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Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2

As a cellular protease, transmembrane serine protease 2 (TMPRSS2) plays roles in various physiological and pathological processes, including cancer and viral entry, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Herein, we conducted expression, mutation, and prognostic analyse...

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Autores principales: Fu, Jiewen, Liu, Shuguang, Tan, Qi, Liu, Zhiying, Qian, Jie, Li, Ting, Du, Jiaman, Song, Binghui, Li, Dabing, Zhang, Lianmei, He, Jiayue, Guo, Kan, Zhou, Baixu, Chen, Hanchun, Fu, Shangyi, Liu, Xiaoyan, Cheng, Jingliang, He, Tao, Fu, Junjiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658242/
https://www.ncbi.nlm.nih.gov/pubmed/36364238
http://dx.doi.org/10.3390/molecules27217413
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author Fu, Jiewen
Liu, Shuguang
Tan, Qi
Liu, Zhiying
Qian, Jie
Li, Ting
Du, Jiaman
Song, Binghui
Li, Dabing
Zhang, Lianmei
He, Jiayue
Guo, Kan
Zhou, Baixu
Chen, Hanchun
Fu, Shangyi
Liu, Xiaoyan
Cheng, Jingliang
He, Tao
Fu, Junjiang
author_facet Fu, Jiewen
Liu, Shuguang
Tan, Qi
Liu, Zhiying
Qian, Jie
Li, Ting
Du, Jiaman
Song, Binghui
Li, Dabing
Zhang, Lianmei
He, Jiayue
Guo, Kan
Zhou, Baixu
Chen, Hanchun
Fu, Shangyi
Liu, Xiaoyan
Cheng, Jingliang
He, Tao
Fu, Junjiang
author_sort Fu, Jiewen
collection PubMed
description As a cellular protease, transmembrane serine protease 2 (TMPRSS2) plays roles in various physiological and pathological processes, including cancer and viral entry, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Herein, we conducted expression, mutation, and prognostic analyses for the TMPRSS2 gene in pan-cancers as well as in COVID-19-infected lung tissues. The results indicate that TMPRSS2 expression was highest in prostate cancer. A high expression of TMPRSS2 was significantly associated with a short overall survival in breast invasive carcinoma (BRCA), sarcoma (SARC), and uveal melanoma (UVM), while a low expression of TMPRSS2 was significantly associated with a short overall survival in lung adenocarcinoma (LUAD), demonstrating TMPRSS2 roles in cancer patient susceptibility and severity. Additionally, TMPRSS2 expression in COVID-19-infected lung tissues was significantly reduced compared to healthy lung tissues, indicating that a low TMPRSS2 expression may result in COVID-19 severity and death. Importantly, TMPRSS2 mutation frequency was significantly higher in prostate adenocarcinoma (PRAD), and the mutant TMPRSS2 pan-cancer group was significantly associated with long overall, progression-free, disease-specific, and disease-free survival rates compared to the wild-type (WT) TMPRSS2 pan-cancer group, demonstrating loss of functional roles due to mutation. Cancer cell lines were treated with small molecules, including cordycepin (CD), adenosine (AD), thymoquinone (TQ), and TQFL12, to mediate TMPRSS2 expression. Notably, CD, AD, TQ, and TQFL12 inhibited TMPRSS2 expression in cancer cell lines, including the PC3 prostate cancer cell line, implying a therapeutic role for preventing COVID-19 in cancer patients. Together, these findings are the first to demonstrate that small molecules, such as CD, AD, TQ, and TQFL12, inhibit TMPRSS2 expression, providing novel therapeutic strategies for preventing COVID-19 and cancers.
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spelling pubmed-96582422022-11-15 Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2 Fu, Jiewen Liu, Shuguang Tan, Qi Liu, Zhiying Qian, Jie Li, Ting Du, Jiaman Song, Binghui Li, Dabing Zhang, Lianmei He, Jiayue Guo, Kan Zhou, Baixu Chen, Hanchun Fu, Shangyi Liu, Xiaoyan Cheng, Jingliang He, Tao Fu, Junjiang Molecules Article As a cellular protease, transmembrane serine protease 2 (TMPRSS2) plays roles in various physiological and pathological processes, including cancer and viral entry, such as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Herein, we conducted expression, mutation, and prognostic analyses for the TMPRSS2 gene in pan-cancers as well as in COVID-19-infected lung tissues. The results indicate that TMPRSS2 expression was highest in prostate cancer. A high expression of TMPRSS2 was significantly associated with a short overall survival in breast invasive carcinoma (BRCA), sarcoma (SARC), and uveal melanoma (UVM), while a low expression of TMPRSS2 was significantly associated with a short overall survival in lung adenocarcinoma (LUAD), demonstrating TMPRSS2 roles in cancer patient susceptibility and severity. Additionally, TMPRSS2 expression in COVID-19-infected lung tissues was significantly reduced compared to healthy lung tissues, indicating that a low TMPRSS2 expression may result in COVID-19 severity and death. Importantly, TMPRSS2 mutation frequency was significantly higher in prostate adenocarcinoma (PRAD), and the mutant TMPRSS2 pan-cancer group was significantly associated with long overall, progression-free, disease-specific, and disease-free survival rates compared to the wild-type (WT) TMPRSS2 pan-cancer group, demonstrating loss of functional roles due to mutation. Cancer cell lines were treated with small molecules, including cordycepin (CD), adenosine (AD), thymoquinone (TQ), and TQFL12, to mediate TMPRSS2 expression. Notably, CD, AD, TQ, and TQFL12 inhibited TMPRSS2 expression in cancer cell lines, including the PC3 prostate cancer cell line, implying a therapeutic role for preventing COVID-19 in cancer patients. Together, these findings are the first to demonstrate that small molecules, such as CD, AD, TQ, and TQFL12, inhibit TMPRSS2 expression, providing novel therapeutic strategies for preventing COVID-19 and cancers. MDPI 2022-11-01 /pmc/articles/PMC9658242/ /pubmed/36364238 http://dx.doi.org/10.3390/molecules27217413 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fu, Jiewen
Liu, Shuguang
Tan, Qi
Liu, Zhiying
Qian, Jie
Li, Ting
Du, Jiaman
Song, Binghui
Li, Dabing
Zhang, Lianmei
He, Jiayue
Guo, Kan
Zhou, Baixu
Chen, Hanchun
Fu, Shangyi
Liu, Xiaoyan
Cheng, Jingliang
He, Tao
Fu, Junjiang
Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title_full Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title_fullStr Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title_full_unstemmed Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title_short Impact of TMPRSS2 Expression, Mutation Prognostics, and Small Molecule (CD, AD, TQ, and TQFL12) Inhibition on Pan-Cancer Tumors and Susceptibility to SARS-CoV-2
title_sort impact of tmprss2 expression, mutation prognostics, and small molecule (cd, ad, tq, and tqfl12) inhibition on pan-cancer tumors and susceptibility to sars-cov-2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9658242/
https://www.ncbi.nlm.nih.gov/pubmed/36364238
http://dx.doi.org/10.3390/molecules27217413
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