Department of Surgery, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Division of Advanced Surgical Oncology, Department of Research and Development Center for New Medical Frontiers, Kitasato University School of Medicine, Sagamihara, Kanagawa, Japan.
Ann Surg Oncol. 2019 Feb;26(2):406-414. doi: 10.1245/s10434-018-6865-z. Epub 2018 Oct 11.
Cysteine dioxygenase type 1 (CDO1) acts as a tumor suppressor gene, and its expression is regulated by promoter DNA methylation in human cancer. The metabolic product mediated by CDO1 enzyme increases mitochondrial membrane potential (MMP), putatively representing chemoresistance. The aim of this study is to investigate the functional relevance of CDO1 gene in colon cancer with chemotherapy.
We investigated 170 stage III colon cancer patients for CDO1 methylation by using quantitative methylation-specific polymerase chain reaction (PCR). To elucidate the functional role of CDO1 gene in colorectal cancer (CRC) biology, we established cell lines that stably express CDO1 gene and evaluated chemosensitivity, MMP, and tolerability assay including anaerobic environment.
Hypermethylation of CDO1 gene was an independent prognostic factor for stage III colon cancer on multivariate prognostic analysis. Surprisingly, patients with CDO1 hypermethylation exhibited better prognosis than those with CDO1 hypomethylation in stage III colon cancer with postoperative chemotherapy (P = 0.03); however, a similar finding was not seen in those without postoperative chemotherapy. In some CRC cell lines, forced expression of CDO1 gene increased MMP accompanied by chemoresistance and/or tolerance under hypoxia.
CDO1 methylation may be a useful biomarker to increase the number of stage III colon cancer patients who can be saved by adjuvant therapy. Such clinical relevance may represent the functionally oncogenic property of CDO1 gene through MMP activity.
半胱氨酸双加氧酶 1(CDO1)作为一种肿瘤抑制基因,其表达受人类癌症启动子 DNA 甲基化的调控。CDO1 酶介导的代谢产物增加线粒体膜电位(MMP),推测代表化疗耐药性。本研究旨在探讨 CDO1 基因在结肠癌化疗中的功能相关性。
我们通过定量甲基化特异性聚合酶链反应(PCR)检测了 170 例 III 期结肠癌患者的 CDO1 甲基化情况。为了阐明 CDO1 基因在结直肠癌(CRC)生物学中的功能作用,我们建立了稳定表达 CDO1 基因的细胞系,并评估了化疗敏感性、MMP 和耐受性试验,包括厌氧环境。
CDO1 基因的高甲基化是 III 期结肠癌多因素预后分析的独立预后因素。令人惊讶的是,在接受术后化疗的 III 期结肠癌患者中,CDO1 高甲基化患者的预后优于 CDO1 低甲基化患者(P=0.03);然而,在未接受术后化疗的患者中未发现类似的结果。在一些 CRC 细胞系中,CDO1 基因的强制表达增加了 MMP,同时在缺氧条件下还伴有化疗耐药性和/或耐受性。
CDO1 甲基化可能是一种有用的生物标志物,可以增加接受辅助治疗的 III 期结肠癌患者的数量。这种临床相关性可能代表了 MMP 活性通过 CDO1 基因的功能致癌特性。