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nm23-H1基因遗传不稳定性和宫颈癌的相关性研究 被引量:1

Genetic instability of nm23-H1 gene in cervical cancer
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摘要 目的 分析宫颈癌及癌前病变中nm23-H1基因遗传不稳定性及其与宫颈癌临床病理特征的相关性,探讨nm23-H1基因在宫颈癌发生、发展中的作用.方法 收集手术及活检宫颈新鲜组织标本146例,包括宫颈上皮内瘤变(cervical intraepithelial neoplasia,CIN)Ⅱ~Ⅲ 级48例,宫颈鳞癌(squamous cell carcinoma,SCC)48例,慢性宫颈炎50 例.采用免疫组化技术检测nm23-H1蛋白,同时用PCR-SSCP法检测nm23-H1基因遗传不稳定性.结果 (1) nm23-H1蛋白表达率随着宫颈肿瘤的进展逐渐减弱.(2) nm23-H1 基因D17S396位点的杂合性缺失(loss of heterozysity,LOH)发生率在宫颈癌晚期较多见,而微卫星不稳定(microsatellite instability,MSI)在癌前病变及早期癌中较多见.(3) LOH的增加与nm23-H1蛋白的低表达有关,MSI对nm23-H1蛋白表达的影响不大.结论 nm23-H1基因可能参与了宫颈癌的进展及浸润转移,nm23-H1基因的MSI和 LOH可能通过不同的机制影响肿瘤进展. Objective To investigate nm23-H1 gene instability in cervical cancer and its correlation with clinical and pathological characteristics. Methods A total 146 cervical tissue samples were collected from operation and biopsy, including 48 cases of CIN Ⅱ~Ⅲ, 48 cases of SCC, 50 cases of chronic cervicitis. The nm23-H1 proteins were detected by immunohistochemical method. The nm23-H1 gene instability (include LOH and MSI) were examined by PCR-SSCP. The correlation of nm23-H1 gene instability with clinical and pathological characteristics of cervical cancer were anylyzed. Results The expression of nm23-H1 protein decreased with the progressing of cervical tumor. The LOH in nm23-H1 gene was more frequent in later stage cervical cancer. MSl was more frequent in CIN and early stage cervical cancer. The increase of LOH was related to the decreased nm23-H1 protein expression. Conclusion MSI and the LOH of nm23-H1 gene are detected in cervical cancer, which may be involved in the progress in cervical cancer with different mechanicals.
出处 《浙江医学》 CAS 2011年第5期619-621,625,共4页 Zhejiang Medical Journal
基金 绍兴市科技局社会发展科研项目(2007A33007)
关键词 NM23-H1基因 遗传不稳定性 宫颈肿瘤 nm23-H1 gene Heredity instability Cervical tumor
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参考文献11

  • 1杨月琴,李继承,李小红,唐咏梅,汤新华.中国人卵巢上皮性肿瘤nm23H1基因遗传不稳定性的研究[J].实验生物学报,2005,38(3):233-240. 被引量:6
  • 2Branca M,Giorgi C,Ciotti M,et al.Down-regulated nucleoside diphosphate kinase nm23-H1 expression is unrelated to high-risk human papillomavirus but associated with progression of cervical intraepithelial neoplasia and unfavourable prognosis in cervical cancer[J].J Clin Pathol,2006,59(10):1044-1051.
  • 3Ravazoula P,Aletra C,Kourounis G,et al.Immunohistochemical analysis of nm23-H1 expression in human cervical lesions[J].Eur J Gynaecol Oncol,2000,21(5):510-512.
  • 4Wang P H,Ko J L,Chang H,et al.Clinical significance of high nm23-H1 expression in intraepithelial neoplasia and early-stage squamous cell carcinoma of the uterine cervix[J].Gynecol Obstet Invest,2003,55(1):14-19.
  • 5Wang P H,Chang H,Ko J L,et al.Nm23-H1 immunohistochemical expression In multisteps of cervical carcinogenesis[J].Int J Gynecol Cancer,2003,13(3):325-330.
  • 6Chen H Y,Hsu C T,Lin W C,et al.Prognostic value of nm23 expression in Stage IB1 cervical carcinoma[J].Jpn J Clin Oncol,2001,31(7):327-332.
  • 7International Federation of Gynecology and Obstetrics:FIGO staging of gynecologic cancers:Cervical and vulva[J].Int J Gynecol Cancer,1995,5:319-324.
  • 8Tannapful A,Kocherling F,Katalinic A,et al.Expression of nm23-H1 predicts lymph node involvement in colorectal carcinoma[J].Dis Co Pectum,1995,38(6):651-654.
  • 9Berney C R,Fisher R J,Yang J,et al.Genomic alterations (LOH,MI) on chromosome 17q21-23 and prognosis of sporadic colorectal cancer[J].Int J Cancer,2000,89(1):1-7.
  • 10Chien-Gang Hsu,Long-Yau Lin,Jiunn-Liang Ko,et al.High Expression of Human Nonmetastatic Clone 23 Type 1 in Cancer of Uterine Cervix and its Association With Poor Cell Differentiation and Worse Overall Survival[J].J Surg Oncol,2008,98(6):448-456.

二级参考文献12

  • 1Chaubert, P., N. Burri & P. Cousin, 2001,A novel highly informative polyA microsatellite on the telomeric side of the INK4a/ARF locus. MoL Cell Probes., 15:183 - 185.
  • 2Berney, C.R., R.J. Fisher, J. Yang, P.J. Russell & P.J. Crowe, 2000, Genomic alterations (LOH, MI) on chromosome 17q21-23 and prognosis of sporadic colorectal cancer. Int. J. Cancer, 89: 1-7.
  • 3Fukushima, T. & S. Takenoshita, 2001, Colorectal carcinogenesis. Fukushima J. Med. Sci., 47: 1-11.
  • 4Steeg, P.S., G. Bevilacque, L. Kopper, U.P. Thorgeirsson,JE. Talmadge, L.A. Liotta & M.E. Sobel, 1988, Evidence for a novel gene associated with tumor metastatic potential. J. Natl. Cancer Inst., 80: 200-204.
  • 5Venturelli. D., V. Cesi, S. Ransac, A. Engelhard, D.Perrotti & B. Calabretta, 2000, The nucleoside diphosphate kinase activity of DRnm23 is not required for inhibition of differentiation and induction of apoptosis in 32Dc13 myeloid precursor cells. Exp. Cell Res.,257: 265-271.
  • 6Viel, A, L. Dall'Agnese, V. Canzonieri, F. Sopracordevole, E. Capozzi, A. Carbone & MC. Visentin,1995, Suppressive role of the metastasis-related nm23H1 gene in human ovarian carcinomas : association of high messenger RNA expression with lack of lymph node metastasis. Cancer Res., 55: 2645-2650.
  • 7Alexander, J., T. Watanabe, T.T. Wu, A. Rashid, S. Li & SR. Hamilton, 2001, Histopathological identification of colon cancer with microsatellite instability. Am. J.Pathol., 158: 527-535.
  • 8Yoshida, T., T. Sugai, W. Habano, S. Nakamura, N. Uesugi, O. Funato & K. Saito, 2000, Microsatellite instability in gallbladder carcinoma: two independent genetic pathways of gallbladder carcinogenesis. J. Gastroenterol, 35: 768-774.
  • 9Kapitanovic, S., R. Spaventi, S. Vujsic, Z. Petrovic, A. Kurjak, Z.P. Pavelic, J.L. Gluckman, P.J. Stambrook & K. Pavelic, 1995, nm23-H1 gene expression in ovarian tumora-a potential tumor marker. Anticancer Res, 15:587-590.
  • 10Mandai, M., I. Konishi, T. Komatsu, T. Mori, S. Arao, H. Nomura, Y. Kanda, H. Hiai & M. Fukumoto, 1995,Mutation of the nm23 gene, loss of heterozygosity at the nm23 locus and K-ras mutation in ovarian carcinoma : correlation with tumour progression and nm23 gene expression. Br. J. Cancer, 72: 691-695.

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