Sun Yat-sen University Cancer Center, State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Guangzhou, 510060, China.
Department of Colorectal Surgery, Sun Yat-sen University Cancer Center, Guangzhou, 510060, China.
Oncogene. 2021 Dec;40(49):6680-6691. doi: 10.1038/s41388-021-02052-5. Epub 2021 Oct 13.
Colorectal carcinoma (CRC) is the second most deadly cancer worldwide. Therapies that take advantage of DNA repair defects have been explored in various tumors but not yet systematically in CRC. Here, we found that Diphosphoinositol Pentakisphosphate Kinase 2 (PPIP5K2), an inositol pyrophosphate kinase, was highly expressed in CRC and associated with a poor prognosis of CRC patients. In vitro and in vivo functional studies demonstrated that PPIP5K2 could promote the proliferation and migration ability of CRC cells independent of its inositol pyrophosphate kinase activity. Mechanically, S1006 dephosphorylation of PPIP5K2 could accelerate its dissociation with 14-3-3 in the cytoplasm, resulting in more nuclear distribution. Moreover, DNA damage treatments such as doxorubicin (DOX) or irradiation (IR) could induce nuclear translocation of PPIP5K2, which subsequently promoted homologous recombination (HR) repair by binding and recruiting RPA70 to the DNA damage site as a novel scaffold protein. Importantly, we verified that S1006 dephosphorylation of PPIP5K2 could significantly enhance the DNA repair ability of CRC cells through a series of DNA repair phenotype assays. In conclusion, PPIP5K2 is critical for enhancing the survival of CRC cells via facilitating DNA HR repair. Our findings revealed an unrecognized biological function and mechanism model of PPIP5K2 dependent on S1006 phosphorylation and provided a potential therapeutic target for CRC patients.
结直肠癌(CRC)是全球第二大致命癌症。利用 DNA 修复缺陷的疗法已在各种肿瘤中进行了探索,但尚未在 CRC 中系统地进行。在这里,我们发现二磷酸肌醇 pentakisphosphate 激酶 2(PPIP5K2),一种肌醇五磷酸激酶,在 CRC 中高度表达,并与 CRC 患者的预后不良相关。体外和体内功能研究表明,PPIP5K2 可以促进 CRC 细胞的增殖和迁移能力,而不依赖其肌醇五磷酸激酶活性。在机制上,PPIP5K2 的 S1006 去磷酸化可以加速其与细胞质中 14-3-3 的解离,导致更多的核分布。此外,DNA 损伤处理,如阿霉素(DOX)或辐射(IR),可以诱导 PPIP5K2 的核易位,随后通过与 RPA70 结合并募集到 DNA 损伤部位作为一种新型支架蛋白,促进同源重组(HR)修复。重要的是,我们通过一系列 DNA 修复表型测定验证了 PPIP5K2 的 S1006 去磷酸化可以显著增强 CRC 细胞的 DNA 修复能力。总之,PPIP5K2 通过促进 DNA HR 修复,对增强 CRC 细胞的存活至关重要。我们的发现揭示了 PPIP5K2 依赖 S1006 磷酸化的一个未被认识的生物学功能和机制模型,并为 CRC 患者提供了一个潜在的治疗靶点。