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Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer

BACKGROUND/AIMS: The mineral-dust-induced gene mdig is a lung-cancer-associated oncogene. The focus of this study is to evaluate the expression status of mdig in lung cancer and to assess its influence in predicting the patient’s overall survival. METHODS: Using high-density tissue microarrays and c...

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Autores principales: Shi, Junwei, Thakur, Chitra, Zhao, Yuzu, Li, Yongsen, Nie, Lishen, Zhang, Qian, Bi, Zhuoyue, Fu, Yao, Wadgaonkar, Priya, Almutairy, Bandar, Xu, Liping, Zhang, Wenxuan, Qiu, Yiran, Rice, M’kya, Cui, Hongjuan, Chen, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140388/
https://www.ncbi.nlm.nih.gov/pubmed/33423409
http://dx.doi.org/10.33594/000000322
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author Shi, Junwei
Thakur, Chitra
Zhao, Yuzu
Li, Yongsen
Nie, Lishen
Zhang, Qian
Bi, Zhuoyue
Fu, Yao
Wadgaonkar, Priya
Almutairy, Bandar
Xu, Liping
Zhang, Wenxuan
Qiu, Yiran
Rice, M’kya
Cui, Hongjuan
Chen, Fei
author_facet Shi, Junwei
Thakur, Chitra
Zhao, Yuzu
Li, Yongsen
Nie, Lishen
Zhang, Qian
Bi, Zhuoyue
Fu, Yao
Wadgaonkar, Priya
Almutairy, Bandar
Xu, Liping
Zhang, Wenxuan
Qiu, Yiran
Rice, M’kya
Cui, Hongjuan
Chen, Fei
author_sort Shi, Junwei
collection PubMed
description BACKGROUND/AIMS: The mineral-dust-induced gene mdig is a lung-cancer-associated oncogene. The focus of this study is to evaluate the expression status of mdig in lung cancer and to assess its influence in predicting the patient’s overall survival. METHODS: Using high-density tissue microarrays and clinical samples of synchronous multiple primary lung cancer (SMPLC), we investigated the expression of mdig through immunohistochemistry and utilized the open-access lung cancer patient databases containing genomic and transcriptomic data from the UCSC Xena and TCGA web platforms to determine the prognostic values of mdig expression status among different subtypes of lung cancer. RESULTS: mdig is upregulated in smokers and in lung squamous cell carcinoma. High mdig expression predicted poor overall survival in lung squamous cell carcinoma and female smokers. Among tumor tissues from SMPLC patients, we not only unraveled the highest positive rate of mdig expression, but also revealed a unique cytoplasmic, rather than nuclear localization of mdig protein. Furthermore, by inspecting some pathological but not cancerous lung tissues, we believe that mdig is required for the transformation of non-cancerous lung cells to the fully-fledged cancer cells. CONCLUSION: These data suggested that mdig is involved in various stages of lung carcinogenesis, possibly through the epigenetic regulation on some critical cancer-associated genes, and increased mdig expression is an important prognostic factor for some types of lung cancer.
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spelling pubmed-81403882021-05-22 Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer Shi, Junwei Thakur, Chitra Zhao, Yuzu Li, Yongsen Nie, Lishen Zhang, Qian Bi, Zhuoyue Fu, Yao Wadgaonkar, Priya Almutairy, Bandar Xu, Liping Zhang, Wenxuan Qiu, Yiran Rice, M’kya Cui, Hongjuan Chen, Fei Cell Physiol Biochem Article BACKGROUND/AIMS: The mineral-dust-induced gene mdig is a lung-cancer-associated oncogene. The focus of this study is to evaluate the expression status of mdig in lung cancer and to assess its influence in predicting the patient’s overall survival. METHODS: Using high-density tissue microarrays and clinical samples of synchronous multiple primary lung cancer (SMPLC), we investigated the expression of mdig through immunohistochemistry and utilized the open-access lung cancer patient databases containing genomic and transcriptomic data from the UCSC Xena and TCGA web platforms to determine the prognostic values of mdig expression status among different subtypes of lung cancer. RESULTS: mdig is upregulated in smokers and in lung squamous cell carcinoma. High mdig expression predicted poor overall survival in lung squamous cell carcinoma and female smokers. Among tumor tissues from SMPLC patients, we not only unraveled the highest positive rate of mdig expression, but also revealed a unique cytoplasmic, rather than nuclear localization of mdig protein. Furthermore, by inspecting some pathological but not cancerous lung tissues, we believe that mdig is required for the transformation of non-cancerous lung cells to the fully-fledged cancer cells. CONCLUSION: These data suggested that mdig is involved in various stages of lung carcinogenesis, possibly through the epigenetic regulation on some critical cancer-associated genes, and increased mdig expression is an important prognostic factor for some types of lung cancer. 2021-01-11 /pmc/articles/PMC8140388/ /pubmed/33423409 http://dx.doi.org/10.33594/000000322 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND). Usage and distribution for commercial purposes as well as any distribution of modified material requires written permission.
spellingShingle Article
Shi, Junwei
Thakur, Chitra
Zhao, Yuzu
Li, Yongsen
Nie, Lishen
Zhang, Qian
Bi, Zhuoyue
Fu, Yao
Wadgaonkar, Priya
Almutairy, Bandar
Xu, Liping
Zhang, Wenxuan
Qiu, Yiran
Rice, M’kya
Cui, Hongjuan
Chen, Fei
Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title_full Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title_fullStr Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title_full_unstemmed Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title_short Pathological and Prognostic Indications of the mdig Gene in Human Lung Cancer
title_sort pathological and prognostic indications of the mdig gene in human lung cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140388/
https://www.ncbi.nlm.nih.gov/pubmed/33423409
http://dx.doi.org/10.33594/000000322
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