The Sidney Kimmel Comprehensive Cancer Center, Department of Oncology, Johns Hopkins University School of Medicine, CRB245, 1650 Orleans Street, Baltimore, MD 21287, USA.
Clin Cancer Res. 2012 Sep 15;18(18):4883-8. doi: 10.1158/1078-0432.CCR-11-2509. Epub 2012 Jun 19.
The Hedgehog (Hh) signaling pathway regulates embryonic development and may be aberrantly activated in a wide variety of human cancers. Efforts to target pathogenic Hh signaling have steadily progressed from the laboratory to the clinic, and the recent approval of the Hh pathway inhibitor vismodegib for patients with advanced basal cell carcinoma represents an important milestone. On the other hand, Hh pathway antagonists have failed to show significant clinical activity in other solid tumors. The reasons for these negative results are not precisely understood, but it is possible that the impact of Hh pathway inhibition has not been adequately measured by the clinical endpoints used thus far or that aberrancies in Hh signal transduction limits the activity of currently available pathway antagonists. Further basic and correlative studies to better understand Hh signaling in human tumors and validate putative antitumor mechanisms in the clinical setting may ultimately improve the success of Hh pathway inhibition to other tumor types.
刺猬(Hh)信号通路调节胚胎发育,并且可能在多种人类癌症中异常激活。靶向致病性 Hh 信号的努力已从实验室稳步推进到临床,最近批准 Hh 通路抑制剂 vismodegib 用于治疗晚期基底细胞癌,这是一个重要的里程碑。另一方面,Hh 通路拮抗剂在其他实体瘤中并未显示出显著的临床活性。这些阴性结果的原因尚不完全清楚,但可能是迄今为止使用的临床终点未能充分衡量 Hh 通路抑制的影响,或者 Hh 信号转导的异常限制了现有通路拮抗剂的活性。进一步的基础和相关研究,以更好地了解人类肿瘤中的 Hh 信号,并在临床环境中验证潜在的抗肿瘤机制,最终可能会提高 Hh 通路抑制对其他肿瘤类型的成功率。