Denicola Gina, Tuveson David A
Department of Cancer Biology, Abramson Family Cancer Research Institute, The Abramson Cancer Center at the University of Pennsylvania Medical Center, Philadelphia, PA, USA.
Cancer Biol Ther. 2005 May;4(5):509-11. doi: 10.4161/cbt.4.5.1781. Epub 2005 May 2.
Pancreatic ductal adenocarcinoma (PDA) is arguably the most lethal malignancy in the United States. Despite the identification of many molecular alterations in PDA, this information has not translated into effective therapeutic strategies to date. A recent report in Cancer Cell (Fernandez-Zapico et al, Cancer Cell 2005, 7:39-49) reveals an unexpected role for the hematopoietic-specific RhoGEF VAV1 in pancreatic tumorigenesis, where ectopic expression of VAV1 as a result of promoter demethylation was identified in the majority of established cell lines and PDA tissue samples. Importantly, VAV1 expression was functionally required for optimal proliferation, transformation and survival of pancreatic cancer cell lines. This study provides the first evidence of VAV1 promoter demethylation as an event in cancer progression, suggesting that aberrant signaling pathways driven by VAV1 are potential therapeutic targets in PDA.
胰腺导管腺癌(PDA)可以说是美国最致命的恶性肿瘤。尽管已经确定了PDA中的许多分子改变,但迄今为止,这些信息尚未转化为有效的治疗策略。《癌细胞》杂志最近的一篇报道(费尔南德斯 - 萨皮科等人,《癌细胞》2005年,7卷:39 - 49页)揭示了造血特异性RhoGEF VAV1在胰腺肿瘤发生中的一个意想不到的作用,其中在大多数已建立的细胞系和PDA组织样本中,由于启动子去甲基化而鉴定出VAV1的异位表达。重要的是,VAV1表达对于胰腺癌细胞系的最佳增殖、转化和存活在功能上是必需的。这项研究提供了VAV1启动子去甲基化作为癌症进展事件的首个证据,表明由VAV1驱动的异常信号通路是PDA潜在的治疗靶点。