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[1]陈 慧,张 兰,郭以河,等.Eag1钾离子通道在卵巢癌组织中的表达及意义[J].医学研究与战创伤救治(原医学研究生学报),2016,18(01):17-20.[doi:10.3969/j.issn.1672-271X.2016.01.005]
 CHEN Hui,ZHANG Lan,GUO Yi-he,et al.Expression and significance ofether à go-go 1 channels in human ovarian cancer[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2016,18(01):17-20.[doi:10.3969/j.issn.1672-271X.2016.01.005]
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Eag1钾离子通道在卵巢癌组织中的表达及意义()

《医学研究与战创伤救治》(原医学研究生学报)[ISSN:1672-271X/CN:32-1713/R]

卷:
第18卷
期数:
2016年01期
页码:
17-20
栏目:
出版日期:
2016-01-20

文章信息/Info

Title:
Expression and significance ofether à go-go 1 channels in human ovarian cancer
作者:
陈 慧1张 兰1郭以河2林月丽1洪丽玲1
363000 福建漳州,厦门大学附属东南医院,1.妇产科,
2.病理科
Author(s):
CHEN Hui1 ZHANG Lan1 GUO Yi-he2 LIN Yue-li1 HONG Li-lin1.
1. Department of Gynaecology and Obstetrics,
2. Department of Pathology, the Affiliated Southeast Hospital of Xiamen University, Zhangzhou, Fujian 363000, China
关键词:
Eag1阿司咪唑增殖免疫组织化学卵巢癌
Keywords:
human ether à go-go1 astemizole proliferation cell cycle immunohistochemistry ovarian cancer
分类号:
R737.31
DOI:
10.3969/j.issn.1672-271X.2016.01.005
文献标志码:
A
摘要:
目的 检测Ether à go-go 1(Eag1) 钾离子通道在人卵巢癌中的表达,对人卵巢癌细胞株SKOV3的影响及与卵巢癌患者临床特征的关系。方法 用实时定量逆转录- 聚合酶链反应 (qRT-PCR) 检测卵巢癌细胞SKOV3中Eag1的表达;用噻唑蓝比色法 (MTT) 检测Eag1钾离子通道抑制剂阿司咪唑 (Astemizole) 对SKOV3细胞增殖的影响;用流式细胞 仪检测阿司咪唑对对SKOV3细周期的影响;用蛋白印迹法 (Western blot) 和免疫组织化学的方法检测36例卵巢癌组织中Eag1蛋白的表达并结合临床病例资料进行分析。结果 阿司 咪唑可明显抑制SKOV3细胞增殖,阻滞细胞周期于G0/G1期。在卵巢癌标本中,Eag1蛋白的阳性表达率明显高于正常卵巢组织。其在不同的临床分期方面差异有统计学意义(P<0.05) 。结论 Eag1钾离子通道异常表达于人卵巢癌组织中,并可能成为卵巢癌诊断和治疗的靶点。
Abstract:
Objective To evaluate the expression of Eag1 potassium channel in human ovarian cancer, the effects of Eag1 on human ovarian cancer cell line SKOV3 and the relationship between Eag1 expression and clinicopathological characteristics of ovarian cancer patients. Methods The expression of Eag1 in human ovarian cancer cell line SKOV3 was detected by quantificational reverse transcription polymerase chain reaction (qRT-PCR). The effects of astemizole (a inhibitor of Eag1) on SKOV3 cells proliferation and cycle were measured by MTT and ow cytometry. Then the expressions of Eag1 at protein level were detected by Western blot and immunohistochemical staining in 36 cases of ovarian cancer. The relationship between the index and clinicopathological parameters was analyzed. Results Eag1 was overexpressed in SKOV3 cells. Cell proliferation and cycle can be significantly inhibited by astemizole. Eag1 was expressed higher in the ovarian cancer specimens than in normal ovaries tissues and was associated with clinical stage (P<0.05). Conclusion The expression of Eag1 potassium channel was aberrant in human ovarian cancer tissues and Eag1 potassium channel may represent a potential target for ovarian cancer diagnosis and treatment.

参考文献/References:

[1]朱饮源,姚 军,李 曼. 糖原合成酶激酶3β对卵巢癌紫杉醇耐药性的影响及机制研究[J]. 东南国防医药,2015, 17(1):29-31.
[2]曹王丽,宋佳希,李芳秋. 单克隆抗体靶向治疗卵巢癌研究进展[J]. 医学研究生学报, 2013, 26(5):536-540.
[3]Ozakpinar OB, Maurer AM, Ozsavci D. Ovarian stem cells: from basic to clinical applications[J]. World J Stem Cells,2015, 26, 7(4):757-768.
[4]Warmke JW, Ganetzky B. A family of potassium channel genes related to eag in drosophila and mammals[J]. Proc Natl Acad Sci USA, 1994, 91(8): 3438-3442.
[5]Camacho J. Ether à go-go potassium channels and cancer[J]. Cancer Lett, 2006, 233(1):1-9.
[6]刘黎琼, 李慧玉, 黄士昂. herg1基因与肿瘤[J]. 国际病理科学与临床杂志, 2006, 27(1): 15-18.
[7]翁占平, 王 波. TASK23钾离子通道的研究现状[J]. 国际病理科学与临床杂志, 2006, 26(3): 225-231.
[8]Farias LM, Ocaa DB, Díaz L, et al. Ether à go-go potassium channels as human cervical cancer markers[J]. Cancer Res, 2004, 64(19): 6996-7001.
[9]Ding XW, Wang XG, Luo HS, et al. Expression and prognostic roles of Eag1 in resected esophageal squamous cell carcinomas[J]. Dig Dis Sci, 2008, 53 (8):2039-2044.
[10]Ding XW, Yan JJ, An P, et al. Aberrant expression of ether a go-go potassium channel in colorectal cancer patients and cell lines[J]. World J Gastroenterol, 2007, 13(8): 1257-1261.
[11]Ding XW, Luo HS, Jin X, et al. Aberrant expression of EAG1 potassium channel in gastric cancer patients and cell lines[J]. Med Oncol, 2007, 24(3): 345- 350.
[12]Pardo LA, Del Camino D, Sanchez A, et al. Oncogenic potential of EAG K+ channels[J]. EMBO J, 1999, 18(20): 5540-5547.
[13]Occhiodoro T, Bernherim L, Liu JH, et al. Cloning of a human ether-a-go-go potassium channel expressed in myoblasts at the onset of fusion[J]. FEBS Lett, 1998, 434(1-2): 177-182.
[14]Hemmerlein B, Weseloh RM, De Queiroz FM, et al. Overexpression of EAG1 potassium channels in clinical tumours[J]. Mol Cancer, 2006,41(5):1-13.
[15]Mello de Queiroz F, Suarez-Kurtz G, Stühmer W, et al. Ether à go-go potassium channel expression in soft tissue sarcoma patients[J]. Mol Cancer, 2006, 42(5): 1-10.
[16]Agarwal JR, Griesinger F, Stühmer W, et al. The potassium channel ether à go-go is a novel prognostic factor with functional relevance in acute myeloid leukemia[J]. Mol Cancer, 2010, 9(18): 2-16.
[17]Asher V, Khan R, Warren A, et al. The Eag potassium channel as a new prognostic marker in ovarian cancer[J]. Diagn Pathol, 2010, 5:78.
[18]Borowiec AS, Hague F, Harir N, et al. IGF-1 activates hEAG K+ channels through an Akt-dependent signaling pathway in breast cancer cells: role in cell proliferation[J]. J Cell Physiol, 2007, 212(3): 690-701.
[19]Ortia CS, Montante-Montes D, Saqui-Salces M, et al. EAG1 potassium channels as markers of cervical dysplasia[J]. Oncol Rep, 2011, 26(6): 1377-1383..
[20]Diaz L, Ceja-Ochoa I, Restrepo-Angulo I, et al. Estrogens and human papilloma virus oncogenes regulate human ether-a-go-go-1 potassium channel expressed [J]. Cancer Res, 2009, 69(8): 3300-3307.
[21]Restrepo-Angulo I, Sánchez-Torres C, Camacho J. Human EAG1 potassium channels in the epithelial-to-mesenchymal transition in lung cancer cells[J]. Anti Cancer Res, 2011, 31(4): 1265-1270.
[22]Downie BR, Sánchez A, Kntgen H, et al. Eag1 expression interferes with hypoxia homeostasis and induces angiogenesis in tumors[J]. J Biol Chem, 2008, 283(52): 36234-36240.
[23]Sahoo N, Trger J, Heinemann SH, et al. Current inhibition of human EAG1 potassium channels by the Ca2+ binding protein S100B[J]. FEBS Letters, 2010, 584(18): 3896-3900.
[24]Sorci G, Riuzzi F, Arcuri C, et al. S100B protein in tissue development, repair and regeneration[J]. World J Biol Chem, 2013, 4(1): 1-12.

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备注/Memo

备注/Memo:
福建省漳州市自然科学计划项目(ZZ2012J25)
更新日期/Last Update: 2016-01-20