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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...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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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. |
format | Online Article Text |
id | pubmed-8140388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
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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