Cargando…

Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study

Metastasis-associated in colon cancer-1 (MACC1), a newly identified oncogene, is involved in angiogenesis, invasiveness, and metastasis in many cancers. Epidemiological studies have indicated the associations between MACC1 polymorphisms and cancer risk. However, the association between genetic polym...

Descripción completa

Detalles Bibliográficos
Autores principales: Dai, Zhi-Jun, Liu, Xing-Han, Kang, Hua-Feng, Wang, Xi-Jing, Jin, Tian-Bo, Zhang, Shu-Qun, Feng, Tian, Ma, Xiao-Bin, Wang, Meng, Feng, Yan-Jing, Liu, Kang, Xu, Peng, Guan, Hai-Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753940/
https://www.ncbi.nlm.nih.gov/pubmed/26871844
http://dx.doi.org/10.1097/MD.0000000000002801
_version_ 1782415944619917312
author Dai, Zhi-Jun
Liu, Xing-Han
Kang, Hua-Feng
Wang, Xi-Jing
Jin, Tian-Bo
Zhang, Shu-Qun
Feng, Tian
Ma, Xiao-Bin
Wang, Meng
Feng, Yan-Jing
Liu, Kang
Xu, Peng
Guan, Hai-Tao
author_facet Dai, Zhi-Jun
Liu, Xing-Han
Kang, Hua-Feng
Wang, Xi-Jing
Jin, Tian-Bo
Zhang, Shu-Qun
Feng, Tian
Ma, Xiao-Bin
Wang, Meng
Feng, Yan-Jing
Liu, Kang
Xu, Peng
Guan, Hai-Tao
author_sort Dai, Zhi-Jun
collection PubMed
description Metastasis-associated in colon cancer-1 (MACC1), a newly identified oncogene, is involved in angiogenesis, invasiveness, and metastasis in many cancers. Epidemiological studies have indicated the associations between MACC1 polymorphisms and cancer risk. However, the association between genetic polymorphisms in MACC1 and breast cancer (BC) was not clear. This study aimed to evaluate the relationship between MACC1 polymorphisms and BC risk. We genotyped 4 single-nucleotide polymorphisms (SNPs) in MACC1 (rs975263, rs1990172, rs3735615, rs4721888) to determine the haplotypes in 560 BC patients and 583 age-, sex-, and ethnicity-matched healthy individuals. Genotypes were determined using the Sequenom MassARRAY method. We estimated the odds ratios (ORs) and 95% confidence intervals (95% CIs) using the chi-square test. There were significant differences between patients and controls in the MACC1 rs975263 allelic (T vs C: OR = 0.76, 95% CI = 0.61–0.95, P = 0.014) and genotypic groups (TC vs TT: OR = 0.70, 95% CI = 0.54–0.92, P = 0.009; TC+CC vs TT: OR = 0.71, 95% CI = 0.55–0.92, P = 0.008). Analysis of clinical features demonstrated significant associations between rs975263 and Scarff–Bloom–Richardson (SBR) grade 3 cancer (P = 0.006) and postmenopausal women (P = 0.018). Compared with the rs4721888 CC genotype, the frequency of rs4721888 GC and GC+CC variants was higher in patients. Further analysis revealed that the variant genotypes were positively associated with lymph node metastasis. However, we failed to find any relationships between rs1990172 or rs3735615 polymorphism and BC risk. In addition, haplotype analysis indicated that the CTGG and CTCG haplotypes (rs975263, rs1990172, rs3735615, rs4721888) were significantly associated with decreased susceptibility to BC (P = 0.029 and 0.019 respectively). Our results suggest that rs975263 and rs4721888 polymorphisms in MACC1 are associated with the risk of BC susceptibility and may be involved in the progression of BC in Chinese women.
format Online
Article
Text
id pubmed-4753940
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-47539402016-02-26 Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study Dai, Zhi-Jun Liu, Xing-Han Kang, Hua-Feng Wang, Xi-Jing Jin, Tian-Bo Zhang, Shu-Qun Feng, Tian Ma, Xiao-Bin Wang, Meng Feng, Yan-Jing Liu, Kang Xu, Peng Guan, Hai-Tao Medicine (Baltimore) 3500 Metastasis-associated in colon cancer-1 (MACC1), a newly identified oncogene, is involved in angiogenesis, invasiveness, and metastasis in many cancers. Epidemiological studies have indicated the associations between MACC1 polymorphisms and cancer risk. However, the association between genetic polymorphisms in MACC1 and breast cancer (BC) was not clear. This study aimed to evaluate the relationship between MACC1 polymorphisms and BC risk. We genotyped 4 single-nucleotide polymorphisms (SNPs) in MACC1 (rs975263, rs1990172, rs3735615, rs4721888) to determine the haplotypes in 560 BC patients and 583 age-, sex-, and ethnicity-matched healthy individuals. Genotypes were determined using the Sequenom MassARRAY method. We estimated the odds ratios (ORs) and 95% confidence intervals (95% CIs) using the chi-square test. There were significant differences between patients and controls in the MACC1 rs975263 allelic (T vs C: OR = 0.76, 95% CI = 0.61–0.95, P = 0.014) and genotypic groups (TC vs TT: OR = 0.70, 95% CI = 0.54–0.92, P = 0.009; TC+CC vs TT: OR = 0.71, 95% CI = 0.55–0.92, P = 0.008). Analysis of clinical features demonstrated significant associations between rs975263 and Scarff–Bloom–Richardson (SBR) grade 3 cancer (P = 0.006) and postmenopausal women (P = 0.018). Compared with the rs4721888 CC genotype, the frequency of rs4721888 GC and GC+CC variants was higher in patients. Further analysis revealed that the variant genotypes were positively associated with lymph node metastasis. However, we failed to find any relationships between rs1990172 or rs3735615 polymorphism and BC risk. In addition, haplotype analysis indicated that the CTGG and CTCG haplotypes (rs975263, rs1990172, rs3735615, rs4721888) were significantly associated with decreased susceptibility to BC (P = 0.029 and 0.019 respectively). Our results suggest that rs975263 and rs4721888 polymorphisms in MACC1 are associated with the risk of BC susceptibility and may be involved in the progression of BC in Chinese women. Wolters Kluwer Health 2016-02-12 /pmc/articles/PMC4753940/ /pubmed/26871844 http://dx.doi.org/10.1097/MD.0000000000002801 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial License, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 3500
Dai, Zhi-Jun
Liu, Xing-Han
Kang, Hua-Feng
Wang, Xi-Jing
Jin, Tian-Bo
Zhang, Shu-Qun
Feng, Tian
Ma, Xiao-Bin
Wang, Meng
Feng, Yan-Jing
Liu, Kang
Xu, Peng
Guan, Hai-Tao
Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title_full Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title_fullStr Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title_full_unstemmed Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title_short Genetic Variation in Metastasis-Associated in Colon Cancer-1 and the Risk of Breast Cancer Among the Chinese Han Population: A STROBE-Compliant Observational Study
title_sort genetic variation in metastasis-associated in colon cancer-1 and the risk of breast cancer among the chinese han population: a strobe-compliant observational study
topic 3500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753940/
https://www.ncbi.nlm.nih.gov/pubmed/26871844
http://dx.doi.org/10.1097/MD.0000000000002801
work_keys_str_mv AT daizhijun geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT liuxinghan geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT kanghuafeng geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT wangxijing geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT jintianbo geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT zhangshuqun geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT fengtian geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT maxiaobin geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT wangmeng geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT fengyanjing geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT liukang geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT xupeng geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy
AT guanhaitao geneticvariationinmetastasisassociatedincoloncancer1andtheriskofbreastcanceramongthechinesehanpopulationastrobecompliantobservationalstudy