Fijneman Remond J A, Cormier Robert T
Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Front Biosci. 2008 May 1;13:4144-74. doi: 10.2741/2998.
The mouse secretory phospholipase A2 group IIA (sPLA2-IIA) gene Pla2g2a has been identified as a susceptibility gene for cancer of the small and large intestine. Interestingly, unlike most previously identified tumor susceptibility genes, Pla2g2a does not behave like a classical oncogene or tumor suppressor gene. Hence, identification of its biological functions in tumor development may shed new light on general mechanisms that modulate colon cancer risk. So far, sPLA2-IIA has been proposed to play a role in anti-bacterial defense, inflammation and eicosanoid generation, in clearance of apoptotic cells, and in the Wnt signaling pathway. More recently, comparison of RNA expression profiles of colon from Pla2g2a-transgenic to Pla2g2a-deficient mice confirmed and even extended sPLA2-IIA's diverse biological effects. In this review we aim to summarize current knowledge about the various links of sPLA2-IIA to cancer of the gastro-intestinal tract, and propose several models to illustrate its putative biological effects on tumor development.
小鼠分泌型磷脂酶A2第二亚家族A组(sPLA2-IIA)基因Pla2g2a已被确定为小肠和大肠癌症的一个易感基因。有趣的是,与大多数先前鉴定的肿瘤易感基因不同,Pla2g2a的行为不像经典的癌基因或肿瘤抑制基因。因此,确定其在肿瘤发生中的生物学功能可能会为调节结肠癌风险的一般机制提供新的线索。到目前为止,sPLA2-IIA已被认为在抗菌防御、炎症和类花生酸生成、凋亡细胞清除以及Wnt信号通路中发挥作用。最近,对Pla2g2a转基因小鼠和Pla2g2a基因缺陷小鼠结肠的RNA表达谱进行比较,证实并进一步扩展了sPLA2-IIA的多种生物学效应。在这篇综述中,我们旨在总结目前关于sPLA2-IIA与胃肠道癌症各种联系的知识,并提出几种模型来说明其对肿瘤发生的假定生物学效应。