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尼古丁诱导肺癌细胞上皮间质转化促进其侵袭转移

侯艳须 沈旺 周清华 李雪冰 潘振华 祖玲玲 范亚光 尤嘉琮 王玉丽 王岷 陈沛锐

中国肺癌杂志2016,Vol.19Issue(4):169-176,8.
中国肺癌杂志2016,Vol.19Issue(4):169-176,8.DOI:10.3779/j.issn.1009-3419.2016.04.11

尼古丁诱导肺癌细胞上皮间质转化促进其侵袭转移

Nicotine Induced Lung Cancer Cells Epithelial-mesenchymal Transition and Promote Its Vitro Invasion Potential

侯艳须 1沈旺 1周清华 1李雪冰 2潘振华 1祖玲玲 1范亚光 1尤嘉琮 1王玉丽 1王岷 1陈沛锐1

作者信息

  • 1. 300052天津,天津市肺癌转移与肿瘤微环境重点实验室,天津市肺癌研究所,天津医科大学总医院
  • 2. 610041成都,四川大学华西医院肺癌中心
  • 折叠

摘要

Abstract

Background and objective Our previous study found that nicotine could induce lung cancer cell epithelial-mesenchymal transition (EMT). The aim of this study is to explore the relationship between nicotine-induced EMT and lung cancer invasion and metastasis. Methods Real-time PCR and Western blot were used to detect the expression changes of EMT-related markers, E-cadherin and Vimentin, in A549 lung cancer cells treated with nicotine;hTe transposition ofβ-catenin protein expression was determined by immunolfuorescence;Scratch test and Transwell invasion assay were used to detect the effects of nicotine on lung cancer cell migration and invasion. Results Nicotine can signiifcantly down-regulate the expressional level of E-cadherin mRNA and protein of A549 cells in a manner of dose and time-dependent (P<0.01, P<0.01);Nicotine can signiifcantly up-regulate the expressional level of Vimentin mRNA and protein of A549 cells in a manner of dose and time-dependent (P<0.01, P<0.01);Immunolfuorescence results showed thatβ-catenin protein was signiifcantly transfered to nucleus;Scratch test and Transwell assay showed that Nicotine could remarkably increase the migration and invasion poten-tial of lung cancer cells (P<0.01, P<0.01). Conclusion Nicotine can induce cancer cells EMT, and promote the invasion and metastasis ability of lung cancer cells.

关键词

肺肿瘤/尼古丁/上皮间质转化/侵袭

Key words

Lung neoplasms/Nicotine/Epithelial-mesenchymal transition/Invasion

引用本文复制引用

侯艳须,沈旺,周清华,李雪冰,潘振华,祖玲玲,范亚光,尤嘉琮,王玉丽,王岷,陈沛锐..尼古丁诱导肺癌细胞上皮间质转化促进其侵袭转移[J].中国肺癌杂志,2016,19(4):169-176,8.

基金项目

本研究受国家自然科学基金(No.81572288)和教育部高等学校博士点优先发展领域基金(No.20131202130001)资助 ()

中国肺癌杂志

OA北大核心CSCDCSTPCDMEDLINE

1009-3419

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