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CLN3基因在卵巢浆液性囊腺癌中的表达及耐药相关性的研究

CLN3 gene expression in ovarian serous cystadenocarcinoma and drug-resistant correlation research
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摘要 目的探讨CLN3(青少年神经元腊样质脂褐质沉积症Juvenile,form of neuronalceroid-lipofuscinosis,JNCL,Batten病)基因在卵巢浆液性囊腺癌中的表达特点及其在卵巢癌化疗耐药中的作用。方法采用半定量RT-PCR、Western blot以及免疫组化的方法检测CLN3在卵巢浆液性囊腺癌中的表达,分析其表达与临床病理特征及化疗耐药的相关性。结果 CLN3在卵巢浆液性囊腺癌中的表达高于正常卵巢组织,且临床分期越晚其表达越高(P<0.05),而与肿瘤患者年龄无显著相关性。CLN3在卵巢癌化疗耐药组表达阳性率明显高于化疗敏感组(P<0.05)。结论卵巢癌中CLN3高表达与卵巢癌的发生、发展、浸润和转移有关,与卵巢癌化疗耐药密切相关。CLN3可成为卵巢癌化疗新的基因治疗靶点。 Objective:Explore CLN3 gene expression in ovarian serous cystadenocarcinoma characteristics and its role in ovarian cancer chemotherapy drug resistance. Methods:Using semi-quantitative RT-PCR. Western blot and immunohistochemical method to detect CLN3 expression in ovarian serous cystadenocarcinoma,analyze its expression and the clinical pathology characteristic and the correlation of chemotherapy drug resistance. Results:CLN3 expression in ovarian serous cystadenocarcinoma is higher than normal ovarian tissue and the longer the higher expression and the clinical stages(P﹤0.05),and there was no significant correlation with tumor patients age. CLN3 expression positive rate in ovarian cancer chemotherapy drug resistance group was obviously higher than that of chemotherapy sensitivity group. Conclusion:CLN3 high expression in ovarian cancer and ovarian cancer occurrence,development,invasion and metastasis,closely associated with ovarian cancer chemotherapy drug resistance. CLN3 can be as a new gene therapy targets ovarian cancer chemotherapy.
出处 《中国优生与遗传杂志》 2015年第10期13-15,F0004,共4页 Chinese Journal of Birth Health & Heredity
基金 黑龙江省教育厅科学技术研究项目 项目编号11551161
关键词 CLN3基因 卵巢浆液性囊腺癌 临床病理特征 化疗耐药 CLN3 Clinical pathological features Ovarian serous cystadenocarcinoma Chemotherapy drug resistance
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参考文献8

  • 1Dey S, Soliman AS.Cancer in the global health era :opportunities for the Middle East and Asia[J].Asia Pac J Public Health, 2010, 22 (3 Suppl) :75S-82S.
  • 2Ferlay J, Parkin D M, Steliarova-Foucher E. Estimates of cancer incidence and mortality in Europe in 2008[J].Eur J Cancer, 2010, 46 (4) :765-781.
  • 3胡琼,李维山,郑洪.卵巢浆液性肿瘤中凋亡调控因子Smac Caspase-9和Caspase-3的表达及意义[J].中国肿瘤临床,2007,34(9):497-500. 被引量:7
  • 4The International Batten Disease Consortium. Isolation of anovel gene underlying Batten disease[J]. Cell, 1995, 82 (3) ..949-957.
  • 5连丽娟,刘彤华,等.林巧稚妇科肿瘤学[M].第三版.人民卫生出版社,2000.426.
  • 6Robert J, Morgan JR, Ronald D, et al.Ovarian cancer including Fallopian tube cancer and Primary peritoneal cancer[M]. NCCN clinical practice guidelines in ontology, 2009, (2).
  • 7Vlao Q, Foster BJ, Xia H, et al. Membrane topology of CLN3, the protein underlying Batten disease[J].FEBS Lett, 2003, 541 (1-3) : 40-46.
  • 8Kasturi LP, Wei-Xing G, Wei-Hua Q, et al. CLN3 defines a novel antipoptotic pathway operative in neurodegenera -tion and mediated by ceramide[J].Mol Genet Metab, 1999, 66 (2) :294-308.

二级参考文献10

  • 1郑洪,杨光华,周桥.横纹肌肉瘤中凋亡抑制蛋白c-IAP1、c-IAP2和sur-vivin的表达及意义[J].临床与实验病理学杂志,2003,19(2):141-144. 被引量:5
  • 2Reed JC. Mechanisms of apoptosis [J]. Am J Padaol, 2000, 157(5): 1415~1430.
  • 3Fu J, Jin Y, Arend LJ. Smac3, a novel Smac/DIABLO splicing variant, attenuates the stability and apoptosis-inhibiting activity of X-linked inhibitor of apoptosis protein[J]. J Biol Chem, 2003, 278 (52): 52660~52672.
  • 4McNeish IA, Bell S, McKay T, et al. Expression of Smac/DIABLO in ovarian carcinoma cells induces apoptosis via a caspase-9-mediated pathway[J]. Exp Cell Res, 2003, 286(2): 186~198.
  • 5Hengarmer MO. The biochemistry of apoptosis [J]. Nature, 2000, 407(6805): 770~776.
  • 6Cain K, Bratton SB, Langlais C, et al. Apaf-1 oligomerizes into biologically acdve approximately 700-kDa and inactive approxi- mately 1.4-MDa apoptosorne complexes [J].J Biol Chem, 2000, 275(9): 6067~6070.
  • 7Tringler B, Lehner R, Shroyer AL, et al. Immunohistochemical localization of survivin in serous tumors of the ovary [J]. Appl Immunolfistochem Mol Morphol, 2004, 12(1): 40~43.
  • 8Janicke RU, Sprengart ML, Wati MR, et al. Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis[J].J Biol Chem, 1998, 273(16): 9357~9360.
  • 9Soengas MS, Alarcon RM, Yoshida H, et al. Apaf-1 and caspase-9 in p53-dependent apoptosis and tumor inhibidon [J]. Science, 1999, 284(5411): 156~159.
  • 10Fiskum G, Mitochondrial participation in ischemic and traumatic neural cell death[J]. J Neurotrauma, 2000, 17(10):843~855.

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