期刊文献+

结直肠癌中PAQR3甲基化水平及mRNA表达的研究 被引量:3

The methylation and m RNA expression of PAQR3 in colorectal cancer
下载PDF
导出
摘要 目的研究结直肠癌组织中抑癌基因PAQR3 mRNA表达情况及甲基化水平,探讨PAQR3基因异常甲基化与结直肠癌的关系。方法收集结直肠癌及正常组织标本54组,用逆转录-聚合酶链反应(RT-PCR)检测结直肠癌标本中PAQR3 mRNA表达水平;用甲基化特异性聚合酶链反应(MSP)法检测结直肠癌标本中PAQR3基因甲基化水平,用以分析PAQR3甲基化水平与临床病理资料的关系。结果 54组结直肠癌标本中PAQR3 mRNA表达降低发生率为57.4%(31/54),正常组织PAQR3 mRNA表达降低发生率为18.5%(10/54),表达差异有统计学意义(P=0.000);癌组织PAQR3基因启动子甲基化发生率为33.3%(18/54),正常组织PAQR3基因启动子甲基化率为5.6%(3/54),二者差异有统计学意义(P=0.000);PAQR3基因甲基化与年龄、分化程度、浸润深度、临床分期、淋巴结转移有关,与性别、部位无关。结论结直肠癌组织中PAQR3表达降低,与其基因启动子发生高甲基化有关。 Objective To investigate the relationship between the methylation level of PAQR3 and colorectal cancer, the methylation level and mRNA expression of PAQR3 gene in colorectal cancer were detected. Methods 54 colorectal cancers and 54 colorectal normal tissues were collected to detect the expression of mRNA level by reverse transcriptase PCR(RT-PCR), the methylation level of PAQR3 gene were detected by Methylation Specific PCR(MSP), which were used to analyze the relationship between methylation of PAQR3 and clinical data. Results Expression of PAQR3 mRNA in 54 normal tissues were significantly higher than that in 54 colorectal cancer tissues, the expression rates were 18.5%(10/54) and 57.4%(31/54), there was significant difference between cancer and normal tissues(P= 0.000).The PAQR3 gene promoter methylation rate of colorectal cancer and colorectal normal tissues were 33.3%(18/54)and 5.6 %(3/54), there was significant difference between cancer and normal tissues(P= 0.000).There was significant difference in age, differentiation, infiltration, clinical stage and the metastasis of lymph node in colorectal cancer, but not in sex and location. Conclusion PAQR3 expression can be reduced in colorectal cancer, PAQR3 gene promoter hypermethylation may play an important role in oncogenesis of colorectal cancer.
出处 《医学研究与教育》 CAS 2015年第1期55-60,共6页 Medical Research and Education
关键词 PAQR3 结直肠癌 甲基化 MSP PAQR3 colorectal cancer methylation MSP
  • 相关文献

参考文献11

  • 1JAVIER C F, AZUARA D, BERENGUER-LLERGO A, et al. DNA methylation biomarkers for noninvasive diagnosis of colorectal cancer[J]. Cancer Prevention Research, 2013, 6(7): 656-665.
  • 2HENRI S T, DANIEL M C, MICHAEL B D, et al. Nutritional factors and gender influence age-related DNA methylation in the human rectal mucosa[J]. Aging Cell, 2013, 12(1): 148-155.
  • 3XIE Xiaoduo, ZHANG Yixuan, JIANG Yuhui, et al. Suppressive function of RKTG on chemical carcinogen-induced skin carcinogenesis in mouse[J]. Carcinogenesis, 2008, 29(8): 1632-1638.
  • 4FENG Lin, XIE Xiaoduo, DING Qiurong, et al. Spatial regulation of Raf kinase signaling by RKTG[J]. Proc Natl Acad Sci USA, 2007, 104(36): 14348-14353.
  • 5CANO E, MAHADEVAN L C. Parallel signal processing among mammalian MAPKs[J]. Trends Biochem Sci, 1995, 20(3): 117- 122.
  • 6FAN Fengjuan, FENG Lin, HE Jing, et al. RKTG sequesters B-Raf to the Golgi apparatus and inhibits the proliferation and tumorigenicity of human malignant melanoma cells[J]. Carcinogenesis, 2008, 29(6): 1157-1163.
  • 7WANG Xiao, LI Xuebing, FAN Fengjuan, et aL PAQR3 plays a suppressive role in the tumorigenesis of eolorectal cancers[J]. Carcinogenesis, 2012, 33 (11): 2228-2235.
  • 8陈雁,谢小多.RKTG基因功能研究[J].细胞生物学杂志,2009,31(1):9-14. 被引量:3
  • 9黄剑波,罗鑫荣,孔令泉,向廷秀,任国胜.PAQR3增强乳腺癌细胞SK-BR-3的表柔比星敏感性[J].第三军医大学学报,2013,35(16):1658-1662. 被引量:3
  • 10LILLYCROP K A, HOILE S P, GRENFELL L, et al. DNA methylation, ageing and the influence of early life nutrition[J]. Proceedings of the Nutrition Society, 2014, 73(3): 413-421.

二级参考文献59

  • 1刘碧清,熊绍权,王柏丁.肠复康对人大肠癌HT-29细胞增殖的影响及作用机制研究[J].肿瘤防治研究,2004,31(12):759-761. 被引量:3
  • 2夏光涛,张源潮,武森森,张尚忠.NDGA对HT-29结肠癌细胞生长抑制及对端粒酶表达影响的研究[J].中国肿瘤生物治疗杂志,2005,12(4):262-265. 被引量:1
  • 3王立伟,陈丽新,钟平,聂思槐,曾广华,唐慰萍,罗经文,余忠华.平阳霉素和普鲁卡因治疗鼻咽癌时细胞膜电位的变化[J].中国病理生理杂志,1996,12(3):249-253. 被引量:3
  • 4Zhu Y, Rice CD, Pang Y, et al. Cloning, expression, and characterization of a membrane progestin receptor and evidence it is an intermediary in meiotic maturation of fish oocytes, Proc Natl Acad Sci USA, 2005, 100(5): 2231-2236.
  • 5Thomas, P. Characteristics of membrane progestin receptor alpha (mPRalpha) and progesterone membrane receptor component 1 (PGMRC1) and their roles in mediating rapid progestin actions, Front Neuroendocrinol, 2008, 29(2): 292-312.
  • 6Feng L, Xie X, Ding Q, et al. Spatial regulation of Raf kinase signaling by RKTG, Proc Natl Acad Sci USA, 2007, 104(36): 14348-14353.
  • 7Fan F, Feng L, He J, et al. RKTG sequesters B-Raf to the Golgi apparatus and inhibits the proliferation and tumorigenicity of human malignant melanoma cells, Carcinogenesis, 2008, 29 (6): 1157-1163.
  • 8Xie X, Zhang Y, Jiang Y, et al. Suppressive function of RKTG on chemical carcinogen-induced skin carcinogenesis in mouse. Carcinogenesis, 2008, 29(8): 1632-1638.
  • 9Cano E, Mahadevan LC. Parallel signal processing among mammalian MAPKs, Trends Biochem Sci, 20(3): 117-122.
  • 10Harding A, Tian T, Westbury E, et al. Subcellular localization determines MAP kinase signal output, Curr Biol, 2005, 15(9): 869-873.

共引文献4

同被引文献42

  • 1Yoshimitsu Akiyama.Methylation of GATA-4 and GATA-5 and development of sporadic gastric carcinomas[J].World Journal of Gastroenterology,2010,16(10):1201-1208. 被引量:9
  • 2Feng L, Xie X, Ding Q, et al. Spatial regulation of Raf ki- nase signaling by RKTG[J]. Proc Natl Acad Sci USA, 2007, 104(36): 14348-14353.
  • 3Garitaonandia I, Smith JL, Kupchak BR, etal. Adiponectin identified as an agonist for PAQR3/RKTG using a yeast- based assay system[J]. J Recept Signal Transduct Res, 2009, 29(1): 67-73.
  • 4Zhang Y, Jiang X, Qin X, et al. RKTG inhibits angiogenesis by suppressing MAPK-mediated autocrine VEGF signaling and is downregulated in clear-cell renal cell carcinoma[J]. Oncogene, 2010, 29(39): 5404-5415.
  • 5Liu C, Zhang Y, Hou Y, et al, PAQR3 modulates H3K4 tri- methylation by spatial modulation of the regulatory sub-units of COMPASS-like complexes in mammalian cells[J]. Biochem J, 2015, 467(3): 415-424.
  • 6Wang L, Wang X, Li Z, et al. PAQR3 has modulatory roles in obesity, energy metabolism, and leptin signaling[J]. En- docrinology, 2013, 154(12): 4525-4535.
  • 7Wang X, Wang L, Zhu L, et al. PAQR3 modulates insulin signaling by shunting phosphoinositide 3-kinase p110c~ to the Golgi apparatus[J]. Diabetes, 2013, 62(2): 444-456.
  • 8Jiang Y, Xie X, Li Z, et al. Functional cooperation of RK- TG with p53 in tumorigenesis and epithelial-mesenchymal transition[J]. Cancer Res, 2011, 71(8): 2959-2968.
  • 9Fan F, Feng L, He J, et al. RKTG sequesters B-Raf to the Golgi apparatus and inhibits the proliferation and tumorige nicity of human malignant melanoma cells[J]. Carcinogenesis, 2008, 29(6): 1157-1163.
  • 10Xie X, Zhang Y, Jiang Y, et al. Suppressive function of RK- TG on chemical carcinogen-induced skin carcinogenesis in mouse[J]. Carcinogenesis, 2008, 29(8): 1632-1638.

引证文献3

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部