The prognostic significance and therapeutic potential of hedgehog signaling in intrahepatic cholangiocellular carcinoma.


PURPOSE The correlation of the hedgehog signaling pathway with the progression, prognosis, and therapeutics of intrahepatic cholangiocellular carcinoma (ICC) has not been well documented. The study aimed to investigate the expression, prognostic significance, and therapeutic value of hedgehog components in ICC. EXPERIMENTAL DESIGN Two independent cohorts of 200 patients with ICC were enrolled. By real-time PCR and immunohistochemistry assay, hedgehog components expression was evaluated. The prognostic values of hedgehog proteins were identified and verified. Cyclopamine or siRNA-targeting Gli was used to block the hedgehog signaling. Cell proliferation and apoptosis were observed by CCK8, cell cycle, and annexin V staining assays. In vivo murine tumor model was used to evaluate the role of hedgehog in ICC. RESULTS In ICC tissues, the Gli1 nuclear immune-intensity was associated with intrahepatic metastasis and the expression of Gli2 was associated with intrahepatic metastasis, venous invasion, and Unio Internationale Contra Cancrum (UICC) pT characteristics. In survival analysis, high Gli1 or Gli2 expressers had an unfavorable overall survival (OS) prognosis and a shorter disease-free survival (DFS) than those with low expression. In multivariate analysis, Gli1 expression was found to be an independent prognostic factor of OS, which was validated by another independent cohort. Furthermore, blocking the hedgehog signaling by cyclopamine or siRNA-targeting Gli1 resulted in apoptosis and growth inhibition in ICC cells. CONCLUSIONS This study shows, for the first time, activation of hedgehog pathway associated with the progression and metastasis in ICC, which may provide prognostic and therapeutic values for this tumor.

DOI: 10.1158/1078-0432.CCR-12-0349

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@article{Tang2013ThePS, title={The prognostic significance and therapeutic potential of hedgehog signaling in intrahepatic cholangiocellular carcinoma.}, author={Liang Tang and Ye-xiong Tan and Bei-ge Jiang and Yu-fei Pan and Shuang-xi Li and Guang-zhen Yang and Min Wang and Qing Wang and Jian Zhang and Weiping Zhou and Li-wei Dong and Hong-Yang Wang}, journal={Clinical cancer research : an official journal of the American Association for Cancer Research}, year={2013}, volume={19 8}, pages={2014-24} }