School of Biological Sciences, Nanyang Technological University, 60 Nanyang Drive, Singapore 637551, Singapore.
Cancer Cell. 2011 Mar 8;19(3):401-15. doi: 10.1016/j.ccr.2011.01.018.
Cancer is a leading cause of death worldwide. Tumor cells exploit various signaling pathways to promote their growth and metastasis. To our knowledge, the role of angiopoietin-like 4 protein (ANGPTL4) in cancer remains undefined. Here, we found that elevated ANGPTL4 expression is widespread in tumors, and its suppression impairs tumor growth associated with enhanced apoptosis. Tumor-derived ANGPTL4 interacts with integrins to stimulate NADPH oxidase-dependent production of O(2)(-). A high ratio of O(2)(-):H(2)O(2) oxidizes/activates Src, triggering the PI3K/PKBα and ERK prosurvival pathways to confer anoikis resistance, thus promoting tumor growth. ANGPTL4 deficiency results in diminished O(2)(-) production and a reduced O(2)(-):H(2)O(2) ratio, creating a cellular environment conducive to apoptosis. ANGPTL4 is an important redox player in cancer and a potential therapeutic target.
癌症是全球主要的死亡原因。肿瘤细胞利用各种信号通路来促进其生长和转移。据我们所知,血管生成素样蛋白 4(ANGPTL4)在癌症中的作用尚未确定。在这里,我们发现升高的 ANGPTL4 表达广泛存在于肿瘤中,其抑制会损害与增强凋亡相关的肿瘤生长。肿瘤衍生的 ANGPTL4 与整合素相互作用,刺激 NADPH 氧化酶依赖性 O(2)(-)的产生。高比例的 O(2)(-):H(2)O(2)氧化/激活Src,触发 PI3K/PKBα 和 ERK 生存促进途径,赋予抗失巢凋亡能力,从而促进肿瘤生长。ANGPTL4 缺乏会导致 O(2)(-)产生减少和 O(2)(-):H(2)O(2)比值降低,创造有利于细胞凋亡的环境。ANGPTL4 是癌症中重要的氧化还原调节剂,也是潜在的治疗靶点。