Expression pattern of estrogen receptor β and its correlation with multidrug resistance in non-small cell lung cancer

被引:7
作者
Huang, L. [1 ,2 ]
Liu, T. [3 ]
Ji, H. [1 ,2 ]
Yang, S. [3 ]
Sui, J. [3 ]
Yang, W. S. [4 ,5 ]
Liang, G. Y. [3 ]
Zhang, X. M. [2 ,6 ]
机构
[1] Nanjing Med Univ, Jiangsu Canc Hosp, Dept Radiat Oncol, Affiliated Canc Hosp, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Jiangsu Inst Canc Res, Affiliated Canc Hosp, Nanjing, Jiangsu, Peoples R China
[3] Southeast Univ, Key Lab Environm Med Engn, Minist Educ, Sch Publ Hlth, Nanjing, Jiangsu, Peoples R China
[4] Zhejiang Univ, Dept Epidemiol, Sch Publ Hlth, Hangzhou, Zhejiang, Peoples R China
[5] Sch Basic Med Sci, Dept Social Sci & Publ Hlth, Jiujiang, Jiangxi, Peoples R China
[6] Nanjing Med Univ, Affiliated Canc Hosp, Dept Genet & Mol Biol, Jiangsu Canc Hosp, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
lung cancer; estrogen receptor beta; MDR1; P-glycoprotein; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER; P-GLYCOPROTEIN; ER-BETA; PACLITAXEL-RESISTANCE; SURVIVAL DIFFERENCES; DRUG-RESISTANCE; PROTEIN; ALPHA; REVERSAL;
D O I
10.4149/neo_2018_181120N872
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of this work was to determine the expression of the ER beta (estrogen receptor beta) and multidrug resistance, namely MDR1 (P-glycoprotein, P-gp), in 152 samples of non-small cell lung cancer. The expression pattern of ER beta and MDR1 were assessed by the quantitative reverse-transcriptase polymerase chain reaction (qRT-PCR) and immunohistochemistry. We also analyzed the correlation between ER beta and MDR1 with clinical and pathological data. The co-expression pattern of ER beta and individual MDR1 proteins was assessed by correspondence analysis and chi-squared tests. In the present study, we found that patients with tumor stage I-II showed higher ER beta mRNA expression levels and decreased expression of ER beta protein with increasing tumor grade, which is opposite to MDR1 expression. In addition, an opposite co-expression pattern of ER beta and individual MDR1 proteins was also observed. In conclusion, the results can be used to better understand the expression control of MDR1 and may allow for the establishment of new cancer chemistry strategies that will control P-gp expression in NSCLC.
引用
收藏
页码:847 / 857
页数:11
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