MTHFR 677C>T多态性与培美曲塞化疗对晚期NSCLC疗效的相关性:一项荟萃分析

IF 0.5 4区 医学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Pteridines Pub Date : 2021-01-01 DOI:10.1515/pteridines-2020-0026
Feng Han, Wengui Xu
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引用次数: 1

摘要

摘要目的通过汇集已公开发表的相关研究,探讨MTHFR 677C>T多态性与培美曲塞化疗对晚期非小细胞肺癌癌症(NSCLC)疗效的相关性。方法系统检索Pubmed、Embase、Cochrance Library、CNKI和Wanfang等数据库中MTHFR677C>T多态性及培美曲塞化疗对晚期NSCLC疗效的临床研究。相关性用比值比(OR)和相应的95%置信区间(95%CI)表示。纳入研究的发表偏倚通过Begg漏斗图和Egger线性回归检验进行评估。结果本荟萃分析纳入了10项与MTHFR 677C>T多态性和培美曲塞化疗在NSCLC中的疗效相关的前瞻性临床研究。汇总结果表明,在显性基因模型中,TT或CT基因型的NSCLC患者的部分反应低于CC基因型(TT+CT vs CC)(or=0.16,95%CI:0.06–0.41,P=0.001)。以培美曲塞为基础的显性化疗的客观反应率低于C基因型(or=0.28,95%CI:0.18–0.45,P=0.001,隐性(OR=0.43,95%CI:0.19-0.94,P=0.03)和纯合模型(OR=0.30,95%CI:0.13-0.67,P=0.003)。但不同基因型和不同基因型模型的疾病控制率和疾病进展率无统计学差异(P>0.05),其可作为潜在的基于培美曲塞的化疗反应标志物应用。
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Correlation between MTHFR 677C > T polymorphism and response of pemetrexed-based chemotherapy in advanced NSCLC: A meta-analysis
Abstract Objective The aim of this study was to investigate the correlation between MTHFR 677C > T polymorphism and response of pemetrexed-based chemotherapy in advanced non-small-cell lung cancer (NSCLC) by pooling the open published relevant studies. Methods Clinical studies associated with MTHFR 677C > T polymorphism and response of pemetrexed-based chemotherapy in advanced NSCLC were systematically searched in databases of Pubmed, Embase, Cochrance Library, China national knowledge infrastructure (CNKI) and Wanfang. The correlation was expressed by odds ratio (OR) and corresponding 95% confidence interval (95% CI). The publication bias of the included studies was evaluated through Begg’s funnel plot and Egger’s line regression test. Results Ten prospective clinical studies relevant to MTHFR 677C > T polymorphism and response of pemetrexed-based chemotherapy in NSCLC were included in the present meta-analysis. The pooled results indicated that the partial response in NSCLC patients with TT or CT genotype was inferior to CC genotype in a dominant gene model (TT + CT vs CC) (OR = 0.16, 95% CI: 0.06–0.41, P = 0.001). NSCLC cases with T genotype were inferior to C genotype in the objective response rate treated with pemetrexed-based chemotherapy for dominant (OR = 0.28, 95% CI: 0.18–0.45, P = 0.001), recessive (OR = 0.43, 95% CI: 0.19–0.94, P = 0.03) and homozygous models (OR = 0.30, 95% CI: 0.13–0.67, P = 0.003). However, there was no statistical difference in disease control rate, progressive disease between different genotypes of different gene models (P all > 0.05). Conclusion The pemetrexed-based chemotherapy response was decreased in NSCLC cases with T genotype, which can be applied as a potential pemetrexed-based chemotherapy response marker.
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来源期刊
Pteridines
Pteridines 生物-生化与分子生物学
CiteScore
1.20
自引率
25.00%
发文量
6
审稿时长
>12 weeks
期刊介绍: Pteridines is an open acess international quarterly journal dealing with all aspects of pteridine research. Pteridines are heterocyclic fused ring compounds involved in a wide range of biological functions from the color on butterfly wings to cofactors in enzyme catalysis to essential vitamins. Of the pteridines, 5,6,7,8-tetrahydrobiopterin is the necessary cofactor of several aromatic amino acid monoxygenases, the nitric oxide synthases and glyceryl ether monoxygenase (GEMO). Neopterin plays an essential role in the immune system and is an important biomarker in laboratory medicine for diseases such as HIV, cardiovascular disease, malignant tumors, among others. Topics: -Neopterin, dihydroneopterin, monapterin- Biopterin, tetrahydrobiopterin- Folates, antifolates, riboflavin- Phenylalanine, tyrosine, phenylketonuria, serotonin, adrenalin, noradrenalin, L-DOPA, dopamine, related biogenic amines- Phenylalanine hydroxylase, tyrosine hydroxylase, tryptophan hydroxylase, nitric oxide synthases (iNOS), alkylglycerol monooxygenase (AGMO), dihydropterin reductase, sepiapterin reductase- Homocysteine, mediators of inflammation, redox systems, iron.
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