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非小细胞肺癌组织中MAGE-A3和MAGE-C2 mRNA的表达

马星 陈新峰 张超奇 乔亚敏 张毅 王丽萍

郑州大学学报(医学版)2017,Vol.52Issue(5):580-585,6.
郑州大学学报(医学版)2017,Vol.52Issue(5):580-585,6.DOI:10.13705/j.issn.1671-6825.2017.05.016

非小细胞肺癌组织中MAGE-A3和MAGE-C2 mRNA的表达

Expressions of MAGE-A3 and MAGE-C2 mRNA in non-small cell lung carcinoma tissue

马星 1陈新峰 2张超奇 2乔亚敏 2张毅 1王丽萍2

作者信息

  • 1. 郑州大学第一附属医院肿瘤科 郑州450052
  • 2. 郑州大学第一附属医院生物细胞治疗中心 郑州450052
  • 折叠

摘要

Abstract

Aim:To analyze the expressions of MAGE-A3 and MAGE-C2 mRNA in non-small cell lung cancer (NSCLC) tissue and the relationship between their expressions and clinical pathological characteristics .Methods:Tumor tissue was collected from 206 patients diagnozed as NSCLC .Real-time PCR was performed to detect the expressions of MAGE-A3 and MAGE-C2 mRNA.The correlation of clinicopathological characteristics (gender, age, histologic grading, pathological type , lymph node metastasis , clinical stage ) with the expressions of MAGE-A3 and MAGE-C2 mRNA in NSCLC tissue was evaluated .Then siRNA was used to down-regulate the expression of MAGE-A3 in A549 cells and the effects of MAGE-A3 knockdown on biology behavior of A 549 cells were observed .Results:The mRNA expression rates of MAGE-A3 and MAGE-C2 in NSCLC tissue were 73.3%(151/206) and 52.9%(109/206), respectively.The mRNA ex-pression of MAGE-A3 was associated with clinical stage and lymph node metastasis (P<0.05).However, there was no re-lation between MAGE-C2 mRNA expression and clinical characteristics (P>0.05).The mRNA coexpression of MAGE-A3 and MAGE-C2 was associated with age and clinical stage (P<0.05).MAGE-A3 knockdown led to decrease of sphere for-mation, invasion, and metastasis abilities of cells(P<0.001).Conclusion: MAGE-A3 and MAGE-C2 are expressed in NSCLC at high level;MAGE-A3 and MAGE-C2 might be potential target antigens for immunotherapy of NSCLC .

关键词

非小细胞肺癌/MAGE-A3/MAGE-C2

Key words

non-small cell lung cancer/MAGE-A3/MAGE-C2

分类

医药卫生

引用本文复制引用

马星,陈新峰,张超奇,乔亚敏,张毅,王丽萍..非小细胞肺癌组织中MAGE-A3和MAGE-C2 mRNA的表达[J].郑州大学学报(医学版),2017,52(5):580-585,6.

基金项目

国家自然科学基金资助项目 81171986,81271815 ()

科技部国家重点研发计划 2016YFC1303500 ()

郑州大学学报(医学版)

OA北大核心CSTPCD

1671-6825

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