DiFeo Analisa, Narla Goutham, Martignetti John A
Mount Sinai School of Medicine, New York, NY, USA.
Mt Sinai J Med. 2009 Dec;76(6):557-66. doi: 10.1002/msj.20150.
Epithelial ovarian cancer is one of the most lethal gynecologic cancers and the fifth most frequent cause of female cancer deaths in the United States. Despite dramatic treatment successes in other cancers through the use of molecular agents targeted against genetically defined events driving cancer development and progression, very few insights into epithelial ovarian cancer have been translated from the laboratory to the clinic. If advances are to be made in the early diagnosis, prevention, and treatment of this disease, it will be critical to characterize the common and private (personalized) genetic defects underlying the development and spread of epithelial ovarian cancer. The tumor suppressor Kruppel-like factor 6 and its alternatively spliced, oncogenic isoform, Kruppel-like factor 6 splice variant 1, are members of the Kruppel-like zinc finger transcription factor family of proteins, which have diverse roles in cellular differentiation, development, proliferation, growth-related signal transduction, and apoptosis. Inactivation of Kruppel-like factor 6 and overexpression of Kruppel-like factor 6 splice variant 1 have been associated with the progression of a number of human cancers and even with patient survival. This article summarizes our recent findings demonstrating that a majority of epithelial ovarian cancer tumors have Kruppel-like factor 6 allelic loss and decreased expression coupled with increased expression of Kruppel-like factor 6 splice variant 1. The targeted reduction of Kruppel-like factor 6 in ovarian cancer cell lines results in marked increases in cell proliferation, invasion, tumor growth, angiogenesis, and intraperitoneal dissemination in vivo. In contrast, the inhibition of Kruppel-like factor 6 splice variant 1 decreases cellular proliferation, invasion, angiogenesis, and tumorigenicity; this provides the rationale for its potential therapeutic application. These results and our recent demonstration that the inhibition of Kruppel-like factor 6 splice variant 1 can dramatically prolong survival in a preclinical mouse model of ovarian cancer are reviewed and discussed.
上皮性卵巢癌是最致命的妇科癌症之一,也是美国女性癌症死亡的第五大常见原因。尽管通过使用针对驱动癌症发展和进展的基因定义事件的分子药物,在其他癌症的治疗方面取得了巨大成功,但从实验室到临床,对上皮性卵巢癌的了解却非常有限。如果要在这种疾病的早期诊断、预防和治疗方面取得进展,那么表征上皮性卵巢癌发生和扩散背后的常见和个体(个性化)基因缺陷至关重要。肿瘤抑制因子Kruppel样因子6及其选择性剪接的致癌异构体Kruppel样因子6剪接变体1是Kruppel样锌指转录因子家族蛋白的成员,它们在细胞分化、发育、增殖、生长相关信号转导和细胞凋亡中具有多种作用。Kruppel样因子6的失活和Kruppel样因子6剪接变体1的过表达与多种人类癌症的进展甚至患者生存有关。本文总结了我们最近的研究结果,表明大多数上皮性卵巢癌肿瘤存在Kruppel样因子6等位基因缺失和表达降低,同时Kruppel样因子6剪接变体1的表达增加。在卵巢癌细胞系中靶向降低Kruppel样因子6会导致体内细胞增殖、侵袭、肿瘤生长、血管生成和腹腔播散显著增加。相反,抑制Kruppel样因子6剪接变体1会降低细胞增殖、侵袭、血管生成和致瘤性;这为其潜在的治疗应用提供了理论依据。本文对这些结果以及我们最近证明抑制Kruppel样因子6剪接变体1可显著延长卵巢癌临床前小鼠模型的生存期进行了综述和讨论。