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

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 genom...

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Detalles Bibliográficos
Autores principales: Chai, Annie Wai Yeeng, Cheung, Arthur Kwok Leung, Dai, Wei, Ko, Josephine Mun Yee, Ip, Joseph Chok Yan, Chan, Kwok Wah, Kwong, Dora Lai-Wan, Ng, Wai Tong, Lee, Anne Wing Mui, Ngan, Roger Kai Cheong, Yau, Chun Chung, Tung, Stewart Yuk, Lee, Victor Ho Fun, Lam, Alfred King-Yin, Pillai, Suja, Law, Simon, Lung, Maria Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346683/
https://www.ncbi.nlm.nih.gov/pubmed/27793011
http://dx.doi.org/10.18632/oncotarget.12889
Descripción
Sumario: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.