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Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer

BACKGROUND: Extracellular matrix degradation by matrix metalloproteinases (MMPs) is an important mechanism involved in tumor invasion and metastasis. Genetic variations of MMPs have shown association with multiple cancers. The present study is focused to elucidate the association of MMP-1, 3 and 9 g...

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Autores principales: Padala, Chiranjeevi, Tupurani, Mohini Aiyengar, Puranam, Kaushik, Gantala, Srilatha, Shyamala, Nivas, Kondapalli, Mrudula Spurthi, Gundapaneni, Kishore kumar, Mudigonda, Saraswati, Galimudi, Rajesh Kumar, Kupsal, Keerthi, Nanchari, Santoshi Rani, Chavan, Uday, Chinta, Sanjeeva kumari, Mukta, Srinivasulu, Satti, Vishnupriya, Hanumanth, Surekha Rani
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621673/
https://www.ncbi.nlm.nih.gov/pubmed/28961241
http://dx.doi.org/10.1371/journal.pone.0184448
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author Padala, Chiranjeevi
Tupurani, Mohini Aiyengar
Puranam, Kaushik
Gantala, Srilatha
Shyamala, Nivas
Kondapalli, Mrudula Spurthi
Gundapaneni, Kishore kumar
Mudigonda, Saraswati
Galimudi, Rajesh Kumar
Kupsal, Keerthi
Nanchari, Santoshi Rani
Chavan, Uday
Chinta, Sanjeeva kumari
Mukta, Srinivasulu
Satti, Vishnupriya
Hanumanth, Surekha Rani
author_facet Padala, Chiranjeevi
Tupurani, Mohini Aiyengar
Puranam, Kaushik
Gantala, Srilatha
Shyamala, Nivas
Kondapalli, Mrudula Spurthi
Gundapaneni, Kishore kumar
Mudigonda, Saraswati
Galimudi, Rajesh Kumar
Kupsal, Keerthi
Nanchari, Santoshi Rani
Chavan, Uday
Chinta, Sanjeeva kumari
Mukta, Srinivasulu
Satti, Vishnupriya
Hanumanth, Surekha Rani
author_sort Padala, Chiranjeevi
collection PubMed
description BACKGROUND: Extracellular matrix degradation by matrix metalloproteinases (MMPs) is an important mechanism involved in tumor invasion and metastasis. Genetic variations of MMPs have shown association with multiple cancers. The present study is focused to elucidate the association of MMP-1, 3 and 9 genetic variants with respect to epidemiological and clinicopathological variables by haplotype, LD, MDR, survival in silico analyses among South Indian women. MATERIAL AND METHODS: MMP3–1171 5A/6A and MMP9–1562 C/T SNPs were genotyped by Allele specific polymerase chain reaction and MMP1-1607 1G/2G polymorphism by restriction fragment length polymorphism assays respectively, in 300 BC patients and age-matched 300 healthy controls. Statistical analysis was performed using the SNPStats and SPSS software. Linkage disequilibrium and gene-gene interactions were performed using Haploview and MDR software respectively. Further, transcription factor binding sites in the promoter regions of SNPs under study were carried out using AliBaba2.1 software. RESULTS: We have observed an increased frequency of 2G-allele of MMP1, 6A-allele of MMP3 and T-allele of MMP9 (p<0.05) respectively in BC subjects. The 2G-6A haplotype (minor alleles of MMP-1 and MMP-3 respectively) has shown an increased susceptibility to BC. Further, MMP polymorphisms were associated with the clinical characteristics of BC patients such as steroid hormone receptor status, lymph node involvement and metastasis. SNP combinations were in perfect LD in controls. MDR analysis revealed a positive interaction between the SNPs. 5-years survival rate and cox-regression analysis showed a significant association with clinicopathological variables. CONCLUSION: Our results suggest that MMP1–1607 1G/2G, MMP3–1171 5A/6A and MMP9–1562 C/T gene polymorphisms have synergistic effect on breast cancer. The interactions of MMPs clinical risk factors such as lymph node involvement has shown a strong correlation and might influence the 5-years survival rate, suggesting their potential role in the breast carcinogenesis.
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spelling pubmed-56216732017-10-17 Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer Padala, Chiranjeevi Tupurani, Mohini Aiyengar Puranam, Kaushik Gantala, Srilatha Shyamala, Nivas Kondapalli, Mrudula Spurthi Gundapaneni, Kishore kumar Mudigonda, Saraswati Galimudi, Rajesh Kumar Kupsal, Keerthi Nanchari, Santoshi Rani Chavan, Uday Chinta, Sanjeeva kumari Mukta, Srinivasulu Satti, Vishnupriya Hanumanth, Surekha Rani PLoS One Research Article BACKGROUND: Extracellular matrix degradation by matrix metalloproteinases (MMPs) is an important mechanism involved in tumor invasion and metastasis. Genetic variations of MMPs have shown association with multiple cancers. The present study is focused to elucidate the association of MMP-1, 3 and 9 genetic variants with respect to epidemiological and clinicopathological variables by haplotype, LD, MDR, survival in silico analyses among South Indian women. MATERIAL AND METHODS: MMP3–1171 5A/6A and MMP9–1562 C/T SNPs were genotyped by Allele specific polymerase chain reaction and MMP1-1607 1G/2G polymorphism by restriction fragment length polymorphism assays respectively, in 300 BC patients and age-matched 300 healthy controls. Statistical analysis was performed using the SNPStats and SPSS software. Linkage disequilibrium and gene-gene interactions were performed using Haploview and MDR software respectively. Further, transcription factor binding sites in the promoter regions of SNPs under study were carried out using AliBaba2.1 software. RESULTS: We have observed an increased frequency of 2G-allele of MMP1, 6A-allele of MMP3 and T-allele of MMP9 (p<0.05) respectively in BC subjects. The 2G-6A haplotype (minor alleles of MMP-1 and MMP-3 respectively) has shown an increased susceptibility to BC. Further, MMP polymorphisms were associated with the clinical characteristics of BC patients such as steroid hormone receptor status, lymph node involvement and metastasis. SNP combinations were in perfect LD in controls. MDR analysis revealed a positive interaction between the SNPs. 5-years survival rate and cox-regression analysis showed a significant association with clinicopathological variables. CONCLUSION: Our results suggest that MMP1–1607 1G/2G, MMP3–1171 5A/6A and MMP9–1562 C/T gene polymorphisms have synergistic effect on breast cancer. The interactions of MMPs clinical risk factors such as lymph node involvement has shown a strong correlation and might influence the 5-years survival rate, suggesting their potential role in the breast carcinogenesis. Public Library of Science 2017-09-29 /pmc/articles/PMC5621673/ /pubmed/28961241 http://dx.doi.org/10.1371/journal.pone.0184448 Text en © 2017 Padala et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Padala, Chiranjeevi
Tupurani, Mohini Aiyengar
Puranam, Kaushik
Gantala, Srilatha
Shyamala, Nivas
Kondapalli, Mrudula Spurthi
Gundapaneni, Kishore kumar
Mudigonda, Saraswati
Galimudi, Rajesh Kumar
Kupsal, Keerthi
Nanchari, Santoshi Rani
Chavan, Uday
Chinta, Sanjeeva kumari
Mukta, Srinivasulu
Satti, Vishnupriya
Hanumanth, Surekha Rani
Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title_full Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title_fullStr Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title_full_unstemmed Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title_short Synergistic effect of collagenase-1 (MMP1), stromelysin-1 (MMP3) and gelatinase-B (MMP9) gene polymorphisms in breast cancer
title_sort synergistic effect of collagenase-1 (mmp1), stromelysin-1 (mmp3) and gelatinase-b (mmp9) gene polymorphisms in breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621673/
https://www.ncbi.nlm.nih.gov/pubmed/28961241
http://dx.doi.org/10.1371/journal.pone.0184448
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