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宫颈癌细胞分泌外泌体介导上皮-间质转化提高癌前细胞侵袭能力的体外研究

易红艳 陈春林 钟梅 余艳红 周琛斐 梁莉 王薇 魏文斐 陈晓静 吴湘光 严瑞明 刘国炳

现代妇产科进展2017,Vol.26Issue(3):165-168,4.
现代妇产科进展2017,Vol.26Issue(3):165-168,4.DOI:10.13283/j.cnki.xdfckjz.2017.03.001

宫颈癌细胞分泌外泌体介导上皮-间质转化提高癌前细胞侵袭能力的体外研究

Exosomes derived from cervical carcinoma cells promote preneoplastic cell invasion in vitro via epithelial mesenchymal transition

易红艳 1陈春林 1钟梅 1余艳红 1周琛斐 1梁莉 2王薇 1魏文斐 1陈晓静 1吴湘光 1严瑞明 1刘国炳1

作者信息

  • 1. 南方医科大学南方医院 妇产科,广州 510515
  • 2. 南方医科大学南方医院 病理科,广州 510515
  • 折叠

摘要

Abstract

Objective:To investigate whether Exosomes secreted by cervical cancer cell lines Siha ( Siha-Exo) have ability to promote Ect1 invasion via epithelial mesenchymal transi-tion ( EMT) in cervical cancer. Methods:Morphology and marker protein of Siha-Exo isolated by different ultracentrifugation were identified by transmission electron microscopy and Western blot. And green fluorescent PKH67-labeled Siha-Exo detected by confocal images for biological activity. Ect1 was co-cultured with Siha-Exo or PBS for 48 hours. The expression of epithelial and mesenchyme markers were examined by Western blot. Transwell chambers were used in vitro invasion assay. Results:Siha-Exo exhibited typical cup-shaped vesicles and a size range of 30-100nm,expressed exosomal marker protein CD63 and CD81,and were biologically uptaked by recipient Ect1. Compared with PBS treated cells,Ect1 treated with Siha-Exo decreased ex-pression of epithelial marker E-Cadherin andβ-Catenin,and increased expression of mesenchy-mal marker N-Cadherin and Vimentin. Meanwhile in Siha-Exo group,numbers of Ect1 penetrat-ing transwell membrane significantly increased in contrast with PBS group ( P=0 . 01 ) . Conclu-sion:Siha-Exo elicited Ect1 to an EMT-like phenotype,thus promoting invasion in vitro.

关键词

外泌体/宫颈癌/上皮间质转化/侵袭

Key words

Exosomes/Cervical cancer/Epithelial mesenchymal transition/Invasion

分类

医药卫生

引用本文复制引用

易红艳,陈春林,钟梅,余艳红,周琛斐,梁莉,王薇,魏文斐,陈晓静,吴湘光,严瑞明,刘国炳..宫颈癌细胞分泌外泌体介导上皮-间质转化提高癌前细胞侵袭能力的体外研究[J].现代妇产科进展,2017,26(3):165-168,4.

基金项目

国家自然科学基金(No:81072132 ()

81372871 ()

81672589 ()

JCYJ20160429161218745) ()

现代妇产科进展

OA北大核心CSCDCSTPCD

1004-7379

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