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AURKA rs2273535 T>A Polymorphism Associated With Cancer Risk: A Systematic Review With Meta-Analysis.
Wang, Shujie; Qi, Jian; Zhu, Meiling; Wang, Meng; Nie, Jinfu.
Affiliation
  • Wang S; Anhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
  • Qi J; Hefei Cancer Hospital, Chinese Academy of Sciences, Hefei, China.
  • Zhu M; Anhui Province Key Laboratory of Medical Physics and Technology, Center of Medical Physics and Technology, Hefei Institutes of Physical Science, Chinese Academy of Sciences, Hefei, China.
  • Wang M; Hefei Cancer Hospital, Chinese Academy of Sciences, Hefei, China.
  • Nie J; Department of Oncology, Xinhua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Front Oncol ; 10: 1040, 2020.
Article in En | MEDLINE | ID: mdl-32733797
ABSTRACT
Aurora kinase A (AURKA) is a cell cycle regulatory serine/threonine kinase that promotes cell cycle progression. It plays an important role in regulating the transition from G2 to M phase during mitosis. The association between the AURKA rs2273535 T>A polymorphism and cancer risk has been investigated, but the results remain inconsistent. To get a more accurate conclusion, we conducted a comprehensive meta-analysis of 36 case-control studies, involving 22,884 cancer cases and 30,497 healthy controls. Crude odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to determine the association of interest. Pooled analysis indicated that the AURKA rs2273535 T>A polymorphism increased the overall risk of cancer (homozygous OR = 1.17, 95% CI = 1.04-1.33; recessive OR = 1.15, 95% CI = 1.05-1.25; allele OR = 1.07, 95% CI = 1.02-1.13). Stratification analysis by cancer type further showed that this polymorphism was associated with an increased breast cancer risk. This meta-analysis indicated that the AURKA rs2273535 T>A polymorphism was associated with an overall increased cancer risk, especially breast cancer. Further validation experiments are needed to strengthen our conclusion.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Language: En Journal: Front Oncol Year: 2020 Document type: Article Affiliation country: China Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Etiology_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Language: En Journal: Front Oncol Year: 2020 Document type: Article Affiliation country: China Publication country: CH / SUIZA / SUÍÇA / SWITZERLAND