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ANXA2对Caco2细胞凋亡的影响 被引量:2

The effect of ANXA2 expression on the apoptosis of Caco2 cells
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摘要 为研究膜联蛋白A2(ANXA2)基因与人结直肠癌Caco2细胞凋亡之间的关系,采用RNAi技术沉默Caco2细胞的ANXA2表达后,利用流式细胞仪分析细胞凋亡水平,并利用激光共聚焦显微镜和透射电子显微镜对凋亡细胞进行形态学检测。流式细胞仪检测结果显示,ANXA2表达被抑制后细胞线粒体正常膜电位发生改变(P<0.05),线粒体结构受损;同时,形态学检测结果表明,ANXA2表达被抑制后细胞出现了较为明显的凋亡样特征。结果提示:ANXA2在人结直肠癌Caco2细胞的高表达能一定程度地促进细胞生长,抑制ANXA2表达可以诱导细胞出现一定程度的凋亡样形态特征,但不足以引起细胞广泛而明显的凋亡;推测ANXA2表达水平并不是唯一影响瘤细胞凋亡的因素。该结果支持关于ANXA2具有作为肿瘤靶向诊断、治疗靶分子潜能的推论。 To study the relationship between ANXA2 and the apoptosis of Caco2 cells,the expression of ANXA2 in Caco2cells was inhibited by siRNA.Cell apoptosis was further investigated by flow cytometry(FCM),and morphological characteristics were observed with laser scanning confocal microscopy(CLSM)and transmission electron microscopy(TEM).The results showed that the fluorescence density of the cells was significantly reduced in ANXA2 interfered groups(P<0.05),suggesting that the normal membrane potential of mitochondria has been changed.Moreover,some characteristics of apoptosis cells were also observed in ANXA2 silenced cells compared to control group.Taken together,these results indicate that the excessive expression of ANXA2 in Caco2cells could promote the proliferation of Caco2 cells.Moreover,some morphological characteristics of apoptosis may be induced by silencing ANXA2 in Caco2cells,but it is insufficient to cause widely apoptosis or obvious characteristics of cell apoptosis.We suppose that the excessive expression of ANXA2 is not unique route of anti-apoptosis factors of tumor.These results further confirm that ANXA2 has great potential as a targeting molecule of tumor diagnosis and treatment.
出处 《陕西师范大学学报(自然科学版)》 CAS CSCD 北大核心 2015年第1期75-79,共5页 Journal of Shaanxi Normal University:Natural Science Edition
基金 陕西省自然科学基金资助项目(SF2009178)
关键词 膜联蛋白A2 结直肠癌细胞 细胞凋亡 基因表达 基因功能 ANXA2 colorectal carcinoma cells cell apoptosis gene expression gene function
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  • 1Cindy Gallerne,Alexandre Prola,Christophe Lemaire.Hsp90 inhibition by PU-H71 induces apoptosis through endoplasmic reticulum stress and mitochondrial pathway in cancer cells and overcomes the resistance conferred by Bcl-2[J]. BBA - Molecular Cell Research . 2013 (6) 被引量:1
  • 2Xiaohui Zhang,Shuqing Liu,Chunmei Guo,Junwei Zong,Ming-Zhong Sun.The association of annexin A2 and cancers[J]. Clinical and Translational Oncology . 2012 (9) 被引量:2
  • 3Thomas Grewal,Carlos Enrich.Annexins — Modulators of EGF receptor signalling and trafficking[J]. Cellular Signalling . 2009 (6) 被引量:1
  • 4Hongyu Bao,Miao Jiang,Mingqing Zhu,Fei Sheng,Jia Ruan,Changgeng Ruan.Overexpression of Annexin II affects the proliferation, apoptosis, invasion and production of proangiogenic factors in multiple myeloma[J]. International Journal of Hematology . 2009 (2) 被引量:1
  • 5Gourab Bhattacharjee,Jasimuddin Ahamed,Rafal Pawlinski,Cheng Liu,Nigel Mackman,Wolfram Ruf,Thomas S. Edgington.Factor Xa Binding to Annexin 2 Mediates Signal Transduction via Protease-Activated Receptor 1[J]. Circulation Research . 2008 (4) 被引量:1
  • 6Yun Huang,Yan Jin,Cheng-hui Yan,Yang Yu,Jing Bai,Feng Chen,Yu-zhen Zhao,Song-bin Fu.Involvement of Annexin A2 in p53 induced apoptosis in lung cancer[J]. Molecular and Cellular Biochemistry . 2008 (1) 被引量:2
  • 7Elena Ortiz-Zapater,Sandra Peiró,Oriol Roda,Josep M. Corominas,Susana Aguilar,Coral Ampurdanés,Francisco X. Real,Pilar Navarro.Tissue Plasminogen Activator Induces Pancreatic Cancer Cell Proliferation by a Non-Catalytic Mechanism That Requires Extracellular Signal-Regulated Kinase 1/2 Activation through Epidermal Growth Factor Receptor and Annexin A2[J]. The American Journal of Pathology . 2007 (5) 被引量:1
  • 8Jianxin Mai,David M. Waisman,Bonnie F. Sloane.Cell surface complex of cathepsin B/annexin II tetramer in malignant progression[J]. Biochimica et Biophysica Acta (BBA)/Protein Structure and Molecular Enzymology . 2000 (1) 被引量:1
  • 9Yangping Chiang,Angie Rizzino,Zita A. Sibenaller,Marc S. Wold,Jamboor K. Vishwanatha.Specific down-regulation of annexin II expression in human cells interferes with cell proliferation[J]. Molecular and Cellular Biochemistry . 1999 (1) 被引量:1
  • 10Rescher U,Gerke V.Annexins-unique membrane binding proteins with diverse functions. Journal of Cell Science . 2004 被引量:2

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  • 1Chen CY, Lin YS, Chen CL, et al. Targeting annexin A2 reducestumorigenesis and therapeutic resistance of nasopharyngeal carcino-ma[ J]. Oncotarget,2015 , 6(29) :26946 - 26959. 被引量:1
  • 2Choi DS, Yang JS, Choi EJ, et al. The protein interaction net-work of extracellular vesicles derived from human colorectal cancer. 被引量:1
  • 3谢蕊,李燕京,隋红,等.ANXA2调节胃癌细胞的增殖、侵袭和转移[J].临床与病理杂志,2015,35(21):S78-S79. 被引量:1
  • 4Tristante E,Martinez CM,Jim6nez S,et al. Association of acharacteristic membrane pattern of annexin A2 with high invasive-ness and nodal status in colon adenocarcinoma [ J ]. Transl Res,2015,166(2):196-206. 被引量:1
  • 5Gurluier E, Guner OS, Tumay LV, et al. Serum annexin A2 lev-els in patients with colon cancer in comparison to healthy controlsand in relation to tumor pathology [ J ]. Med Sci Monit, 2014,3(20) :1801 -1807. 被引量:1
  • 6Tsukamoto H, Tanida S, Ozeki K, et al. Annexin A2 regulates adisintegrin and metalloproteinase 17-mediated ectodomain sheddingof pro-tumor necrosis factor-a in monocytes and colon epithelialcells [J]. Inflamm Bowel Dis, 2013,19(7) : 1365 ~ 1373. 被引量:1
  • 7Elena Tristantea, Carlos M. Martlnezb, Sofia Jim6nezc, et al. As-sociation of a characteristic membrane pattern of annexin A2 withhigh invasiveness and nodal status in colon adenocarcinoma[ J].Translational Research, 2015 , 166(2):196-206. 被引量:1
  • 8Qi Zhang, Zhongsheng Zhao, Yingyu Ma, et al. Combined ex-pression of S100A4 and Annexin A2 predicts disease progressionand overall survival in patients with urothelial carcinoma[ J]. Uro-logic Oncology, 2014,32(6) :798 -805. 被引量:1
  • 9秦呈林,查文章,姚登福,张海健.膜联蛋白A2异常表达与消化道肿瘤发生、发展的关系[J].中华临床医师杂志(电子版),2012,6(4):103-106. 被引量:4
  • 10刘向强,张志勇,孙力.MicroRNA-499-5p通过靶向FOX04和PDCD4促进大肠癌细胞侵袭和肿瘤转移[J].医学争鸣,2012(4):3-3. 被引量:1

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