Literature DB >> 23803067

mRNA expression and clinical significance of ERCC1, BRCA1, RRM1, TYMS and TUBB3 in postoperative patients with non-small cell lung cancer.

Yi Han1, Xiao-Bin Wang, Ning Xiao, Zhi-Dong Liu.   

Abstract

BACKGROUND: To explore mRNA expression and clinical significance of ERCC1, BRCA1, RRM1, TYMS and TUBB3 genes in tumor tissue of postoperative patients with non-small cell lung cancer (NSCLC).
MATERIALS AND METHODS: Sixty NSCLC patients undergoing radical operation in our hospital from Nov., 2011 to Jun., 2012 were selected. Plasmid standards of ERCC1, BRCA1, RRM1, TYMS and TUBB3 were established and standard curves were prepared by SYBR fluorescent real-time quantitative PCR analysis. Samples from tumor centers were taken to detect mRNA expression of ERCC1, BRCA1, RRM1, TYMS and TUBB3 genes in cancerous tissue during operation. The total mRNA expression quantities were compared according to different clinical characteristics.
RESULTS: The total expression quantities of 5 genotypes from high to low were ERCC1>RRM1>TUBB3>TYMS>BRCA1 in turn. By pairwise comparisons, other differences showed statistical significance (p<0.05 or p<0.01) except for TYMS and TUBB3 (p>0.05); the low expression rates from high to low were ERCC1>TYMS>TUBB3>TUBB3>RRM1>BRCA1 in turn. The expression quantities of BRCA1, RRM1 and TYMS in males, smokers and patients without adenocarcinoma were all significantly higher than that in females, non-smokers and patients with adenocarcinoma, and significant differences were present (p<0.05 or p<0.01). In terms of pathological staging, the expression quantities of BRCA1, RRM1 and TYMS in phases IIa~IIb and IIIa~IIIb had a tendency to be greater than in phases I and IV.
CONCLUSIONS: Resistance to chemotherapy and sensitivity to targeted therapy differ among patients with NSCLC. Differences in gene expression in different individuals were also revealed. Only according to personalized detection results can individualized therapeutic regimens be worked out, which is a new direction for oncotherapy.

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Year:  2013        PMID: 23803067     DOI: 10.7314/apjcp.2013.14.5.2987

Source DB:  PubMed          Journal:  Asian Pac J Cancer Prev        ISSN: 1513-7368


  6 in total

1.  ERCC1 and BRCA1 mRNA expressions are associated with clinical outcome of non-small cell lung cancer treated with platinum-based chemotherapy.

Authors:  Xiuguang Qin; Wenjian Yao; Weiwei Li; Xianjun Feng; Xiaoqing Huo; Shujuan Yang; Hui Zhao; Xiaomeng Gu
Journal:  Tumour Biol       Date:  2014-01-18

2.  Prognostic value of ERCC1, RRM1, BRCA1 and SETDB1 in early stage of non-small cell lung cancer.

Authors:  A Lafuente-Sanchis; Á Zúñiga; J M Galbis; A Cremades; M Estors; N J Martínez-Hernández; J Carretero
Journal:  Clin Transl Oncol       Date:  2015-11-05       Impact factor: 3.405

3.  ERCC1, RRM1 and TUBB3 mRNA expression on the tumor response and overall survival of non-small cell lung cancer treated with platinum-based chemotherapy.

Authors:  Hongwei Qiao; Xiaoping Huang; Hua Guo; Yan Liu; Chunyan Yue
Journal:  Pak J Med Sci       Date:  2014 Nov-Dec       Impact factor: 1.088

4.  Clinical significance of UGT1A1 polymorphism and expression of ERCC1, BRCA1, TYMS, RRM1, TUBB3, STMN1 and TOP2A in gastric cancer.

Authors:  Yongkuan Cao; Guohu Zhang; Peihong Wang; Jun Zhou; Wei Gan; Yaning Song; Ling Huang; Ya Zhang; Guode Luo; Jiaqing Gong; Lin Zhang
Journal:  BMC Gastroenterol       Date:  2017-01-05       Impact factor: 3.067

5.  ERCC1 and BRCA1 mRNA expression predicts the clinical outcome of non-small cell lung cancer receiving platinum-based chemotherapy.

Authors:  Feng Xian-Jun; Qin Xiu-Guang; Zang Li; Feng Hui; Wang Wan-Ling; Liu Dong; Li Ping-Fa
Journal:  Pak J Med Sci       Date:  2014-05       Impact factor: 1.088

6.  Poor response to platinum-based chemotherapy is associated with KRAS mutation and concomitant low expression of BRAC1 and TYMS in NSCLC.

Authors:  Hongxuan Zhou; Yun Dai; Liqun Zhu; Chun Wang; Xiaodong Fei; Qin Pan; Juxiang Chen; Xianqing Shi; Yanfeng Yang; Xiaoxing Tao; Pinghuai Shi
Journal:  J Int Med Res       Date:  2016-01-05       Impact factor: 1.671

  6 in total

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