Association of CASP8 polymorphisms and cancer susceptibility: A meta-analysis

肿瘤科 荟萃分析 内科学 医学 联想(心理学) 全基因组关联研究 单核苷酸多态性 生物 计算生物学 基因型 遗传学 基因 心理学 心理治疗师
作者
Mohammad Hashemi,Sajjad Aftabi,Abdolkarim Moazeni‐Roodi,Hosna Sarani,Emilia Wiecheć,Saeid Ghavami
出处
期刊:European Journal of Pharmacology [Elsevier BV]
卷期号:881: 173201-173201 被引量:23
标识
DOI:10.1016/j.ejphar.2020.173201
摘要

Caspase-8 plays is an essential enzyme in apoptosis pathway. Several investigation have been done to identify the relation between CASP8 polymorphisms and different human cancers, but, the findings are still debated. The aim of the current investigation is to assess if CASP8 rs3834129 (−652 6N insertion/deletion), rs1045485 G > C, rs3769818 G > A, rs6723097 A > C, rs3769821 T > C, rs13113 T > A, rs3769825 G > A, rs2293554 A > C, and rs10931936 C > T polymorphisms are linked to susceptibility of cancer. Our team has extracted the eligible studies up to July 4, 2019, from different sources. Pooled odds ratios (ORs) with corresponding 95% confidence intervals (CIs) were estimated to quantitatively evaluate the association between CASP8 polymorphisms and cancer susceptibility. Our results showed that the rs3834129 and rs1045485 polymorphisms meaningfully reduced the risk of cancer, while the rs3769818, rs3769821 and rs3769825 polymorphisms considerably increased cancer susceptibility. No association of rs6723097, rs13113, rs2293554 and rs10931936 polymorphisms was observed with cancer susceptibility. The CASP8 rs3834129 polymorphism reduced the risk of gastrointestinal, digestive tract, colorectal, breast and lung cancers. Furthermore, the cancer risk was decreased in Asian and Caucasian populations as well as population- and hospital-based studies due to this polymorphism. There was not any relation between this gene polymorphism and the risk of prostate and cervical cancer development. Regarding the CASP8 rs1045485 polymorphism, the reduced breast cancer risk along with the risk of cancer in Caucasians, population- and hospital-based studies were observed.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
打打应助潇洒的惋清采纳,获得10
刚刚
丘比特应助潇洒的惋清采纳,获得10
1秒前
张老师发布了新的文献求助10
2秒前
3秒前
寒松发布了新的文献求助10
4秒前
4秒前
现实的幻露完成签到,获得积分10
5秒前
6秒前
思源应助潇洒的惋清采纳,获得10
7秒前
斯文败类应助潇洒的惋清采纳,获得10
8秒前
jack完成签到,获得积分10
8秒前
ding应助潇洒的惋清采纳,获得10
8秒前
lakers发布了新的文献求助10
8秒前
斯文败类应助潇洒的惋清采纳,获得10
8秒前
bkagyin应助潇洒的惋清采纳,获得10
8秒前
英姑应助潇洒的惋清采纳,获得10
8秒前
8秒前
共享精神应助郑石采纳,获得10
9秒前
慕青应助潇洒的惋清采纳,获得10
9秒前
CT完成签到,获得积分10
9秒前
9秒前
英姑应助潇洒的惋清采纳,获得10
9秒前
爆米花应助潇洒的惋清采纳,获得10
9秒前
CipherSage应助潇洒的惋清采纳,获得10
10秒前
10秒前
StrawCc完成签到 ,获得积分10
11秒前
Ddz完成签到,获得积分10
13秒前
13秒前
隐形丹珍发布了新的文献求助10
14秒前
科研通AI6.3应助朴素的愫采纳,获得10
14秒前
酷波er应助潇洒的惋清采纳,获得10
15秒前
科目三应助潇洒的惋清采纳,获得10
15秒前
田様应助潇洒的惋清采纳,获得10
15秒前
15秒前
李健应助潇洒的惋清采纳,获得10
15秒前
脑洞疼应助潇洒的惋清采纳,获得10
16秒前
16秒前
光亮的萍完成签到,获得积分10
16秒前
16秒前
SciGPT应助潇洒的惋清采纳,获得10
16秒前
高分求助中
论现代体育科学研究的方法学特征 1000
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
A Handbook of User Experience Research & Design in Libraries 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6918787
求助须知:如何正确求助?哪些是违规求助? 8609298
关于积分的说明 18265460
捐赠科研通 6333115
什么是DOI,文献DOI怎么找? 3069308
关于科研通互助平台的介绍 2098681
邀请新用户注册赠送积分活动 2046573