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Metastasis-suppressing NID2, an epigenetically-silenced gene, in the pathogenesis of nasopharyngeal carcinoma and esophageal squamous cell carcinoma

机译:鼻咽癌和食管鳞状细胞癌发病机制中抑制转移的表观遗传沉默基因NID2

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摘要

Nidogen-2 (NID2) is a key component of the basement membrane that stabilizes the extracellular matrix (ECM) network. The aim of the study is to analyze the functional roles of NID2 in the pathogenesis of nasopharyngeal carcinoma (NPC) and esophageal squamous cell carcinoma (ESCC). We performed genome-wide methylation profiling of NPC and ESCC and validated our findings using the methylation-sensitive high-resolution melting (MS-HRM) assay. Results showed that promoter methylation of NID2 was significantly higher in NPC and ESCC samples than in their adjacent non-cancer counterparts. Consistently, down-regulation of NID2 was observed in the clinical samples and cell lines of both NPC and ESCC. Re-expression of NID2 suppresses clonogenic survival and migration abilities of transduced NPC and ESCC cells. We showed that NID2 significantly inhibits liver metastasis. Mechanistic studies of signaling pathways also confirm that NID2 suppresses the EGFR/Akt and integrin/FAK/PLCγ metastasis-related pathways. This study provides novel insights into the crucial tumor metastasis suppression roles of NID2 in cancers.
机译:Nidogen-2(NID2)是基底膜的关键成分,可稳定细胞外基质(ECM)网络。本研究的目的是分析NID2在鼻咽癌(NPC)和食道鳞状细胞癌(ESCC)发病中的功能。我们对NPC和ESCC进行了全基因组甲基化分析,并使用甲基化敏感的高分辨率熔解(MS-HRM)分析验证了我们的发现。结果显示,NPC和ESCC样品中NID2的启动子甲基化明显高于其相邻的非癌对应物。一致地,在NPC和ESCC的临床样品和细胞系中观察到NID2的下调。 NID2的重新表达抑制了转导的NPC和ESCC细胞的克隆形成存活和迁移能力。我们表明,NID2显着抑制肝转移。信号通路的机制研究也证实NID2抑制EGFR / Akt和整联蛋白/ FAK /PLCγ转移相关通路。这项研究提供了对NID2在癌症中至关重要的肿瘤转移抑制作用的新见解。

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