China Oncology ›› 2014, Vol. 24 ›› Issue (8): 568-574.doi: 10.3969/j.issn.1007-3969.2014.08.002
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CUI Jian-li, GUO Wei, GUO Yan-li, SHEN Su-peng, DONG Zhi-ming
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Abstract:
Background and purpose: RASSF10 acts as a kind of tumor suppressor in various tumor tissues, but researches in cardiac adenocarcinoma has not been reported. This study aimed to detect the methylation status and expression of Ras-association domain family 10 (RASSF10) in gastric cardia adenocarcinoma (GCA), and explore its role in occurrence and development of GCA. Methods: Methylation specific polymerase chain reaction (MSP), reverse transcription-polymerase chain reaction (RT-PCR) and immunohistochemistry method were respectively used to detect methylation status, mRNA expression and protein expression of RASSF10 in 81 GCA tissues and corresponding normal tissues.Results: The promoter methylation frequency of RASSF10 in GCA tissues (64.20%, 52/81) was significantly higher than that in corresponding normal tissues (20.99%, 17/81, P<0.05), and was closely correlated with TNM stages, differential degree and lymph node metastasis (P<0.05). RASSF10 mRNA expression in GCA tissues (0.57±0.05) was significantly lower than that in corresponding normal tissues (0.78±0.02, P<0.05), and was closely correlated with TNM stages and lymph node metastasis (P<0.05). Protein expression of RASSF10 in GCA tissues (31.10%, 26/81) was significantly lower than that in corresponding normal tissues (71.60%, 58/81, P<0.05), and was closely correlated with TNM stages, differential degree and lymph node metastasis (P<0.05). The promoter methylation frequency of RASSF10 in GCA tissues was inversely related to its protein expression.Conclusion: Inactivation of RASSF10 caused by aberrant methylation in the promoter region may be closely correlated with the GCA tumorgenesis.
Key words: Gastric cardia adenocarcinoma, Methylation, RASSF10 gene
CUI Jian-li, GUO Wei, GUO Yan-li, SHEN Su-peng, DONG Zhi-ming. Methylation status and expression of RASSF10 gene in gastric cardia adenocarcinoma[J]. China Oncology, 2014, 24(8): 568-574.
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URL: http://www.china-oncology.com/EN/10.3969/j.issn.1007-3969.2014.08.002
http://www.china-oncology.com/EN/Y2014/V24/I8/568