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TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect
BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallma...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767749/ https://www.ncbi.nlm.nih.gov/pubmed/33380827 http://dx.doi.org/10.2147/CMAR.S287956 |
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author | Xing, Yutong Luo, Peng Hu, Rui Wang, Duanduan Zhou, Gang Jiang, Jie |
author_facet | Xing, Yutong Luo, Peng Hu, Rui Wang, Duanduan Zhou, Gang Jiang, Jie |
author_sort | Xing, Yutong |
collection | PubMed |
description | BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallmark of cancer. However, the exact role and molecular mechanism of TRIB3 in lung adenocarcinoma (LUAD) cell reprogramming is largely unknown. METHODS: The oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) of cells were examined with a Seahorse XF Extracellular Flux Analyzer. In vitro and in vivo RT-qPCR, Western blotting, and functional assays were performed to explore the functional roles of TRIB3 in LUAD. RESULTS: In the present study, we demonstrated that TRIB3 is remarkably upregulated in LUAD cell lines as well as tissues. TRIB3 knockdown significantly inhibited LUAD cell growth and suppressed LUAD cell invasion, while TRIB3 overexpression conferred the opposite effects. Moreover, silencing TRIB3 suppressed the tumorigenesis and metastatic ability of LUAD cells. Mechanistically, we demonstrated that silencing TRIB3 significantly impaired aerobic glycolysis ability in LUAD cells. Furthermore, our data indicated that TRIB3 knockdown decreased hypoxia-inducible factor (HIF)1α levels and targeted the glycolytic genes regulated by HIF1α. CONCLUSION: Together, our findings revealed a previously unappreciated function of TRIB3 in cancer cell metabolism and tumor progression, illustrating that TRIB3 could be considered a valuable therapeutic target for LUAD patients. |
format | Online Article Text |
id | pubmed-7767749 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-77677492020-12-29 TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect Xing, Yutong Luo, Peng Hu, Rui Wang, Duanduan Zhou, Gang Jiang, Jie Cancer Manag Res Original Research BACKGROUND: The pseudokinase Tribbles 3 (TRIB3) is involved in many cellular processes and various cancers. In recent years, the importance of metabolic transformation in the maintenance of malignant tumors has become increasingly prominent. Abnormal metabolism of cancer cells is considered a hallmark of cancer. However, the exact role and molecular mechanism of TRIB3 in lung adenocarcinoma (LUAD) cell reprogramming is largely unknown. METHODS: The oxygen consumption rate (OCR) and extracellular acidification rate (ECAR) of cells were examined with a Seahorse XF Extracellular Flux Analyzer. In vitro and in vivo RT-qPCR, Western blotting, and functional assays were performed to explore the functional roles of TRIB3 in LUAD. RESULTS: In the present study, we demonstrated that TRIB3 is remarkably upregulated in LUAD cell lines as well as tissues. TRIB3 knockdown significantly inhibited LUAD cell growth and suppressed LUAD cell invasion, while TRIB3 overexpression conferred the opposite effects. Moreover, silencing TRIB3 suppressed the tumorigenesis and metastatic ability of LUAD cells. Mechanistically, we demonstrated that silencing TRIB3 significantly impaired aerobic glycolysis ability in LUAD cells. Furthermore, our data indicated that TRIB3 knockdown decreased hypoxia-inducible factor (HIF)1α levels and targeted the glycolytic genes regulated by HIF1α. CONCLUSION: Together, our findings revealed a previously unappreciated function of TRIB3 in cancer cell metabolism and tumor progression, illustrating that TRIB3 could be considered a valuable therapeutic target for LUAD patients. Dove 2020-12-23 /pmc/articles/PMC7767749/ /pubmed/33380827 http://dx.doi.org/10.2147/CMAR.S287956 Text en © 2020 Xing et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Xing, Yutong Luo, Peng Hu, Rui Wang, Duanduan Zhou, Gang Jiang, Jie TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title | TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title_full | TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title_fullStr | TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title_full_unstemmed | TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title_short | TRIB3 Promotes Lung Adenocarcinoma Progression via an Enhanced Warburg Effect |
title_sort | trib3 promotes lung adenocarcinoma progression via an enhanced warburg effect |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767749/ https://www.ncbi.nlm.nih.gov/pubmed/33380827 http://dx.doi.org/10.2147/CMAR.S287956 |
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