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子宫颈癌组织XIAP蛋白表达及其意义 被引量:2

The expression and significance of X-linked inhibitor of apoptosis protein in cervical carcinoma tissues
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摘要 目的:探讨XIAP蛋白表达在子宫颈癌发生、发展过程中的作用,以及XIAP蛋白表达与子宫颈癌患者的年龄、癌细胞分化程度、病理分期和淋巴转移之间的关系。方法:通过HE染色从组织病理学确定子宫颈组织的良、恶性以及恶性组织的分级和分期,应用免疫组织化学SP法检测65例子宫颈癌组织和24例慢性子宫颈炎组织中XIAP蛋白的表达情况。结果:①慢性子宫颈炎组织XIAP蛋白表达的阳性率为37.50%,低于子宫颈癌组织中的73.85%,两者比较差异有统计学意义(P<0.01)。②子宫颈癌组织XIAP蛋白表达随分化程度降低而升高(P<0.01),有淋巴转移的患者高于无淋巴转移的患者(P<0.05);子宫颈癌组织XIAP蛋白表达与患者年龄、病理分期无关(P>0.05)。结论:XIAP蛋白在子宫颈癌组织中表达水平明显升高,提示它与子宫颈癌发生、发展有密切关系,子宫颈癌组织XIAP蛋白表达水平的差异,对子宫颈癌的病理诊断及其分级有参考价值,干扰XIAP的表达可用于子宫颈癌的治疗。 Objective : To explore the effect of X - linked inhibitor of apoptosis protein (XIAP) on the occurrence and development of cervical carcinoma and the relationship between XIAP expression and age, cancer cell differentiation degree, pathologic staging and lymphatic metastasis. Methods: HE staining was used to determine whether the cervix tissue was benign or malignant and definite the grading and staging of the malignant tissues histopathologically. The expression level of XIAP protein in 65 cases of cervical carcinoma tissue and 24 cases of chronic cervicitis tissue were detected by Immunohistochemical staining. Results : The positive rate of XIAP protein in chronic cervicitis tissue was 37.50%, which was lower than that (73.85%) in cervical cancer tissue (P 〈 0. 01 ) ; The XIAP protein expression in cervical carcinoma tissue increased with the decline of cancer cells differentiation degree (P 〈 0. 01 ), and the expression level of XIAP protein was higher in the patients with lymphatic metastasis than those without lymphatic metastasis ( P 〈 0. 05 ) ; there was no correlation between XIAP protein expression and age, clinical staging ( P 〉 0.05 ) . Conclusion: The up - regulation of XIAP protein cervical carcinoma tissue indicates that XIAP is related to the occurrence and development of cervical carcinoma. The difference of XIAP protein expression level in cervical carcinoma tissue can serve as a valuable reference for the pathological diagnosis and grading of cervical carcinoma. It is implied that interfering with XIAP expression could be used to treat cervical carcinoma.
出处 《中国妇幼保健》 CAS 北大核心 2009年第19期2715-2718,共4页 Maternal and Child Health Care of China
关键词 子宫颈癌 XIAP 免疫组织化学 Cervical carcinoma X - linked inhibitor of apoptosis protein immunohistochemistry
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  • 1Lewis J, Burstein E, Reffey SB, et al . Uncoupling of the signaling and caspase-inhibitory properties of X-linked inhibitor of apoptosis[J]. J Biol Chem ,2004, 279(10) : 9023-9029.
  • 2Shiraki K, Sugimoto K, Yamanaka Y, et al. Overexpression of X-linked inhibitor of apoptosis in human hepatocellular carcinoma[J]. Int J Mol Med ,2003,12(5):705-708.
  • 3Berezovskaya O, Schimmer AD, Glinskii AB, et al . Increased expression of apoptosis inhibitor protein XIAP contributes to anoikis resistance of circulating human prostate cancer metastasis precursor cells[J]. Cancer Res ,2005, 65(6) :2378.
  • 4Ramp U, Krieg T, Caliskan E, et al . XIAP expression is an independent prognostic marker in clear-cell renal carcinomas [J]. Hum Pathol ,2004, 35(8):1022-1028.
  • 5Lee YK, Bone ND, Strege AK, et al . VEGF Receptor phosphorylation status and apoptosis is modulated by a green tea component, epigallocatechin-3-gallate (EGCG) in B cell chronic lymphocytic leukemia[J]. Blood , 2004, 104 (3):788-794.
  • 6Hofmann HS, Simm A, Hammer A, et al . Expression of inhibitor of apoptosis (IAP) proteins in non-small cell human lung cancer[J]. J Cancer Res Clin Oncol , 2002, Oct; 128 (10) :554-560.
  • 7Peter L, Natalie R, Katsuyukl T, et al. Suppression of apoptosis in mammalian cells by NAPI and a related family of IAP genes[J]. Nature ,1996, 379(15) : 349-353.
  • 8Yamaguchi K, Nagai S, Ninomiya-Tsuji J, et al . XIAP, a cellular member of the inhibitor of apoptosis protein family, links the receptors to TAB1-TAK1 in the BMP signaling pathway[J]. EMBO J , 2002, 18(1):179-187.
  • 9Yang L, Cao Z, Yan H, et al. Coexistence of high levels of apoptotic signaling and inhibitor of apoptosis proteins in human tumor cells: implication for cancer specific therapy[J]. Cancer Res , 2003, 63(20) :6815-6824.
  • 10Rajcan-Separovic E,Liston P,Lefebvre C,et al. Assignment of human inhibitor of apoptosis protein (IAP) genes xiap, hiap-1 and hiap-2 to chromosomes Xq25 and 11 q22-q23 by fluorescence in situ hybridization [ J ]. Genomics, 1996 ;37 ( 3 ) :404-6.

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  • 1周琳,杨期东,袁梦石,马志健,侯德仁,谭兴林.何首乌对淀粉样β蛋白致海马神经元的凋亡和学习记忆障碍的作用[J].中国临床康复,2005,9(9):131-133. 被引量:11
  • 2张曙光,刘芝华,张林.凋亡抑制基因XIAP在肿瘤治疗中的研究进展[J].世界华人消化杂志,2006,14(26):2626-2631. 被引量:6
  • 3潘军华,张志,韩培彦.BMP-2在口腔医学领域的研究与应用[J].北京口腔医学,2006,14(4):300-301. 被引量:2
  • 4Perez-Cruz C,Nolte MW,van Gaalen MM,et al.Reduced spine density in specific regions of CA1 pyramidal neurons in two transgenic mouse models of Alzheimer's disease.J Neurosci,2011,31:3926-3934.
  • 5Deveraux QL,Takahashi R,Salvesen GS,et al.X-linked IAP is a direct inhibitor of cell-death proteases.Nature,1997,388:300-304.
  • 6Kilic U,Kilic E,Dietz GP,et al.Intravenous TAT-GDNF is protective after focal cerebral ischemia in mice.Stroke,2003,34:1304-1310.
  • 7Mancxak M,Anekonda TS,Henson E,et al.Mitochondria are a direct site of Aβ accumulation in ALzheimer' s disease neurons:implications for free radical generation and oxidative damage in disease progression.Hum Mol Genet,2006,15:1437-1449.
  • 8Burguillos MA,Deierborg T,Kavanagh E,et al.Caspase signalling controls microglia activation and neurotoxicity.Nature,2011,472:319-324.
  • 9Zhu C,Xu F,Fukuda A,et al.X chromosome-linked inhibitor of apoptosis protein reduces oxidative stress after cerebral irradiation or hypoxia-ischemia through up-regulation of mitochondrial antioxidants.Eur J Neurosci,2007,26:3402-3410.
  • 10Doeppner TR,Dietz GP,E1 Aanbouri M,et al.TAT-Bcl-x(L) improves survival of neuronal precursor cells in the lesioned striatum after focal cerebral ischemia.Neurobiol Dis,2009,34:87-94.

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