Shao Luning, Cui Yan, Li Hongyu, Liu Yanan, Zhao Hongshan, Wang Yu, Zhang Yingmei, Ng Ka Man, Han Wenling, Ma Dalong, Tao Qian
Peking University Center for Human Disease Genomics, 38 [corrected] Xueynun Road, Beijing, 100083, China.
Clin Cancer Res. 2007 Oct 1;13(19):5756-62. doi: 10.1158/1078-0432.CCR-06-3082.
CMTM5 (CKLF-like MARVEL transmembrane domain containing member 5) is located at 14q11.2, a locus associated with multiple cancers. It has six RNA splicing variants with CMTM5-v1 as the major one. We explored its expression pattern in normal tissues and tumor cell lines, as well as its functions in carcinoma cells.
We evaluated CMTM5 expression by semiquantitative reverse transcription-PCR (RT-PCR) in normal tissues and carcinoma cell lines of cervical, breast, nasopharyngeal, lung, hepatocellular, esophageal, gastric, colon, and prostate. We further examined CMTM5 promoter methylation in these cell lines. We also analyzed CMTM5 expression after 5-aza-2'-deoxycytidine treatment and genetic demethylation and the functional consequences of restoring CMTM5 in HeLa and PC-3 cells.
CMTM5-v1 is broadly expressed in human normal adult and fetal tissues, but undetectable or down-regulated in most carcinoma cell lines. Its promoter methylation was detected in virtually all the silenced or down-regulated cell lines. The silencing of CMTM5 could be reversed by pharmacologic demethylation or genetic double-knockout of DNMT1 and DNMT3B, indicating methylation-mediated mechanism. Restoration of CMTM5-v1 suppressed carcinoma cell proliferation, migration, and invasion.
These results indicate that CMTM5 exhibits tumor suppressor activities, but with frequent epigenetic inactivation in carcinoma cell lines.
CMTM5(含CKLF样MARVEL跨膜结构域成员5)位于14q11.2,该位点与多种癌症相关。它有六种RNA剪接变体,其中CMTM5-v1是主要变体。我们探究了其在正常组织和肿瘤细胞系中的表达模式,以及在癌细胞中的功能。
我们通过半定量逆转录聚合酶链反应(RT-PCR)评估了CMTM5在宫颈、乳腺、鼻咽、肺、肝细胞、食管、胃、结肠和前列腺的正常组织及癌细胞系中的表达。我们进一步检测了这些细胞系中CMTM5启动子的甲基化情况。我们还分析了5-氮杂-2'-脱氧胞苷处理及基因去甲基化后CMTM5的表达,以及在HeLa和PC-3细胞中恢复CMTM5后的功能后果。
CMTM5-v1在人类正常成人及胎儿组织中广泛表达,但在大多数癌细胞系中检测不到或表达下调。几乎在所有沉默或下调的细胞系中都检测到了其启动子甲基化。CMTM5的沉默可通过药物去甲基化或DNMT1和DNMT3B的基因双敲除来逆转,表明存在甲基化介导的机制。恢复CMTM5-v1可抑制癌细胞的增殖、迁移和侵袭。
这些结果表明CMTM5具有肿瘤抑制活性,但在癌细胞系中常发生表观遗传失活。