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High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma

Pancreatic cancer ranks one of the worst in overall survival outcome with a 5 year survival rate being less than 10%. Pancreatic cancer faces unique challenges in its diagnosis and treatment, such as the lack of clinically validated biomarkers and the immensely immunosuppressive tumor microenvironme...

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Autores principales: Russ, Eric, Bhuvaneshwar, Krithika, Wang, Guisong, Jin, Benjamin, Gage, Michele M., Madhavan, Subha, Gusev, Yuriy, Upadhyay, Geeta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869573/
https://www.ncbi.nlm.nih.gov/pubmed/33613843
http://dx.doi.org/10.18632/oncotarget.27880
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author Russ, Eric
Bhuvaneshwar, Krithika
Wang, Guisong
Jin, Benjamin
Gage, Michele M.
Madhavan, Subha
Gusev, Yuriy
Upadhyay, Geeta
author_facet Russ, Eric
Bhuvaneshwar, Krithika
Wang, Guisong
Jin, Benjamin
Gage, Michele M.
Madhavan, Subha
Gusev, Yuriy
Upadhyay, Geeta
author_sort Russ, Eric
collection PubMed
description Pancreatic cancer ranks one of the worst in overall survival outcome with a 5 year survival rate being less than 10%. Pancreatic cancer faces unique challenges in its diagnosis and treatment, such as the lack of clinically validated biomarkers and the immensely immunosuppressive tumor microenvironment. Recently, the LY6 gene family has received increasing attention for its multi-faceted roles in cancer development, stem cell maintenance, immunomodulation, and association with more aggressive and hard-to-treat cancers. A detailed study of mRNA expression of LY6 gene family and its association with overall survival (OS) outcome in pancreatic cancers is lacking. We used publicly available clinical datasets to analyze the mRNA expression of a set of LY6 genes and its effect on OS outcome in the context of the tumor microenvironment and immunomodulation. We used web-based tools Kaplan-Meier Plotter, cBioPortal, Oncomine and R-programming to analyze copy number alterations, mRNA expression and its association with OS outcome in pancreatic cancer. These analyses demonstrated that high expression of LY6 genes is associated with OS and disease free survival (DFS) outcome. High expression of LY6 genes and their association with OS outcome is dependent on the composition of tumor microenvironment. Considering that LY6 proteins are anchored to the outer cell membrane or secreted, making them readily accessible, these findings highlight the potential of LY6 family members in the future of pancreatic cancer diagnosis and treatment.
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spelling pubmed-78695732021-02-18 High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma Russ, Eric Bhuvaneshwar, Krithika Wang, Guisong Jin, Benjamin Gage, Michele M. Madhavan, Subha Gusev, Yuriy Upadhyay, Geeta Oncotarget Research Paper Pancreatic cancer ranks one of the worst in overall survival outcome with a 5 year survival rate being less than 10%. Pancreatic cancer faces unique challenges in its diagnosis and treatment, such as the lack of clinically validated biomarkers and the immensely immunosuppressive tumor microenvironment. Recently, the LY6 gene family has received increasing attention for its multi-faceted roles in cancer development, stem cell maintenance, immunomodulation, and association with more aggressive and hard-to-treat cancers. A detailed study of mRNA expression of LY6 gene family and its association with overall survival (OS) outcome in pancreatic cancers is lacking. We used publicly available clinical datasets to analyze the mRNA expression of a set of LY6 genes and its effect on OS outcome in the context of the tumor microenvironment and immunomodulation. We used web-based tools Kaplan-Meier Plotter, cBioPortal, Oncomine and R-programming to analyze copy number alterations, mRNA expression and its association with OS outcome in pancreatic cancer. These analyses demonstrated that high expression of LY6 genes is associated with OS and disease free survival (DFS) outcome. High expression of LY6 genes and their association with OS outcome is dependent on the composition of tumor microenvironment. Considering that LY6 proteins are anchored to the outer cell membrane or secreted, making them readily accessible, these findings highlight the potential of LY6 family members in the future of pancreatic cancer diagnosis and treatment. Impact Journals LLC 2021-02-02 /pmc/articles/PMC7869573/ /pubmed/33613843 http://dx.doi.org/10.18632/oncotarget.27880 Text en Copyright: © 2021 Russ et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Russ, Eric
Bhuvaneshwar, Krithika
Wang, Guisong
Jin, Benjamin
Gage, Michele M.
Madhavan, Subha
Gusev, Yuriy
Upadhyay, Geeta
High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title_full High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title_fullStr High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title_full_unstemmed High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title_short High mRNA expression of LY6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
title_sort high mrna expression of ly6 gene family is associated with overall survival outcome in pancreatic ductal adenocarcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7869573/
https://www.ncbi.nlm.nih.gov/pubmed/33613843
http://dx.doi.org/10.18632/oncotarget.27880
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