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Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer

Apart from other risk factors, chronic inflammation is also associated with the onset of Prostate Cancer (PCa), wherein pathogen infection and tissue microbiome dysbiosis are known to play a major role in both inflammatory response and cancer development. However, except for a few studies, the link...

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Autores principales: Sarkar, Purandar, Malik, Samaresh, Banerjee, Anwesha, Datta, Chhanda, Pal, Dilip Kumar, Ghosh, Amlan, Saha, Abhik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294280/
https://www.ncbi.nlm.nih.gov/pubmed/35865814
http://dx.doi.org/10.3389/fcimb.2022.894777
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author Sarkar, Purandar
Malik, Samaresh
Banerjee, Anwesha
Datta, Chhanda
Pal, Dilip Kumar
Ghosh, Amlan
Saha, Abhik
author_facet Sarkar, Purandar
Malik, Samaresh
Banerjee, Anwesha
Datta, Chhanda
Pal, Dilip Kumar
Ghosh, Amlan
Saha, Abhik
author_sort Sarkar, Purandar
collection PubMed
description Apart from other risk factors, chronic inflammation is also associated with the onset of Prostate Cancer (PCa), wherein pathogen infection and tissue microbiome dysbiosis are known to play a major role in both inflammatory response and cancer development. However, except for a few studies, the link between microbes and PCa remained poorly understood. To explore the potential microbiome signature associated with PCa in Indian patients, we investigated differential compositions of commensal bacteria among patients with benign prostatic hyperplasia (BPH) and PCa using 16S rRNA amplicon sequencing followed by qPCR analyses using two distinct primer sets. Using two independent cohorts, we show that Prevotella copri, Cupriavidus campinensis, and Propionibacterium acnes represent the three most abundant bacteria in diseased prostate lesions. LEfSe analyses identified that while Cupriavidus taiwanensis and Methylobacterium organophilum are distinctly elevated in PCa samples, Kocuria palustris and Cellvibrio mixtus are significantly enriched in BPH samples. Furthermore, we identify that a number of human tumor viruses, including Epstein-Barr virus (EBV) and hepatitis B virus (HBV), along with two high-risk human papillomaviruses - HPV-16 and HPV-18, are significantly associated with the PCa development and strongly correlated with PCa bacterial signature. The study may thus offer to develop a framework for exploiting this microbial signature for early diagnosis and prognosis of PCa development.
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spelling pubmed-92942802022-07-20 Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer Sarkar, Purandar Malik, Samaresh Banerjee, Anwesha Datta, Chhanda Pal, Dilip Kumar Ghosh, Amlan Saha, Abhik Front Cell Infect Microbiol Cellular and Infection Microbiology Apart from other risk factors, chronic inflammation is also associated with the onset of Prostate Cancer (PCa), wherein pathogen infection and tissue microbiome dysbiosis are known to play a major role in both inflammatory response and cancer development. However, except for a few studies, the link between microbes and PCa remained poorly understood. To explore the potential microbiome signature associated with PCa in Indian patients, we investigated differential compositions of commensal bacteria among patients with benign prostatic hyperplasia (BPH) and PCa using 16S rRNA amplicon sequencing followed by qPCR analyses using two distinct primer sets. Using two independent cohorts, we show that Prevotella copri, Cupriavidus campinensis, and Propionibacterium acnes represent the three most abundant bacteria in diseased prostate lesions. LEfSe analyses identified that while Cupriavidus taiwanensis and Methylobacterium organophilum are distinctly elevated in PCa samples, Kocuria palustris and Cellvibrio mixtus are significantly enriched in BPH samples. Furthermore, we identify that a number of human tumor viruses, including Epstein-Barr virus (EBV) and hepatitis B virus (HBV), along with two high-risk human papillomaviruses - HPV-16 and HPV-18, are significantly associated with the PCa development and strongly correlated with PCa bacterial signature. The study may thus offer to develop a framework for exploiting this microbial signature for early diagnosis and prognosis of PCa development. Frontiers Media S.A. 2022-07-05 /pmc/articles/PMC9294280/ /pubmed/35865814 http://dx.doi.org/10.3389/fcimb.2022.894777 Text en Copyright © 2022 Sarkar, Malik, Banerjee, Datta, Pal, Ghosh and Saha https://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 Cellular and Infection Microbiology
Sarkar, Purandar
Malik, Samaresh
Banerjee, Anwesha
Datta, Chhanda
Pal, Dilip Kumar
Ghosh, Amlan
Saha, Abhik
Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title_full Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title_fullStr Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title_full_unstemmed Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title_short Differential Microbial Signature Associated With Benign Prostatic Hyperplasia and Prostate Cancer
title_sort differential microbial signature associated with benign prostatic hyperplasia and prostate cancer
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294280/
https://www.ncbi.nlm.nih.gov/pubmed/35865814
http://dx.doi.org/10.3389/fcimb.2022.894777
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