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Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening

BACKGROUND: Breast and ovarian cancers are the most prevalent cancers and one of the leading causes of death in Indian women. The healthcare burden of breast and ovarian cancers and the rise in mortality rate are worrying and stress the need for early detection and treatment. METHODS: We performed a...

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Autores principales: Kadri, Mohammed Shaad N., Patel, Komal M., Bhargava, Poonam A., Shah, Franky D., Badgujar, Nutan V., Tarapara, Bhoomi V., Patel, Prabhudas S., Shaikh, Mohammed Inayatullah, Shah, Krati, Patel, Apurva, Pandya, Shashank, Vora, Hemangini, Joshi, Chaitanya G., Joshi, Madhvi N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859489/
https://www.ncbi.nlm.nih.gov/pubmed/33552952
http://dx.doi.org/10.3389/fonc.2020.568786
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author Kadri, Mohammed Shaad N.
Patel, Komal M.
Bhargava, Poonam A.
Shah, Franky D.
Badgujar, Nutan V.
Tarapara, Bhoomi V.
Patel, Prabhudas S.
Shaikh, Mohammed Inayatullah
Shah, Krati
Patel, Apurva
Pandya, Shashank
Vora, Hemangini
Joshi, Chaitanya G.
Joshi, Madhvi N.
author_facet Kadri, Mohammed Shaad N.
Patel, Komal M.
Bhargava, Poonam A.
Shah, Franky D.
Badgujar, Nutan V.
Tarapara, Bhoomi V.
Patel, Prabhudas S.
Shaikh, Mohammed Inayatullah
Shah, Krati
Patel, Apurva
Pandya, Shashank
Vora, Hemangini
Joshi, Chaitanya G.
Joshi, Madhvi N.
author_sort Kadri, Mohammed Shaad N.
collection PubMed
description BACKGROUND: Breast and ovarian cancers are the most prevalent cancers and one of the leading causes of death in Indian women. The healthcare burden of breast and ovarian cancers and the rise in mortality rate are worrying and stress the need for early detection and treatment. METHODS: We performed amplicon sequencing of 144 cases who had breast/ovarian cancer disease (total 137 cases are patients and seven are tested for BRCA1/2 carrier) Using our custom designed gene panel consisting of 14 genes, that are associated with high to moderate risk of breast and ovarian cancers. Variants were called using Torrent Variant Caller and were annotated using ThermoFisher’s Ion Reporter software. Classification of variants and their clinical significance were identified by searching the variants against ClinVar database. RESULTS: From a total of 144 cases, we were able to detect 42 pathogenic mutations in [40/144] cases. Majority of pathogenic mutations (30/41) were detected in BRCA1 gene, while (7/41) pathogenic mutations were detected in BRCA2 gene, whereas, (2/41) pathogenic mutations were detected in TP53 gene and BRIP1, PALB2, and ATM genes respectively. So, BRCA genes contributed 88.09% of pathogenic mutations, whereas non-BRCA genes contributed 11.91% of pathogenic mutations. We were also able to detect 25 VUS which were predicted to be damaging by in silico prediction tools. CONCLUSION: Early detection of cancers in the Indian population can be done by genetic screening using customized multi-gene panels. Indications of our findings show that in the Indian population, apart from the common BRCA genes, there are other genes that are also responsible for the disease. High frequency mutations detected in the study and variants of uncertain significance predicted to be damaging by in silico pathogenicity prediction tools can be potential biomarkers of hereditary breast and ovarian cancer in Indian HBOC patients.
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spelling pubmed-78594892021-02-05 Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening Kadri, Mohammed Shaad N. Patel, Komal M. Bhargava, Poonam A. Shah, Franky D. Badgujar, Nutan V. Tarapara, Bhoomi V. Patel, Prabhudas S. Shaikh, Mohammed Inayatullah Shah, Krati Patel, Apurva Pandya, Shashank Vora, Hemangini Joshi, Chaitanya G. Joshi, Madhvi N. Front Oncol Oncology BACKGROUND: Breast and ovarian cancers are the most prevalent cancers and one of the leading causes of death in Indian women. The healthcare burden of breast and ovarian cancers and the rise in mortality rate are worrying and stress the need for early detection and treatment. METHODS: We performed amplicon sequencing of 144 cases who had breast/ovarian cancer disease (total 137 cases are patients and seven are tested for BRCA1/2 carrier) Using our custom designed gene panel consisting of 14 genes, that are associated with high to moderate risk of breast and ovarian cancers. Variants were called using Torrent Variant Caller and were annotated using ThermoFisher’s Ion Reporter software. Classification of variants and their clinical significance were identified by searching the variants against ClinVar database. RESULTS: From a total of 144 cases, we were able to detect 42 pathogenic mutations in [40/144] cases. Majority of pathogenic mutations (30/41) were detected in BRCA1 gene, while (7/41) pathogenic mutations were detected in BRCA2 gene, whereas, (2/41) pathogenic mutations were detected in TP53 gene and BRIP1, PALB2, and ATM genes respectively. So, BRCA genes contributed 88.09% of pathogenic mutations, whereas non-BRCA genes contributed 11.91% of pathogenic mutations. We were also able to detect 25 VUS which were predicted to be damaging by in silico prediction tools. CONCLUSION: Early detection of cancers in the Indian population can be done by genetic screening using customized multi-gene panels. Indications of our findings show that in the Indian population, apart from the common BRCA genes, there are other genes that are also responsible for the disease. High frequency mutations detected in the study and variants of uncertain significance predicted to be damaging by in silico pathogenicity prediction tools can be potential biomarkers of hereditary breast and ovarian cancer in Indian HBOC patients. Frontiers Media S.A. 2021-01-21 /pmc/articles/PMC7859489/ /pubmed/33552952 http://dx.doi.org/10.3389/fonc.2020.568786 Text en Copyright © 2021 Kadri, Patel, Bhargava, Shah, Badgujar, Tarapara, Patel, Shaikh, Shah, Patel, Pandya, Vora, Joshi and Joshi http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Kadri, Mohammed Shaad N.
Patel, Komal M.
Bhargava, Poonam A.
Shah, Franky D.
Badgujar, Nutan V.
Tarapara, Bhoomi V.
Patel, Prabhudas S.
Shaikh, Mohammed Inayatullah
Shah, Krati
Patel, Apurva
Pandya, Shashank
Vora, Hemangini
Joshi, Chaitanya G.
Joshi, Madhvi N.
Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title_full Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title_fullStr Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title_full_unstemmed Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title_short Mutational Landscape for Indian Hereditary Breast and Ovarian Cancer Cohort Suggests Need for Identifying Population Specific Genes and Biomarkers for Screening
title_sort mutational landscape for indian hereditary breast and ovarian cancer cohort suggests need for identifying population specific genes and biomarkers for screening
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7859489/
https://www.ncbi.nlm.nih.gov/pubmed/33552952
http://dx.doi.org/10.3389/fonc.2020.568786
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