Methylenetetrahydrofolate reductase polymorphisms and colorectal cancer prognosis: A meta-analysis

被引:9
作者
Chen, Xin-Lin [1 ]
Wang, Yu-Mei [2 ]
Zhao, Fei [1 ]
Chen, Zheng [3 ]
Yang, Xiaofei [4 ]
Sun, Cong [5 ]
Gao, Yunpeng [6 ]
Yang, Tian-Ge [7 ]
Tian, Guo [7 ]
Chen, Yi-Ming [1 ]
Zhu, Shui-Lian [8 ]
Lin, Xiao-Bing [9 ]
Liu, Feng-Bin [8 ]
机构
[1] Guangzhou Univ Chinese Med, Sch Basic Med Sci, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangzhou Univ Chinese Med, Sch Chinese Mat Med, Dept Pharmacol, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 3, Guangzhou, Guangdong, Peoples R China
[4] Guangzhou Univ Chinese Med, Clin Coll 2, Guangzhou, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Zhongshan Sch Med, Guangzhou, Guangdong, Peoples R China
[6] Univ Texas Southwestern Med Ctr Dallas, Eugene McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA
[7] Guangzhou Univ Chinese Med, Sch Acupuncture & Rehabil, Guangzhou, Guangdong, Peoples R China
[8] Guangzhou Univ Chinese Med, Affiliated Hosp 1, Clin Coll 1, Guangzhou, Guangdong, Peoples R China
[9] Guangzhou Univ Chinese Med, Personnel Dept, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
colorectal cancer; gene polymorphism; meta-analysis; methylenetetrahydrofolate reductase; prognosis; FLUOROURACIL-BASED TREATMENT; MTHFR GENE POLYMORPHISMS; ADJUVANT CHEMOTHERAPY; FOLFOX CHEMOTHERAPY; C677T POLYMORPHISM; FOLATE METABOLISM; STAGE-II; SURVIVAL; ASSOCIATION; A1298C;
D O I
10.1002/jgm.3114
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background The present study focused on understanding the prognostic value of the methylenetetrahydrofolate reductase (MTHFR) single nucleotide polymorphisms rs1801133 (C667T) and rs1801131 (A1298C) in patients with colorectal cancer (CRC). Methods A systematic literature search was conducted in March 2016. Databases, including Medline, EMBASE, Cochrane and Chinese databases (including CNKI, Wanfang and VIP), were searched to identify the relevant articles describing MTHFR polymorphisms in patients with CRC. Data regarding overall survival (OS), progression-free survival (PFS) and disease-free survival (DFS) were collected and analysed. Results Twenty-four studies with 5423 patients with CRC were included. Significant differences in OS, PFS and DFS were not observed among the different comparisons of patients carrying different alleles of the MTHFR rs1801133 polymorphism (including TT versus CC, TT versus CT + CC, CT + TT versus CC and CT versus CC). Compared with patients with the rs1801131 CA + AA genotypes, patients with the CC genotype had a shorter OS (hazard ratio = 1.85; 95% confidence interval = 1.30-2.65) and DFS (hazard ratio = 2.16; 95% confidence interval= 1.19-3.93). Significant differences in OS, PFS and DFS were not observed among the other patient groups (including CC versus AA, CC + CA versus AA and CA versus AA). Subgroup analysis of rs1801133 and rs1801131 showed that patients with CRC from Asian regions and Western regions demonstrated similar results. Conclusions The MTHFR rs1801133 polymorphism was not associated with the prognosis of patients with CRC; however, rs1801131 may be associated with the prognosis of patients with CRC. Well-designed prospective studies are necessary to obtain a better understanding of the prognostic value of rs1801133 and rs1801131.
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页数:10
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