TY - JOUR
T1 - AA genotype of cyclin D1 G870A polymorphism increases breast cancer risk
T2 - Findings of a case-control study and meta-analysis
AU - Akhter, Naseem
AU - Alzahrani, Faisal Abdulrahman
AU - Dar, Sajad Ahmad
AU - Wahid, Mohd
AU - Sattar, Real Sumayya Abdul
AU - Hussain, Showket
AU - Haque, Shafiul
AU - Ansari, Shakeel Ahmed
AU - Jawed, Arshad
AU - Mandal, Raju K.
AU - Almalki, Shaia
AU - Alharbi, Raed A.
AU - Husain, Syed Akhtar
N1 - Publisher Copyright:
© 2019 Wiley Periodicals, Inc.
PY - 2019/10
Y1 - 2019/10
N2 - Background: Cyclin D1 (CCND1) polymorphisms, a regulator of the cell cycle progress from G1 to the S phase, may lead to uncontrolled cell proliferation and lack of apoptosis. G870A, a common single-nucleotide polymorphism in CCND1 influences breast cancer risk. However, the association between G870A polymorphism and breast cancer risk is ambiguous so far. Materials and Methods: In this case-control study, we analyzed the role of G870A polymorphism with breast cancer risk in Indian women. A meta-analysis of 18 studies was also performed to elucidate this association by increasing statistical power. Results: In our case-control study, significant risk association of the CCND1 G870A AA genotype with breast cancer in total cohort (odds ratio [OR], 2.98; 95% confidence interval [CI], 1.64-5.42; P value, 4.96e-04) and premenopausal women (OR, 3.31; 95% CI, 1.54-7.08; P value,.003) was found. The results of the meta-analysis showed that AA genotype of the CCND1 G870A polymorphism significantly increases breast cancer risk in total pooled data (AA vs GG+GA: OR = 1.20; 95% CI = 1.03 to 1.39; P value, 0.016*) and Caucasian (AA vs GG+GA: OR = 1.22; 95% CI = 0.99 to 1.51; P value,.056*) but not in Asian population. Further, a significant protective association with breast cancer was also found in the GA vs AA comparison model in pooled data (OR = 0.73; 95% CI = 0.58 to 0.92; P value,.007*) as well as in Caucasian subgroup (OR = 0.62; 95% CI = 0.49 to 0.94; P value,.022*). Conclusion: CCND1 G870A AA genotype was found associated with breast cancer risk. Future association studies considering the environmental impact on gene expression are required to validate/explore this association.
AB - Background: Cyclin D1 (CCND1) polymorphisms, a regulator of the cell cycle progress from G1 to the S phase, may lead to uncontrolled cell proliferation and lack of apoptosis. G870A, a common single-nucleotide polymorphism in CCND1 influences breast cancer risk. However, the association between G870A polymorphism and breast cancer risk is ambiguous so far. Materials and Methods: In this case-control study, we analyzed the role of G870A polymorphism with breast cancer risk in Indian women. A meta-analysis of 18 studies was also performed to elucidate this association by increasing statistical power. Results: In our case-control study, significant risk association of the CCND1 G870A AA genotype with breast cancer in total cohort (odds ratio [OR], 2.98; 95% confidence interval [CI], 1.64-5.42; P value, 4.96e-04) and premenopausal women (OR, 3.31; 95% CI, 1.54-7.08; P value,.003) was found. The results of the meta-analysis showed that AA genotype of the CCND1 G870A polymorphism significantly increases breast cancer risk in total pooled data (AA vs GG+GA: OR = 1.20; 95% CI = 1.03 to 1.39; P value, 0.016*) and Caucasian (AA vs GG+GA: OR = 1.22; 95% CI = 0.99 to 1.51; P value,.056*) but not in Asian population. Further, a significant protective association with breast cancer was also found in the GA vs AA comparison model in pooled data (OR = 0.73; 95% CI = 0.58 to 0.92; P value,.007*) as well as in Caucasian subgroup (OR = 0.62; 95% CI = 0.49 to 0.94; P value,.022*). Conclusion: CCND1 G870A AA genotype was found associated with breast cancer risk. Future association studies considering the environmental impact on gene expression are required to validate/explore this association.
KW - CCND1 G870A SNP
KW - breast cancer
KW - case-control
KW - meta-analysis
UR - https://www.scopus.com/pages/publications/85071161536
U2 - 10.1002/jcb.28800
DO - 10.1002/jcb.28800
M3 - Artículo
C2 - 31243808
AN - SCOPUS:85071161536
SN - 0730-2312
VL - 120
SP - 16452
EP - 16466
JO - Journal of Cellular Biochemistry
JF - Journal of Cellular Biochemistry
IS - 10
ER -