Department of Obstetrics and Gynecology, The Second Affiliated Hospital of Nanchang University, Nanchang 330006, China;
Chin J Cancer Res. 2013 Jun;25(3):346-53. doi: 10.3978/j.issn.1000-9604.2013.06.04.
Epithelial ovarian carcinoma (EOC) is the most common form of ovarian malignancies and the most lethal gynecologic malignancy in the United States. To date, in spite of treatment to it with the extensive surgical debulking and chemotherapy, the prognosis of EOC remains dismal. Recently, it has become increasingly clear that in many instances, the signaling and molecular players that control development are the same, and when inappropriately regulated, drive tumorigenesis and cancer development. Here, we discuss the possible involvement of Hedgehog (Hh) pathway in the cellular regulation and development of cancer in the ovaries. Using the in vitro and in vivo assays developed has facilitated the dissection of the mechanisms behind Hh-driven ovarian cancers formation and growth. Based on recent studies, we propose that the inhibition of Hh signaling may interfere with spheroid-like structures in ovarian cancers. The components of the Hh signaling may provide novel drug targets, which could be explored as crucial combinatorial strategies for the treatment of ovarian cancers.
上皮性卵巢癌(EOC)是最常见的卵巢恶性肿瘤,也是美国最致命的妇科恶性肿瘤。迄今为止,尽管采用广泛的手术去肿瘤和化疗进行治疗,EOC 的预后仍然很差。最近,越来越清楚的是,在许多情况下,控制发育的信号和分子参与者是相同的,并且当它们被不恰当地调节时,会驱动肿瘤发生和癌症发展。在这里,我们讨论 Hedgehog(Hh)途径在卵巢中癌症的细胞调节和发展中的可能作用。使用已经开发的体外和体内测定法,有助于剖析 Hh 驱动的卵巢癌形成和生长背后的机制。基于最近的研究,我们提出抑制 Hh 信号可能会干扰卵巢癌中的球体样结构。Hh 信号的组成部分可能提供新的药物靶点,这些靶点可以作为治疗卵巢癌的关键组合策略进行探索。