Department of Biochemistry and Molecular Biology (BK21 project), Medical Research Center for Bioreaction to Reactive Oxygen Species and Biomedical Science Institute, School of Medicine, Kyung Hee University, Seoul, Korea.
Hepatology. 2011 Nov;54(5):1661-78. doi: 10.1002/hep.24539.
Cyclophilin B (CypB) performs diverse roles in living cells, but its role in hepatocellular carcinoma (HCC) is largely unclear. To reveal its role in HCC, we investigated the induction of CypB under hypoxia and its functions in tumor cells in vitro and in vivo. Here, we demonstrated that hypoxia-inducible factor 1α (HIF-1α) induces CypB under hypoxia. Interestingly, CypB protected tumor cells, even p53-defective HCC cells, against hypoxia- and cisplatin-induced apoptosis. Furthermore, it regulated the effects of HIF-1α, including those in angiogenesis and glucose metabolism, via a positive feedback loop with HIF-1α. The tumorigenic and chemoresistant effects of CypB were confirmed in vivo using a xenograft model. Finally, we showed that CypB is overexpressed in 78% and 91% of the human HCC and colon cancer tissues, respectively, and its overexpression in these cancers reduced patient survival.
These results indicate that CypB induced by hypoxia stimulates the survival of HCC via a positive feedback loop with HIF-1α, indicating that CypB is a novel candidate target for developing chemotherapeutic agents against HCC and colon cancer.
亲环素 B(CypB)在活细胞中发挥多种作用,但在肝细胞癌(HCC)中的作用在很大程度上尚不清楚。为了揭示其在 HCC 中的作用,我们研究了缺氧下 CypB 的诱导及其在体外和体内肿瘤细胞中的功能。在这里,我们证明缺氧诱导因子 1α(HIF-1α)在缺氧下诱导 CypB。有趣的是,CypB 保护肿瘤细胞,甚至 p53 缺陷型 HCC 细胞,免受缺氧和顺铂诱导的细胞凋亡。此外,它通过与 HIF-1α的正反馈环来调节 HIF-1α的作用,包括血管生成和葡萄糖代谢的作用。通过异种移植模型证实了 CypB 的致瘤和化疗耐药作用。最后,我们表明 CypB 在 78%的人 HCC 和 91%的结肠癌组织中过表达,并且在这些癌症中的过表达降低了患者的生存率。
这些结果表明,缺氧诱导的 CypB 通过与 HIF-1α的正反馈环刺激 HCC 的存活,表明 CypB 是开发针对 HCC 和结肠癌的化疗药物的新候选靶标。