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Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing
Breast cancer (BC) has emerged as the most common malignancy among females. The genomic profile of BC is diverse in nature and complex due to heterogeneity among various geographically different ethnic groups. The primary objective of this study was to carry out a comprehensive mutational analysis o...
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Published in: | Scientific reports 2024-08, Vol.14 (1), p.18679-11, Article 18679 |
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creator | Kumar, Rahul Awasthi, Supriya Pradhan, Dibyabhaba Kumar, Rakesh Goel, Harsh Singh, Jay Haider, Imran Deo, S. V. S. Kumar, Chitresh Srivastava, Anurag Bhatnagar, Amar Kumar, Rakesh Lakshmi, S. Augustine, Paul Ranjan, Amar Chopra, Anita Gogia, Ajay Batra, Atul Mathur, Sandeep Rath, Goura Kishor Kaur, Tanvir Dhaliwal, R. S. Mathew, Aleyamma Agrawal, Usha Hussain, Showket Tanwar, Pranay |
description | Breast cancer (BC) has emerged as the most common malignancy among females. The genomic profile of BC is diverse in nature and complex due to heterogeneity among various geographically different ethnic groups. The primary objective of this study was to carry out a comprehensive mutational analysis of Indian BC cases by performing whole exome sequencing. The cohort included patients with a median age of 48 years. TTN, TP53, MUC16, SYNE1, and OBSCN were the frequently altered genes found in our cohort. The PIK3CA and KLC3 genes are driver genes implicated in various cellular functions and cargo transportation through microtubules, respectively. Except for CCDC168 and PIK3CA, several gene pairings were found to be significantly linked with co-occurrence. Irrespective of their hormonal receptor status, RTK/RAS was observed with frequently altered signaling pathways. Further analysis of the mutational signature revealed that SBS13, SBS6, and SBS29 were mainly observed in our cohort. This study supplements the discovery of diagnostic biomarkers and provides new therapeutic options for the improved management of BC. |
doi_str_mv | 10.1038/s41598-024-65148-4 |
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The genomic profile of BC is diverse in nature and complex due to heterogeneity among various geographically different ethnic groups. The primary objective of this study was to carry out a comprehensive mutational analysis of Indian BC cases by performing whole exome sequencing. The cohort included patients with a median age of 48 years. TTN, TP53, MUC16, SYNE1, and OBSCN were the frequently altered genes found in our cohort. The PIK3CA and KLC3 genes are driver genes implicated in various cellular functions and cargo transportation through microtubules, respectively. Except for CCDC168 and PIK3CA, several gene pairings were found to be significantly linked with co-occurrence. Irrespective of their hormonal receptor status, RTK/RAS was observed with frequently altered signaling pathways. Further analysis of the mutational signature revealed that SBS13, SBS6, and SBS29 were mainly observed in our cohort. This study supplements the discovery of diagnostic biomarkers and provides new therapeutic options for the improved management of BC.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/s41598-024-65148-4</identifier><identifier>PMID: 39134585</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/67 ; 692/308 ; 692/4028 ; Adult ; Aged ; Biomarkers, Tumor - genetics ; Breast cancer ; Breast Neoplasms - genetics ; DNA Mutational Analysis ; Driver gene ; Exome Sequencing ; Female ; Genomic analysis ; Heterogeneity ; Humanities and Social Sciences ; Humans ; India - epidemiology ; Malignancy ; Microtubules ; Middle Aged ; Minority & ethnic groups ; multidisciplinary ; Mutation ; Oncogenic pathway ; p53 Protein ; SBS signature ; Science ; Science (multidisciplinary) ; Whole genome sequencing ; Whole-exome sequencing</subject><ispartof>Scientific reports, 2024-08, Vol.14 (1), p.18679-11, Article 18679</ispartof><rights>The Author(s) 2024</rights><rights>2024. 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V. S.</creatorcontrib><creatorcontrib>Kumar, Chitresh</creatorcontrib><creatorcontrib>Srivastava, Anurag</creatorcontrib><creatorcontrib>Bhatnagar, Amar</creatorcontrib><creatorcontrib>Kumar, Rakesh</creatorcontrib><creatorcontrib>Lakshmi, S.</creatorcontrib><creatorcontrib>Augustine, Paul</creatorcontrib><creatorcontrib>Ranjan, Amar</creatorcontrib><creatorcontrib>Chopra, Anita</creatorcontrib><creatorcontrib>Gogia, Ajay</creatorcontrib><creatorcontrib>Batra, Atul</creatorcontrib><creatorcontrib>Mathur, Sandeep</creatorcontrib><creatorcontrib>Rath, Goura Kishor</creatorcontrib><creatorcontrib>Kaur, Tanvir</creatorcontrib><creatorcontrib>Dhaliwal, R. 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The PIK3CA and KLC3 genes are driver genes implicated in various cellular functions and cargo transportation through microtubules, respectively. Except for CCDC168 and PIK3CA, several gene pairings were found to be significantly linked with co-occurrence. Irrespective of their hormonal receptor status, RTK/RAS was observed with frequently altered signaling pathways. Further analysis of the mutational signature revealed that SBS13, SBS6, and SBS29 were mainly observed in our cohort. This study supplements the discovery of diagnostic biomarkers and provides new therapeutic options for the improved management of BC.</description><subject>631/67</subject><subject>692/308</subject><subject>692/4028</subject><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers, Tumor - genetics</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>DNA Mutational Analysis</subject><subject>Driver gene</subject><subject>Exome Sequencing</subject><subject>Female</subject><subject>Genomic analysis</subject><subject>Heterogeneity</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>India - epidemiology</subject><subject>Malignancy</subject><subject>Microtubules</subject><subject>Middle Aged</subject><subject>Minority & ethnic groups</subject><subject>multidisciplinary</subject><subject>Mutation</subject><subject>Oncogenic pathway</subject><subject>p53 Protein</subject><subject>SBS signature</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Whole genome sequencing</subject><subject>Whole-exome sequencing</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kk1v1DAQhiMEolXpH-CALHHhEvBn1j4hVEFZqRIHQOJmje3JNqvEXuxsof--7qaUlgO-jOV5_dgz8zbNS0bfMir0uyKZMrqlXLadYlK38klzzKlULRecP32wP2pOS9nSuhQ3kpnnzZEwTEil1XHz42uaYB48mfZzjSnCSEaIoXjYIQGfUylkHcMAkbiMUGbiIXrMNRQsxF2TX5dpRIK_04Sk4M89Rj_EzYvmWQ9jwdO7eNJ8__Tx29nn9uLL-frsw0XrJedz23XMSMGF9p1Q3kMvNdVScxMkME2F6wNdObMKxmDvHEhARhnThofAnUJx0qwXbkiwtbs8TJCvbYLBHg5S3ljItcARbWAGRd97EMFLcOB6qpBqz0FQ57CvrPcLa7d3EwaPcc4wPoI-zsTh0m7SlWVMMNOteCW8uSPkVDtRZjsNxeNYW4ppX6yghouuk1JV6et_pNu0z7X_i4oJYcQtkC-qwyQy9ve_YdTeGsEuRrDVCPZgBCvrpVcP67i_8mfsVSAWQampuMH89-3_YG8ADSW_rw</recordid><startdate>20240812</startdate><enddate>20240812</enddate><creator>Kumar, Rahul</creator><creator>Awasthi, Supriya</creator><creator>Pradhan, Dibyabhaba</creator><creator>Kumar, Rakesh</creator><creator>Goel, Harsh</creator><creator>Singh, Jay</creator><creator>Haider, Imran</creator><creator>Deo, S. 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The genomic profile of BC is diverse in nature and complex due to heterogeneity among various geographically different ethnic groups. The primary objective of this study was to carry out a comprehensive mutational analysis of Indian BC cases by performing whole exome sequencing. The cohort included patients with a median age of 48 years. TTN, TP53, MUC16, SYNE1, and OBSCN were the frequently altered genes found in our cohort. The PIK3CA and KLC3 genes are driver genes implicated in various cellular functions and cargo transportation through microtubules, respectively. Except for CCDC168 and PIK3CA, several gene pairings were found to be significantly linked with co-occurrence. Irrespective of their hormonal receptor status, RTK/RAS was observed with frequently altered signaling pathways. Further analysis of the mutational signature revealed that SBS13, SBS6, and SBS29 were mainly observed in our cohort. 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subjects | 631/67 692/308 692/4028 Adult Aged Biomarkers, Tumor - genetics Breast cancer Breast Neoplasms - genetics DNA Mutational Analysis Driver gene Exome Sequencing Female Genomic analysis Heterogeneity Humanities and Social Sciences Humans India - epidemiology Malignancy Microtubules Middle Aged Minority & ethnic groups multidisciplinary Mutation Oncogenic pathway p53 Protein SBS signature Science Science (multidisciplinary) Whole genome sequencing Whole-exome sequencing |
title | Somatic mutational landscape across Indian breast cancer cases by whole exome sequencing |
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