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PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer

As a member of protein tyrosine phosphatases (PTPs), the protein tyrosine phosphatase receptor type O (PTPRO) has attracted increasing attention for its important roles in cell signaling. Currently, the roles of PTPRO in human cancers remain elusive. Herein, we performed bioinformatic analyses and r...

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Detalles Bibliográficos
Autores principales: Hou, Xuben, Du, Jintong, Fang, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734421/
https://www.ncbi.nlm.nih.gov/pubmed/35003364
http://dx.doi.org/10.7150/jca.64661
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author Hou, Xuben
Du, Jintong
Fang, Hao
author_facet Hou, Xuben
Du, Jintong
Fang, Hao
author_sort Hou, Xuben
collection PubMed
description As a member of protein tyrosine phosphatases (PTPs), the protein tyrosine phosphatase receptor type O (PTPRO) has attracted increasing attention for its important roles in cell signaling. Currently, the roles of PTPRO in human cancers remain elusive. Herein, we performed bioinformatic analyses and revealed the potential oncogenic role of PTPRO in specific cancer types. Further in vitro experiments indicated that inhibition of PTPRO suppresses the proliferative abilities of tumor cells in pancreatic cancer, blood cancer, and breast cancer. Moreover, small molecular PTPRO inhibitor could induce cell apoptosis and affect the cell cycle in pancreatic cancer. In addition, PTPRO expression promoted the infiltration of CD8+ T, macrophages, dendritic cells, and neutrophils, in pancreatic cancers. Our findings suggested PTPRO may serve as a potential drug target for pancreatic cancer.
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spelling pubmed-87344212022-01-06 PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer Hou, Xuben Du, Jintong Fang, Hao J Cancer Research Paper As a member of protein tyrosine phosphatases (PTPs), the protein tyrosine phosphatase receptor type O (PTPRO) has attracted increasing attention for its important roles in cell signaling. Currently, the roles of PTPRO in human cancers remain elusive. Herein, we performed bioinformatic analyses and revealed the potential oncogenic role of PTPRO in specific cancer types. Further in vitro experiments indicated that inhibition of PTPRO suppresses the proliferative abilities of tumor cells in pancreatic cancer, blood cancer, and breast cancer. Moreover, small molecular PTPRO inhibitor could induce cell apoptosis and affect the cell cycle in pancreatic cancer. In addition, PTPRO expression promoted the infiltration of CD8+ T, macrophages, dendritic cells, and neutrophils, in pancreatic cancers. Our findings suggested PTPRO may serve as a potential drug target for pancreatic cancer. Ivyspring International Publisher 2021-10-30 /pmc/articles/PMC8734421/ /pubmed/35003364 http://dx.doi.org/10.7150/jca.64661 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Hou, Xuben
Du, Jintong
Fang, Hao
PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title_full PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title_fullStr PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title_full_unstemmed PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title_short PTPRO is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
title_sort ptpro is a therapeutic target and correlated with immune infiltrates in pancreatic cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734421/
https://www.ncbi.nlm.nih.gov/pubmed/35003364
http://dx.doi.org/10.7150/jca.64661
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