TY - JOUR
T1 - Hedgehog signaling restrains bladder cancer progression by eliciting stromal production of urothelial differentiation factors
AU - Shin, Kunyoo
AU - Lim, Agnes
AU - Zhao, Chen
AU - Sahoo, Debashis
AU - Pan, Ying
AU - Spiekerkoetter, Edda
AU - Liao, Joseph C.
AU - Beachy, Philip A.
N1 - Funding Information:
This research was supported in part by grants from the NIH to P.A.B., and J.C.L. and a Pathway to Independence Award (K99/R00) to K.S. P.A.B. is an investigator of the Howard Hughes Medical Institute.
Publisher Copyright:
© 2014 Elsevier Inc.
PY - 2014/10/13
Y1 - 2014/10/13
N2 - Hedgehog (Hh) pathway inhibitors are clinically effective in treatment of basal cell carcinoma and medulloblastoma, but fail therapeutically or accelerate progression in treatment of endodermally derived colon and pancreatic cancers. In bladder, another organ of endodermal origin, we find that despite its initial presence in the cancer cell of origin Sonic hedgehog (Shh) expression is invariably lost during progression to invasive urothelial carcinoma. Genetic blockade of stromal response to Shh furthermore dramatically accelerates progression and decreases survival time. This cancer-restraining effect of Hh pathway activity is associated with stromal expression of BMP signals, which stimulate urothelial differentiation. Progression is dramatically reduced by pharmacological activation of BMP pathway activity with low-dose FK506, suggesting an approach to management of human bladder cancer.
AB - Hedgehog (Hh) pathway inhibitors are clinically effective in treatment of basal cell carcinoma and medulloblastoma, but fail therapeutically or accelerate progression in treatment of endodermally derived colon and pancreatic cancers. In bladder, another organ of endodermal origin, we find that despite its initial presence in the cancer cell of origin Sonic hedgehog (Shh) expression is invariably lost during progression to invasive urothelial carcinoma. Genetic blockade of stromal response to Shh furthermore dramatically accelerates progression and decreases survival time. This cancer-restraining effect of Hh pathway activity is associated with stromal expression of BMP signals, which stimulate urothelial differentiation. Progression is dramatically reduced by pharmacological activation of BMP pathway activity with low-dose FK506, suggesting an approach to management of human bladder cancer.
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U2 - 10.1016/j.ccell.2014.09.001
DO - 10.1016/j.ccell.2014.09.001
M3 - Article
C2 - 25314078
AN - SCOPUS:84907996793
SN - 1535-6108
VL - 26
SP - 521
EP - 533
JO - Cancer Cell
JF - Cancer Cell
IS - 4
ER -