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TMEM16A在结肠癌组织中的表达及其意义 被引量:4

Significance of TMEM16A expression in colorectal carcinoma
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摘要 目的:探讨Ca2+激活的氯离子通道(Ca2+-activated Cl-channels,CaCC)蛋白TMEM16A在结肠癌中的表达和意义.方法:收集67例结肠癌标本,采用免疫组织化学SP法检测TMEM16A的表达,以癌旁结肠黏膜组织和6例结肠腺瘤组织作为对照,1例胃间质瘤组织作为阳性对照.结果:TMEM16A表达于结肠癌细胞胞膜和胞质内,在67例结肠癌中TMEM16A呈不同程度阳性表达,其中阴性占5.97%(4/67)、弱阳性占16.42%(11/67)、阳性占29.85%(20/67)、强阳性占47.76%(32/67);在癌旁结肠黏膜腺体内大多呈阴性和弱阳性表达,其中阴性占40.30%(27/67)、弱阳性占52.24%(35/67)、阳性占4.48%(3/67)、强阳性占2.99%(2/67);在6例结肠腺瘤中均呈阳性表达.将阴性和弱阳性表达分为阴性组,将阳性和强阳性表达分为阳性组进行分析,在67例结肠癌中TMEM16A表达的总阳性率("阳性"和"强阳性")占77.61%(52/67),而在相应的癌旁组织中TMEM16A表达的总阳性率("阳性"和"强阳性")仅占7.46%(5/67),两者之间差异显著(P<0.005).结论:TMEM16A可高表达于结肠癌组织,可作为结肠癌的分子诊断和靶向治疗的一个新的候选靶点. AIM:To investigate the expression of transmembrane protein 16A (TMEM16A) in colorectal carcinoma. METHODS:The expression of TMEM16A was detected by immunohistochemistry in 67 surgical colorectal carcinoma specimens and matched tumor-adjacent colorectal specimens. RESULTS:TMEM16A was expressed in both cytoplasm and cell membrane. Among 67 colorectal carcinoma specimens, TMEM16A expression was negative in 4 cases (5.97%), weakly positive in 11 cases (16.42%), positive in 20 cases (29.85%), and strongly positive in 32 cases (47.76%). Among 67 tumor-adjacent healthy tissue specimens, TMEM16A expression was negative in 27 cases (40.30%), weakly positive in 35 cases (52.24%), positive in 3 cases (4.48%), and strongly positive in 2 cases (2.99%). The positive ("positive" plus "strongly positive") rate of TMEM16A expression was significantly higher in colorectal carcinoma tissue than in tumor adjacent healthy tissue (77.61% vs 7.46%, P 0.005). CONCLUSION:Aberrant expression of TMEM16A is a frequent feature in colorectal carcinoma. TMEM16A can be used as a new candidate target for diagnosis and treatment of colorectal carcinoma.
出处 《世界华人消化杂志》 CAS 北大核心 2012年第35期3464-3469,共6页 World Chinese Journal of Digestology
基金 国家自然科学基金资助项目 No.NNSFC30872403 教育部新世纪优秀人才计划基金资助项目 No.NCET-10-0647 教育部"长江学者和创新团队发展计划"创新团队基金资助项目 No.IRT1171~~
关键词 结肠癌 Ca2+激活的氯离子通道 TMEM16A 免疫组织化学 Colorectal carcinoma Ca2+-activated Cl-channels TMEM16A Immunohistochemistry
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  • 1才保加,祁玉娟,周为,王晓龙.结肠腺癌患者癌组织中TPX2、PTEN和Ki67的关系及临床意义[J].中国老年学杂志,2014,34(9):2399-2401. 被引量:5
  • 2王大庆,罗清礼.眼睑基底细胞癌与其相关基因的研究进展[J].国际眼科杂志,2007,7(4):1131-1134. 被引量:2
  • 3Amanda J. Harvey,Caroline J. Pennington,Sarah Porter,Rajpal S. Burmi,Dylan R. Edwards,William Court,Suzanne A. Eccles,Mark R. Crompton.Brk Protects Breast Cancer Cells from Autophagic Cell Death Induced by Loss of Anchorage[J]. The American Journal of Pathology . 2009 (3)
  • 4Lin SW, Ke FC, Hsiao PW, et al. Critical involvement of ILK in TGFbetal - stimulated invasion/migration of human o- varian cancer cells is associated with urokinase plasminogen acti- vator system [J]. Exp Cell Res,2007,313 ( 3 ) : 602 - 613.
  • 5Hanzu FA, Gasa R, Bulur N, et al. Expression of TMEM16A and SLC4A4 in human pancreatic islets [J]. Cell Physiol Biochem, 2012,29 ( 1 - 2 ) :61 - 64.
  • 6Yao X, Li D, Xiong DM, et al. A novel role of ribonu- clease inhibitor in regulation of epithelial - to - mesenchymal transition and ILK signaling pathway in bladder cancer cells [J]. Cell Tissue Res,2013,353(3) :409 -423.
  • 7Liu W, Lu M, Liu B, et al. Inhibition of Ca (2 + ) - activated C1 (-) channel ANO1/TMEM16A expression sup- presses tumor growth and invasiveness in human prostate carci- noma[J]. Cancer Lett,2012,326( 1 ) :41 -51.
  • 8Li J, Yang ZL, Ren X, et al. ILK and PRDX1 are prognostic markers in squamous cell/adenosquamous carcinomas and adenocarcinoma of gallbladder [J]. Tumour Biol, 2013,34 ( 1 ) :359 -368.
  • 9Engelman Mde F, Grande RM, Naves MA, et al. Inte- grin- linked kinase (ILK)expression correlates with tumor se- verity in clear cell renal? carcinoma [J]. Pathol Oncol Res, 2013,19 ( 1 ) :27 - 33.
  • 10Albasri A, A1 - Ghamdi S, Fadhil W, et al. Cten sig- nals through integrin -linked kinase(ILK) and may promote me- tastasis in colorectal cancer[J]. Oncogene ,2011,30 (26):2997 - 3002.

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