tgf-β signalling regulator pmepa1 halts metastases to bone

feature-image

Play all audios:

    

Access through your institution Buy or subscribe New research, published in _Cancer Cell_, has shown that PMEPA1 inhibits TGF-β signalling by a nonproteasomal mechanism and that knockdown of


PMAPA1 increases prometastatic gene expression and bone metastases in a mouse model. TGF-β is a critical regulator of cell proliferation and differentiation and that it has a complex role


is cancer is well known. Fournier and colleagues sort to characterize the role of TGF-β signalling and regulated genes in the development of bone metastases in prostate cancer. 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 * Fournier, P. G. J. _ et al_. The TGF-β


signalling regulator PMEPA1 suppresses prostate cancer to bone. _Cancer Cell_ 10.1016/j.ccell.2015.04.009 Download references Authors * Louise Stone 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 Stone, L. TGF-β signalling regulator PMEPA1 halts


metastases to bone. _Nat Rev Urol_ 12, 362 (2015). https://doi.org/10.1038/nrurol.2015.136 Download citation * Published: 09 June 2015 * Issue Date: July 2015 * DOI:


https://doi.org/10.1038/nrurol.2015.136 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