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二甲双胍对甲状腺未分化癌侵袭转移的影响及机制研究

张丽娟 郏文亭 兰玲 钱玮 杨雪阳 徐宽枫 崔岱

南京医科大学学报(自然科学版)2017,Vol.37Issue(5):554-558,5.
南京医科大学学报(自然科学版)2017,Vol.37Issue(5):554-558,5.DOI:10.7655/NYDXBNS20170507

二甲双胍对甲状腺未分化癌侵袭转移的影响及机制研究

The study on the effect of metformin on invasion and metastasis of undifferentiated thyroid cancer and its underlying mechanisms

张丽娟 1郏文亭 1兰玲 2钱玮 3杨雪阳 1徐宽枫 1崔岱1

作者信息

  • 1. 南京医科大学第一附属医院内分泌科,江苏南京210029
  • 2. 江苏省老年医院内科,江苏南京210024
  • 3. 北京积水潭医院内分泌科,北京 100035
  • 折叠

摘要

Abstract

Objective:To observe the effects of mefformin on the invasion and metastasis of undifferentiated thyroid cancer and to evaluate its underlying mechanisms.Methods:The undifferentiated thyroid cancer cell line SW1736 was treated with different concentrations of mefformin.The invasive and metastatic abilities of SW1736 cells were measured by agar drop method and Transwell invasion and migration assay.Real-time PCR was used to detect the molecules mRNA involved in the process of epithelial-mesenchymal transition (EMT),including vimentin,E-cadherin and transcription factors Snail1 and Slug.Results:Metformin inhibited the invasive and migration capacities of SW1736 cells in vitro.The inhibitory effects of metformin were dose dependent.Mefformin significantly down-regulated the expressions of vimentin,Slug and Snail 1 in SW1736 cells.Meanwhile,it stimulated the expression of E-cadherin,which highly expresses in epithelial cells.Conclusion:Metformin can promote the expression of E-cadherin by down-regulating the expression of Snail1 and Slug,thus inhibiting the process of EMT and decreasing the invasive and migration ability of thyroid carcinoma,which may provide a novel strategy for the treatment of thyroid neoplasms.

关键词

二甲双胍/甲状腺未分化癌/侵袭/转移/上皮间质转化

Key words

metformin/undifferentiated thyroid cancer/invasion/metastasis/epithelial-mesenchymal transition

分类

医药卫生

引用本文复制引用

张丽娟,郏文亭,兰玲,钱玮,杨雪阳,徐宽枫,崔岱..二甲双胍对甲状腺未分化癌侵袭转移的影响及机制研究[J].南京医科大学学报(自然科学版),2017,37(5):554-558,5.

基金项目

江苏省“六大人才高峰”高层次人才项目(WSN-023) (WSN-023)

南京医科大学学报(自然科学版)

OA北大核心CSCDCSTPCD

1007-4368

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