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腺苷酸活化蛋白激酶在卵巢肿瘤中的表达及临床意义

Expression and significance of AMP-activated protein kinase in ovarian tumor
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摘要 目的探讨腺苷酸活化蛋白激酶(AMPK)在卵巢肿瘤组织中的表达及临床意义。方法收集手术标本存档蜡块56份。其中,正常卵巢组织6份,卵巢良性上皮性肿瘤组织20份,卵巢癌组织30份。用免疫组化比较各组蜡块标本AMPKα1、AMPKα2及p-AMPK蛋白表达。结果AMPKα1蛋白表达于细胞的胞浆;卵巢癌组织中AMPKα1蛋白的阳性表达率为30%,与卵巢良性肿瘤组织的35%和正常卵巢组织的33%相仿(P>0.05)。AMPKα2蛋白也表达于胞浆,少量表达于胞核;其在卵巢癌中的阳性表达率为80%,明显高于卵巢良性肿瘤组织的45%和正常卵巢组织的33%(P<0.05)。卵巢癌中p-AMPK蛋白表达明显低于卵巢良性肿瘤组织和正常卵巢组织(P<0.05)。AMPKα1和AMPKα2蛋白的表达与不同临床病理指标之间无明显相关性。结论卵巢癌组织中AMPKα2蛋白高表达,表明AMPK信号传导途径在卵巢癌发病机制中有重要作用。 Objective To investigate the expression and significance of AMP-activated protein kinase in ovarian tumors. Methods Immunohistochemical staining was used to examine the expressions of AMPKal, AMPKa2 and p-AMPK in 30 patients with ovarian carcinoma(group A), 20 cases with ovarian cystadenoma (group B) and 6 normal ovarian tissue samples (group C). Results The AMPKal and AMPKa2 were expressed in the cytoplasm and AN/PKa2 was expressed in the nucleus in a small amount as well. The positive expression rate of AMPKal protein in group A was 30% ,which was similar to 35% in group B and 33% in group C(P〉0. 05). The positive expression rate of AMPKa2 protein in group A was 80%, which was significantly higher than 45% in group B and 33% in group C(P〈0. 05). The positive expression of p-AMPK in group A was lower than that in groups of B and C (P〈0. 05). The positive expressions of AMPKal and AMPKa2 were not correlated to the clinicopathological parameters. Condution AMPKa2 is overexpressed in ovarian cancer, suggesting that AMPK signal pathway plays an important role in the development of ovarian cancer.
出处 《江苏医药》 CAS 北大核心 2013年第16期1895-1897,F0003,共4页 Jiangsu Medical Journal
关键词 腺苷酸活化蛋白激酶 卵巢肿瘤 AMP-activated protein kinase Ovarian tumor
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参考文献8

  • 1Chen MB, Shen WX, Yang Y, et al. Activation of AMP- activated protein kinase is involved in vincristine-induced cell apoptosis in B16 melanoma cell[J]. J Cell Physiol, 2011,226 (7) : 1915-1925.
  • 2Chen MB,Wu XY, Tao GQ, et al. Perifosine sensitizes curcu- min-induced anti-colorectal cancer effects by targeting multiple signaling pathways both in vivo and in vitro[J]. Int J Cancer, 2012,131(11) : 2487-2498.
  • 3Sun H,Yu T, Li J. Co-administration of perifosine with pacli- taxel synergistically induces apoptosis in ovarian cancer cells: more than just AKT inhibition[J]. Cancer Lett, 2011,310 ( 1 ) : 118-128.
  • 4Pan W, Yang H, Cao C, et al. AMPK mediates curcumin- induced cell death in CaOV3 ovarian cancer cells[J]. Oncol Rep, 2008,20 (6) : 1553-1559.
  • 5徐春琳,路晓琳,闫晓楠,王惠兰,陈素琴.PI3K/Akt/NF-κB信号通路在FSH促进卵巢癌细胞增殖与侵袭中的作用[J].中华妇产科杂志,2012,47(2):134-138. 被引量:10
  • 6Cuthbertson DJ, Babraj JA, Mustard KJ, et al. 5 aminoimid- azole-4-carboxamide 1-beta-D-ribofuranoside acutely stimulates skeletal muscle 2 deoxyglucose uptake in healthy men[J]. Diabetes, 2007,56 (8) .- 2078-2084.
  • 7Zhang HY,Zhang PN,Sun H. Aberration of the PI3K/AKT/ roTOR signaling in epithelial ovarian cancer and its implication in cisplatin-based chemotherapy [ J ]. Eur J Obstet Gynecol Reprod Biol, 2009,146 (1) : 81-86.
  • 8Li C, Liu VW, Chiu PM, et al. Over-expressions of AMPK subunits in ovarian carcinomas with significant clinical implications[J]. BMC Cancer,2012,12(1):357.

二级参考文献16

  • 1Choi JH, Wong AS, Huang HF, et al. Gonadotropins and ovarian cancer. Endocr Rev ,2007 ,28 :440-461.
  • 2McSorley MA, Alberg AJ, Allen DS, et al. Prediagnostic circulating follicle stimulating hormone concentrations and ovarian cancer risk. Int J Cancer,2009,125:674-679.
  • 3Ji Q, Liu PI, Chen PK, et al. Follicle stimulating hormone- induced growth promotion and gene expression profiles on ovarian surface epithelial ceils. Int J Cancer,2004,112:803-814.
  • 4Park YH, Kim SJ, Jeong BH, et al. Follicular stimulating hormone enhances Notch 1 expression in SK-OV-3 ovarian cancer ceils. J Gynecol 0ncol,2010,21:119-124.
  • 5Arslan AA, Zeleniuch-Jacquotte A, Lundin E, et al. Serum follicle-stimulating hormone and risk of epithelial ovarian cancer in postmenopausal women. Cancer Epidemiol Biomarkers Prey, 2003,12:1531-1535.
  • 6Ohtani K, Sakamoto H, Kikuehi A, et al. Follicle-stimulating hormone promotes the growth of human epithelial ovarian cancer ceils through the protein kinase C-mediated system. Cancer Lett, 2001,166:207-213.
  • 7Carvalho CR, Carvalheira JB, Lima MH, et al. Novel signal transduction pathway for luteinizing hormone and its interaction with insulin: activation of Janus kinase/signal transducer and activator of transcription and phosphoinositol 3-kinase/Akt pathways. Endocrinology,2003,144:638-647.
  • 8Meronl SB, Riera ME, Pelllzzan EH, et al. FSH activates phosphatidylinositol 3-kinase/protein kinase B signaling pathway in 20-day-old Sertoli cells independently of IGF-I. J Endoerinol, 2004,180:257-265.
  • 9Bader AG, Kang S, Zhao L, et al. Oncogenic PI3K deregulates transcription and translation. Nat Rev Cancer,2005,5:9")1-929.
  • 10Engelman JA, Luo J, Cantley LC. The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism. Nat Rev Genet,2006,7:606--619.

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