中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Sox30 initiates transcription of haploid genes during late meiosis and spermiogenesis in mouse testes (vol 145, dev164855, 2018)

文献类型:期刊论文

作者Bai, Shun1; Fu, Kaiqiang1; Yin, Huiqi1; Cui, Yiqiang1; Yue, Qiuling1; Cheng, Le1; Tan, Huanhuan1; Liu, Xiaofei1; Guo, Yueshuai1; Zhang, Yingwen1
刊名DEVELOPMENT
出版日期2019
卷号146期号:10页码:UNSP dev179978
ISSN号0950-1991
DOI10.1242/dev.179978
文献子类Correction
英文摘要IMPORTANCE The causal direction and magnitude of the association between telomere length and incidence of cancer and non-neoplastic diseases is uncertain owing to the susceptibility of observational studies to confounding and reverse causation. OBJECTIVE To conduct a Mendelian randomization study, using germline genetic variants as instrumental variables, to appraise the causal relevance of telomere length for risk of cancer and non-neoplastic diseases. DATA SOURCES Genomewide association studies (GWAS) published up to January 15, 2015. STUDY SELECTION GWAS of noncommunicable diseases that assayed germline genetic variation and did not select cohort or control participants on the basis of preexisting diseases. Of 163 GWAS of noncommunicable diseases identified, summary data from 103 were available. DATA EXTRACTION AND SYNTHESIS Summary association statistics for single nucleotide polymorphisms (SNPs) that are strongly associated with telomere length in the general population. MAIN OUTCOMES AND MEASURES Odds ratios (ORs) and 95% confidence intervals (CIs) for disease per standard deviation (SD) higher telomere length due to germline genetic variation. RESULTS Summary data were available for 35 cancers and 48 non-neoplastic diseases, corresponding to 420 081 cases (median cases, 2526 per disease) and 1 093 105 controls (median, 6789 per disease). Increased telomere length due to germline genetic variation was generally associated with increased risk for site-specific cancers. The strongest associations (ORs [ 95% CIs] per 1-SD change in genetically increased telomere length) were observed for glioma, 5.27 (3.15-8.81); serous low-malignant-potential ovarian cancer, 4.35 (2.39-7.94); lung adenocarcinoma, 3.19 (2.40-4.22); neuroblastoma, 2.98 (1.92-4.62); bladder cancer, 2.19 (1.32-3.66); melanoma, 1.87 (1.55-2.26); testicular cancer, 1.76 (1.02-3.04); kidney cancer, 1.55 (1.08-2.23); and endometrial cancer, 1.31 (1.07-1.61). Associations were stronger for rarer cancers and at tissue sites with lower rates of stem cell division. There was generally little evidence of association between genetically increased telomere length and risk of psychiatric, autoimmune, inflammatory, diabetic, and other non-neoplastic diseases, except for coronary heart disease (OR, 0.78 [ 95% CI, 0.67-0.90]), abdominal aortic aneurysm (OR, 0.63 [ 95% CI, 0.49-0.81]), celiac disease (OR, 0.42 [ 95% CI, 0.28-0.61]) and interstitial lung disease (OR, 0.09 [ 95% CI, 0.05-0.15]). CONCLUSIONS AND RELEVANCE It is likely that longer telomeres increase risk for several cancers but reduce risk for some non-neoplastic diseases, including cardiovascular diseases.
学科主题Developmental Biology
语种英语
WOS记录号WOS:000470963700014
出版者COMPANY BIOLOGISTS LTD
版本出版稿
源URL[http://202.127.25.144/handle/331004/1012]  
专题中国科学院上海生命科学研究院营养科学研究所
作者单位1.Nanjing Med Univ, State Key Lab Reprod Med, Nanjing 211166, Jiangsu, Peoples R China;
2.Baylor Coll Med, Dept Med, Houston, TX 77030 USA;
3.Nanjing Med Univ, Sch Basic Med Sci, Dept Neurobiol, Nanjing 211166, Jiangsu, Peoples R China;
4.Chinese Acad Sci, Shanghai Inst Biol Sci, CAS MPG Partner Inst Computat Biol, Omics Core Biomed Big Data Ctr, Shanghai 200031, Peoples R China,
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Bai, Shun,Fu, Kaiqiang,Yin, Huiqi,et al. Sox30 initiates transcription of haploid genes during late meiosis and spermiogenesis in mouse testes (vol 145, dev164855, 2018)[J]. DEVELOPMENT,2019,146(10):UNSP dev179978.
APA Bai, Shun.,Fu, Kaiqiang.,Yin, Huiqi.,Cui, Yiqiang.,Yue, Qiuling.,...&,.(2019).Sox30 initiates transcription of haploid genes during late meiosis and spermiogenesis in mouse testes (vol 145, dev164855, 2018).DEVELOPMENT,146(10),UNSP dev179978.
MLA Bai, Shun,et al."Sox30 initiates transcription of haploid genes during late meiosis and spermiogenesis in mouse testes (vol 145, dev164855, 2018)".DEVELOPMENT 146.10(2019):UNSP dev179978.

入库方式: OAI收割

来源:上海营养与健康研究所

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