期刊文献+

皮肤鳞状细胞癌组织中p16及14-3-3σ基因启动子甲基化检测及其相关性分析 被引量:3

Analyses of p16 and 14-3-3σ promoter methylation, and their association with skin squamous cell carcinoma
原文传递
导出
摘要 目的:通过检测皮肤鳞状细胞癌组织及正常皮肤组织中p16及14-3-3σ基因启动子甲基化,探讨p16及14-3-3σ基因启动子甲基化在皮肤鳞状细胞癌发生发展中的作用。方法:实时荧光定量聚合酶链反应(q-PCR)法检测53例皮肤鳞状细胞癌组织及48例正常皮肤组织中p16和14-3-3σm RNA表达,免疫印迹(western blot)法检测p16和14-3-3σ蛋白表达,应用甲基化特异性PCR对所提DNA进行p16及14-3-3σ基因启动子甲基化检测,并分析这两个基因的相关性。结果:皮肤鳞状细胞癌标本中p16及14-3-3σm RNA表达均低于正常皮肤组织,皮肤鳞状细胞癌标本中p16和14-3-3σ蛋白亦低于正常皮肤组织,皮肤鳞状细胞癌标本中p16及14-3-3σ基因启动子甲基化的阳性率分别为54.72%(29/53)和67.92%(36/53),高于对照组的8.33%(4/48)和18.75(9/48),差异有统计学意义(P<0.001);皮肤鳞状细胞癌组织中p16和14-3-3σ的甲基化存在正相关关系(r=0.431,χ~2=9.825,P=0.002,P<0.05)。结论:皮肤鳞状细胞癌标本中p16及14-3-3σ低表达及甲基化与鳞状细胞癌发生发展可能有关,皮肤鳞状细胞癌基因启动子甲基化可能是多位点参与的。 Objective: To compare p16 and 14-3-3σ gene promoter methylation in skin squamous cell carcinoma (SCC) with that in normal skin, and to investigate pathogenic roles of these methylations in squamous cell carcinoma. Methods: SCC specimens from 53 patients and normal skin tissues from 48 individuals were used to assess the expression levels of p16 and 14-3-3σ proteins and mRNA, using Western blot and real-time fluorescence-based quantitative PCR, respectively. Methylation-specific PCR was used to assess promoter methylation of p16 and 14-3-3σ genes. Correlations between p16 or 14-3-3σ methylation and clinicopathological parameters were analyzed with the Spearman rank test. Results: SCC specimens showed significantly lower levels of both p16/14-3-3σ mRNA and protein compared to normal skin. In contrast, promoter methylation rates of p16and 14-3-3σ were significantly higher in SCC than in normal skin(p16:54.72% vs. 8.33%; 14-3- 3σ: 67.92% vs. 18.75%, both P〈0.001). Methylation rates of p16 and 14-3-3σ genes in SCCs displayed positive correlation (r=0.431, X^2=9.825, P=0.002). Conclusions: The low expression levels, and methylations of p16 and 14-3-3σ genes may play pathogenic roles in SCC, and gene promoter methylations at multiple sites may be involved in SCC.
出处 《临床皮肤科杂志》 CSCD 北大核心 2017年第12期835-839,共5页 Journal of Clinical Dermatology
基金 若干皮肤病性病省内诊疗体系建设与转化医学研究基金(BL2012007)资助项目
关键词 皮肤鳞状细胞癌 P16基因启动子 14—3—3σ基因启动子 甲基化 squamous cell carcinoma p16 promoter 14-3-3σ promoter methylation
  • 相关文献

参考文献3

二级参考文献12

  • 1齐淑贞,王千秋,谈玉,沈艳,李波,陈淑丽,程刚,秦红友,尤志学,周兵斌.测序法及液相芯片杂交法对生殖道人乳头瘤病毒感染分型的比较[J].中国医学科学院学报,2007,29(2):181-185. 被引量:8
  • 2Dlugosz A, Merlino G, Yuspa. SH. Progress in cutaneous cancer research[J]. J Investig Dermatol Symp Proc, 2002, 7(1):17-26.
  • 3Liggett WH Jr, Sidransky D. Role of the p16 tumor suppressor gene in cancer[J]. J Clin Oncol, 1998, 16(3): 1197-1206.
  • 4Al-Mohanna MA, Manogaran PS, Al-Mukhalafi Z, et al. The tumor suppressor p16(INK4a) gene is a regulator of apoptosis induced by ultraviolet light and cisplatin[J]. Oncogene, 2004, 23(1): 201-212.
  • 5Gonzalez-Zulueta M, Bender CM, Yang AS, et al. Methylation of the 5' CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silenc ing[J]. Cancer Res, 1995, 55(20): 4531-4535.
  • 6Ehrhart JC, Gosselet FP, Culerrier RM, et al. UVB-induced mutations in human key gatekeeper genes governing signaling pathways and consequences for skin tumourigenesis [J]. Photochem Photobiol Sci, 2003, 2(8): 825-834.
  • 7Brown VL, Harwood CA, Crook T, et al. p16INK4a and p14ARF tumor suppressor genes are commonly inactivated in cutaneous squamous cell carcinoma[J]. J Invest Dermatol, 2004, 122(5):1284-1292.
  • 8Saridaki Z, Liloglou T, Zafiropoulos A, et al. Mutational analysis of CDKN2A genes in patients with squamous cell carcinoma of the skin[J]. Br J Dermatol, 2003, 148(4): 638-648.
  • 9Blokx WA, de Jong EM, de Wilde PC, et al. P16 and p53 expression in (pre)malignant epidermal tumors of renal transplant recipients and immunocompetent individuals [J]. Mod Pathol,2003, 16(9): 869-878.
  • 10Green CL, Khavari PA. Targets for molecular therapy of skin cancer[J]. Semin Cancer Biol, 2004, 14:63-69.

共引文献5

同被引文献28

引证文献3

二级引证文献3

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