Cargando…

The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers

SIMPLE SUMMARY: The cancer microbiome has been suggested to be closely involved in the immune dysregulation that leads to carcinogenesis. Given that pancreatic adenocarcinoma (PAAD) is one of the most lethal cancers, it is important to identify features of the microbiome that may contribute to more...

Descripción completa

Detalles Bibliográficos
Autores principales: Chakladar, Jaideep, Kuo, Selena Z., Castaneda, Grant, Li, Wei Tse, Gnanasekar, Aditi, Yu, Michael Andrew, Chang, Eric Y., Wang, Xiao Qi, Ongkeko, Weg M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565819/
https://www.ncbi.nlm.nih.gov/pubmed/32962112
http://dx.doi.org/10.3390/cancers12092672
_version_ 1783596015958360064
author Chakladar, Jaideep
Kuo, Selena Z.
Castaneda, Grant
Li, Wei Tse
Gnanasekar, Aditi
Yu, Michael Andrew
Chang, Eric Y.
Wang, Xiao Qi
Ongkeko, Weg M.
author_facet Chakladar, Jaideep
Kuo, Selena Z.
Castaneda, Grant
Li, Wei Tse
Gnanasekar, Aditi
Yu, Michael Andrew
Chang, Eric Y.
Wang, Xiao Qi
Ongkeko, Weg M.
author_sort Chakladar, Jaideep
collection PubMed
description SIMPLE SUMMARY: The cancer microbiome has been suggested to be closely involved in the immune dysregulation that leads to carcinogenesis. Given that pancreatic adenocarcinoma (PAAD) is one of the most lethal cancers, it is important to identify features of the microbiome that may contribute to more deadly PAAD tumors. In this study, we analyzed PAAD patient RNA-sequencing data from The Cancer Genome Atlas (TCGA) to correlate abundance of intra-pancreatic microbes to dysregulation of immune and cancer-associated genes and pathways. We discovered that the presence of several bacteria species within PAAD tumors is linked to metastasis and immune suppression. Furthermore, we found that the increased prevalence and poorer prognosis of PAAD in males and smokers are linked to the presence of potentially cancer-promoting or immune-inhibiting microbes. Further study into the roles of these microbes in PAAD is imperative for understanding how a pro-tumor microenvironment may be treated to limit cancer progression. ABSTRACT: An intra-pancreatic microbiota was recently discovered in several prominent studies. Since pancreatic adenocarcinoma (PAAD) is one of the most lethal cancers worldwide, and the intratumor microbiome was found to be a significant contributor to carcinogenesis in other cancers, this study aims to characterize the PAAD microbiome and elucidate how it may be associated with PAAD prognosis. We further explored the association between the intra-pancreatic microbiome and smoking and gender, which are both risk factors for PAAD. RNA-sequencing data from The Cancer Genome Atlas (TCGA) were used to infer microbial abundance, which was correlated to clinical variables and to cancer and immune-associated gene expression, to determine how microbes may contribute to cancer progression. We discovered that the presence of several bacteria species within PAAD tumors is linked to metastasis and immune suppression. This is the first large-scale study to report microbiome-immune correlations in human pancreatic cancer samples. Furthermore, we found that the increased prevalence and poorer prognosis of PAAD in males and smokers are linked to the presence of potentially cancer-promoting or immune-inhibiting microbes. Further study into the roles of these microbes in PAAD is imperative for understanding how a pro-tumor microenvironment may be treated to limit cancer progression.
format Online
Article
Text
id pubmed-7565819
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-75658192020-10-26 The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers Chakladar, Jaideep Kuo, Selena Z. Castaneda, Grant Li, Wei Tse Gnanasekar, Aditi Yu, Michael Andrew Chang, Eric Y. Wang, Xiao Qi Ongkeko, Weg M. Cancers (Basel) Article SIMPLE SUMMARY: The cancer microbiome has been suggested to be closely involved in the immune dysregulation that leads to carcinogenesis. Given that pancreatic adenocarcinoma (PAAD) is one of the most lethal cancers, it is important to identify features of the microbiome that may contribute to more deadly PAAD tumors. In this study, we analyzed PAAD patient RNA-sequencing data from The Cancer Genome Atlas (TCGA) to correlate abundance of intra-pancreatic microbes to dysregulation of immune and cancer-associated genes and pathways. We discovered that the presence of several bacteria species within PAAD tumors is linked to metastasis and immune suppression. Furthermore, we found that the increased prevalence and poorer prognosis of PAAD in males and smokers are linked to the presence of potentially cancer-promoting or immune-inhibiting microbes. Further study into the roles of these microbes in PAAD is imperative for understanding how a pro-tumor microenvironment may be treated to limit cancer progression. ABSTRACT: An intra-pancreatic microbiota was recently discovered in several prominent studies. Since pancreatic adenocarcinoma (PAAD) is one of the most lethal cancers worldwide, and the intratumor microbiome was found to be a significant contributor to carcinogenesis in other cancers, this study aims to characterize the PAAD microbiome and elucidate how it may be associated with PAAD prognosis. We further explored the association between the intra-pancreatic microbiome and smoking and gender, which are both risk factors for PAAD. RNA-sequencing data from The Cancer Genome Atlas (TCGA) were used to infer microbial abundance, which was correlated to clinical variables and to cancer and immune-associated gene expression, to determine how microbes may contribute to cancer progression. We discovered that the presence of several bacteria species within PAAD tumors is linked to metastasis and immune suppression. This is the first large-scale study to report microbiome-immune correlations in human pancreatic cancer samples. Furthermore, we found that the increased prevalence and poorer prognosis of PAAD in males and smokers are linked to the presence of potentially cancer-promoting or immune-inhibiting microbes. Further study into the roles of these microbes in PAAD is imperative for understanding how a pro-tumor microenvironment may be treated to limit cancer progression. MDPI 2020-09-18 /pmc/articles/PMC7565819/ /pubmed/32962112 http://dx.doi.org/10.3390/cancers12092672 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chakladar, Jaideep
Kuo, Selena Z.
Castaneda, Grant
Li, Wei Tse
Gnanasekar, Aditi
Yu, Michael Andrew
Chang, Eric Y.
Wang, Xiao Qi
Ongkeko, Weg M.
The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title_full The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title_fullStr The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title_full_unstemmed The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title_short The Pancreatic Microbiome is Associated with Carcinogenesis and Worse Prognosis in Males and Smokers
title_sort pancreatic microbiome is associated with carcinogenesis and worse prognosis in males and smokers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7565819/
https://www.ncbi.nlm.nih.gov/pubmed/32962112
http://dx.doi.org/10.3390/cancers12092672
work_keys_str_mv AT chakladarjaideep thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT kuoselenaz thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT castanedagrant thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT liweitse thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT gnanasekaraditi thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT yumichaelandrew thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT changericy thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT wangxiaoqi thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT ongkekowegm thepancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT chakladarjaideep pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT kuoselenaz pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT castanedagrant pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT liweitse pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT gnanasekaraditi pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT yumichaelandrew pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT changericy pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT wangxiaoqi pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers
AT ongkekowegm pancreaticmicrobiomeisassociatedwithcarcinogenesisandworseprognosisinmalesandsmokers