期刊文献+

卵巢上皮癌组织中p-mTOR的表达及意义 被引量:3

Expression and clinical significance of p-mTOR in epithelial ovarian cancer
原文传递
导出
摘要 目的:探讨磷酸化的哺乳动物雷帕霉素靶蛋白(p-mTOR)在卵巢上皮癌组织中的表达和临床意义。方法:采用免疫组化方法检测154例卵巢上皮癌、25例良性上皮瘤和34例正常卵巢组织中p-mTOR蛋白表达情况,并分析其与卵巢上皮癌临床病理特征的关系。结果:p-mTOR在卵巢上皮癌组织阳性表达率为53.90%(83/154),在正常卵巢和良性卵巢上皮瘤组织中表达缺失。其中卵巢浆液性囊腺癌、黏液性囊腺癌、内膜样腺癌患者组织中的p-mTOR蛋白阳性表达率依次为54.78%、58.33%、40.00%。卵巢上皮癌Ⅰ~Ⅱ期和Ⅲ~Ⅳ期患者中p-mTOR蛋白阳性表达率分别为23.05%和56.03%,Ⅲ~Ⅳ期患者明显高于Ⅰ~Ⅱ期(P<0.05)。在卵巢上皮癌高、中分化和低分化患者组织中,p-mTOR蛋白阳性表达率分别为53.95%和53.85%(P>0.05)。结论:p-mTOR在卵巢上皮癌中的高表达与肿瘤性质及发生发展相关,可能成为预测卵巢癌发生发展的新肿瘤标记物和治疗的靶点。 Objective:To investigate the expression of phosphorylate-mammalian target of rapamycin,p-mTOR,in epithelial ovarian cancer and its clinical significance.Methods:The expression of p-mTOR was detected individually in the specimens of 154 epithelial ovarian cancer,25 benign ovarian epithelia tumour,34 normal ovarian tissues by immunohistochemistry.The correlation of p-mTOR expression to clinicopathologic feature of epithelial ovarian cancer was analyzed.Results:The positive rate of p-mTOR in epithelial ovarian cancer was 53.90%.No expression was detected in benign ovarian epithelia tumour and normal ovarian tissues.The positive rate of p-mTOR in serous,mutinous,and endometriod ovarian adenocarcinoma was 54.78%,58.33%,and 40% respectively(P0.05).The positive rate of p-mTOR in Ⅰ/Ⅱ and Ⅲ/Ⅳ stage epithelial ovarian cancers tissues was 23.05% and 56.03% respectively(P0.05).The positive rate of p-mTOR was 53.95% and 53.85% respectively in high-moderately and poorly-differentiated epithelial ovarian cancers tissues(P0.05).Conclusion:The overexpression of p-mTOR is closely related to epithelial ovarian cancer initiation and progression.The p-mTOR may be served as a new tumor molecular marker and target for anticancer therapy.
出处 《中国妇幼保健》 CAS 北大核心 2012年第5期737-740,共4页 Maternal and Child Health Care of China
关键词 卵巢上皮癌 P-MTOR 免疫组织化学 Epithelial ovarian cancer P-mTOR Immunohistochemistry
  • 相关文献

参考文献11

  • 1Heintz AP, Odieino F, Maisonneuve Pet al. Carcinoma of the ovary [J] . Int J Gynaecol Obstet, 2003, 83 (Suppl 1) : 135.
  • 2Ahomare DA, Wang HQ, Skele KL et al. AKT and roTOR phosphorylation is frequently detected in ovarian cancer and can be targeted to disrupt ovarian tumor cell growth [J]. Oneogene, 2004, 23 (34) : 5853.
  • 3Camero A, Blanco - Aparicio C, Rennet O et al. The PTEN/PI3K/AKT signalling pathway in cancer, therapeutic implications [J].Curr Cancer Drug Targets, 2008, 8 (3) : 187.
  • 4Jiang BH, Liu LZ. PI3K/PTEN signaling in tumorigenesis and angiogenesis[J] . Biochim Biophys Acta, 2008, 1784 (1) : 150.
  • 5Campbell IG, Russell SE, Choong DY et al. Mutation of the PIK3CA gene in ovarian and breast cancer [J] . Cancer Res, 2004, 64 (21) : 7678.
  • 6Kolasa IK, Rembiszewska A, Janiec - Jankowska A et al. PTEN mutation, expression and LOH at its locus in ovarian carcinomas. Relation to TP53, K- ras and BRCA 1 mutations[J].Gyneeol Oneol, 2006, 103 (2) : 692.
  • 7Castellvi J, Garcia A, Rojo F et al. Phosphorylated 4E binding protein 1 : a halhnark of cell signaling that correlates with survival in ovarian cancer [J] . Cancer, 2006, 107 (8): 1801.
  • 8Mabuchi S, Altomare DA, Connolly DC et al. RAD001 (Everolimus) delays tumor onset and progression in a transgenic mouse model of ovarian cancer[J] . Cancer Res, 2007, 67 (6) : 2408.
  • 9Xu DZ, Geng QR, Tian Yet al. Activated mammalian target of rapamycin is a potential therapeutic target in gastric cancer [ J] . BMC Cancer,2010, 10:536.
  • 10Kruck S, Bedke J, Hennenlotter Jet al. Activation of mTOR in renal cell carcinoma is due to increased phosphorylation rather than protein overexpression [J] . Oneol Rep, 2010, 23 (1) : 159.

同被引文献26

  • 1刘奕,杨鸣良,张扬,于秉治.哺乳动物的雷帕霉素靶蛋白及其底物在口腔鳞状细胞癌中的表达[J].华西口腔医学杂志,2004,22(4):331-333. 被引量:8
  • 2Bradshaw SL, D'ercole AJ, Han VK. Overexpression of insu- lin-like growth factor - binding protein - 2 in C6 glioma cells results in conditional alteration of cellular growth [ J] . Endo- crinology, 1999, 140:575 -584.
  • 3Godard S, Getz G, Delorenzi M, et al. Classification of hu- man astroeyte gliomas on the basis of gene expression : a eorre-lated group of genes with angiogenic activity emerges as a strong predictor of subtypes [ J] . Cancer Res, 2003, 63: 6613 - 6625.
  • 4Wang GK, Hu L, Fuller GN, et al. An interaction between insulin - like growth factor - binding protein 2 ( IGFBP - 2 ) and integrin alpha 5 is essential for IGFBP - 2 - induced cell mobility [J] .J Biol Chem, 2006, 281:14085-14091.
  • 5Bensalah K, Lotan Y, Karam JA, et al. New circulating bio- markers for prostate cancer [ J ] . Prostate Cancer Prostatic Dis, 2008, 11: 112- 120.
  • 6Hua Wang, Huamin Wang, Weiping Shen. Insulin -like growth factor binding protein 2 enhances glioblastoma invasion by acti- vating invasion - enhancing genes [J] . Cancer Res, 2013, 63 : 4315 -4321.
  • 7Lee [J, Mircean C, Shmulevich I. Insulin -like growth factor binding protein 2 promotes ovarian cancer cell invasion [ J3 . MolCancel', 2005, 14 (1): 7.
  • 8VAN DER BILT AR, TERWISSCHA VAN SCHELTINGA AG,TIMMER-BOSSCHA H,et al. Measurement of tumor VEGF-Alevels with 89Zr-bevacizumab PET as an early biomarker for theantiangiogenic effect o. everolimus treatment in an ovarian cancerxenograft model[J]. Clin Cancer Res, 2012,18(22): 6306-6014.
  • 9HIRASAWA T, MIYAZAWA M, YASUDA M,et al. Alterationsof hypoxia-induced factor signaling pathway due to mammaliantarget of rapamycin (mTOR) suppression in ovarian clear celladenocarcinoma: in vivo and in vitro explorations for clinical trial[J]. Int J Gynecol Cancer, 2013,23(7): 1210-1218.
  • 10FENG X,LI L, JIANG H, et al. Dihydroartemisinin potentiatesthe anticancer effect of cisplatin via mTOR inhibition in cis-platin-resistant ovarian cancer cells: involvement of apoptosis andautophagy [J]. Biochem Biophys Res Commun, 2014,444 (3):376-381.

引证文献3

二级引证文献12

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