Department of Cancer and Cell Biology, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, USA.
J Biol Chem. 2012 Apr 27;287(18):14792-802. doi: 10.1074/jbc.M112.347625. Epub 2012 Mar 6.
The multifunctional caspase-2 protein is involved in apoptosis, NF-κB regulation, and tumor suppression in mice. However, the mechanisms of caspase-2 responsible for tumor suppression remain unclear. Here we identified two sites of caspase-2, the catalytic Cys-320 site and the Ser-139 site, to be important for suppression of cellular transformation and tumorigenesis. Using SV40- and K-Ras-transformed caspase-2 KO mouse embryonic fibroblast cells reconstituted with expression of wild-type, catalytic dead (C320A), or Ser-139 (S139A) mutant caspase-2, we demonstrated that similar to caspase-2 deficiency, when Cys-320 and Ser-139 were mutated, caspase-2 lost its ability to inhibit cellular transformation and tumorigenesis. These mutant cells exhibited enhanced cell proliferation, elevated clonogenic activity, accelerated anchorage-independent growth, and transformation and were highly tumorigenic, rapidly producing large tumors in athymic nude mice. Investigation into the underlying mechanism showed that these two residues are needed for caspase-2 to suppress NF-κB activity, promote apoptosis, and sustain the G(2)/M checkpoint following DNA damage induction. In addition, tumors in nude mice derived from the two mutant cell lines had higher constitutive NF-κB activity and elevated expression of NF-κB targets of antiapoptotic proteins Bcl-xL, XIAP, and cIAP2. A reduction in caspase-2 mRNA was associated with multiple types of cancers in patients. Together, these observations suggest the combined functions of caspase-2 in suppressing NF-κB activation, promoting apoptosis, and sustaining G(2)/M checkpoint contribute to caspase-2 tumor-suppressing function and that caspase-2 may also impact tumor suppression in humans. These findings provide insight into tumor suppression at the cross-roads of apoptosis, cell cycle checkpoint, and NF-κB pathways.
多功能半胱天冬酶-2 蛋白参与细胞凋亡、NF-κB 调节和小鼠肿瘤抑制。然而,半胱天冬酶-2 负责肿瘤抑制的机制尚不清楚。在这里,我们鉴定了半胱天冬酶-2 的两个位点,即催化半胱氨酸-320 位点和丝氨酸-139 位点,对于抑制细胞转化和肿瘤发生非常重要。使用 SV40 和 K-Ras 转化的半胱天冬酶-2 KO 小鼠胚胎成纤维细胞,用野生型、催化失活(C320A)或丝氨酸-139(S139A)突变半胱天冬酶-2 表达重建,我们证明,与半胱天冬酶-2 缺陷类似,当半胱氨酸-320 和丝氨酸-139 发生突变时,半胱天冬酶-2 丧失抑制细胞转化和肿瘤发生的能力。这些突变细胞表现出增强的细胞增殖、升高的集落形成活性、加速的无锚定生长和转化,并具有高度的致瘤性,在免疫缺陷裸鼠中迅速产生大肿瘤。对潜在机制的研究表明,这两个残基对半胱天冬酶-2 抑制 NF-κB 活性、促进细胞凋亡以及在 DNA 损伤诱导后维持 G2/M 检查点是必需的。此外,来自这两个突变细胞系的裸鼠肿瘤具有更高的组成性 NF-κB 活性和抗凋亡蛋白 Bcl-xL、XIAP 和 cIAP2 的 NF-κB 靶标的上调表达。在患者中,与多种类型的癌症相关的是 caspase-2 mRNA 的减少。总之,这些观察结果表明,半胱天冬酶-2 在抑制 NF-κB 激活、促进细胞凋亡和维持 G2/M 检查点方面的综合功能有助于半胱天冬酶-2 的肿瘤抑制功能,并且半胱天冬酶-2 也可能影响人类的肿瘤抑制。这些发现为细胞凋亡、细胞周期检查点和 NF-κB 途径交汇处的肿瘤抑制提供了新的见解。