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The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines

PURPOSE: Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) is a tetramethylfolate dehydrogenase enzyme involved in folate metabolism. The aim of this study is to determine the effect of MTHFD2 on the proliferation and metastasis of colorectal cancer (CRC). PATIENTS AND METHODS: MTHFD2 was silenced...

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Autores principales: Wei, Yameng, Liu, Pengfei, Li, Qian, Du, Juan, Chen, Yani, Wang, Yu, Shi, Haiyan, Wang, Yanfeng, Zhang, Huahua, Xue, Wanjuan, Gao, Yi, Li, Dan, Feng, Yun, Yan, Jing, Han, Jiming, Zhang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697661/
https://www.ncbi.nlm.nih.gov/pubmed/31496738
http://dx.doi.org/10.2147/OTT.S210800
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author Wei, Yameng
Liu, Pengfei
Li, Qian
Du, Juan
Chen, Yani
Wang, Yu
Shi, Haiyan
Wang, Yanfeng
Zhang, Huahua
Xue, Wanjuan
Gao, Yi
Li, Dan
Feng, Yun
Yan, Jing
Han, Jiming
Zhang, Jing
author_facet Wei, Yameng
Liu, Pengfei
Li, Qian
Du, Juan
Chen, Yani
Wang, Yu
Shi, Haiyan
Wang, Yanfeng
Zhang, Huahua
Xue, Wanjuan
Gao, Yi
Li, Dan
Feng, Yun
Yan, Jing
Han, Jiming
Zhang, Jing
author_sort Wei, Yameng
collection PubMed
description PURPOSE: Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) is a tetramethylfolate dehydrogenase enzyme involved in folate metabolism. The aim of this study is to determine the effect of MTHFD2 on the proliferation and metastasis of colorectal cancer (CRC). PATIENTS AND METHODS: MTHFD2 was silenced or overexpressed in CRC cells. qRT-PCR and Western blotting were used to analyze mRNA and protein expression, respectively. The MTT assay and colony forming assay were used to detect cell proliferation and colony formation ability. The cycle and apoptosis changes were detected by flow cytometry. Transwell experiments were used to analyze the migration ability of CRC cells. RESULTS: The expression of MTHFD2 in 31 kinds of cancers was analyzed by bioinformatics, and MTHFD2 was found highly expressed in various cancer cells including CRC cells. Silencing the expression of MTHFD2 resulted in inhibition of the proliferation of CRC cells, weakening of the migration ability, blocking of the cell cycle in G0/G1-S phase, and promotion of the apoptosis of CRC cells. On the contrary, overexpression of MTHFD2 in CRC cells resulted in enhancement of the proliferation and migration ability, promotion of cell cycle progression and inhibition of cell apoptosis. CONCLUSION: MTHFD2 is positively related with colorectal cancer and the MTHFD2 gene is a tumor promoting gene in CRC cells.
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spelling pubmed-66976612019-09-06 The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines Wei, Yameng Liu, Pengfei Li, Qian Du, Juan Chen, Yani Wang, Yu Shi, Haiyan Wang, Yanfeng Zhang, Huahua Xue, Wanjuan Gao, Yi Li, Dan Feng, Yun Yan, Jing Han, Jiming Zhang, Jing Onco Targets Ther Original Research PURPOSE: Methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) is a tetramethylfolate dehydrogenase enzyme involved in folate metabolism. The aim of this study is to determine the effect of MTHFD2 on the proliferation and metastasis of colorectal cancer (CRC). PATIENTS AND METHODS: MTHFD2 was silenced or overexpressed in CRC cells. qRT-PCR and Western blotting were used to analyze mRNA and protein expression, respectively. The MTT assay and colony forming assay were used to detect cell proliferation and colony formation ability. The cycle and apoptosis changes were detected by flow cytometry. Transwell experiments were used to analyze the migration ability of CRC cells. RESULTS: The expression of MTHFD2 in 31 kinds of cancers was analyzed by bioinformatics, and MTHFD2 was found highly expressed in various cancer cells including CRC cells. Silencing the expression of MTHFD2 resulted in inhibition of the proliferation of CRC cells, weakening of the migration ability, blocking of the cell cycle in G0/G1-S phase, and promotion of the apoptosis of CRC cells. On the contrary, overexpression of MTHFD2 in CRC cells resulted in enhancement of the proliferation and migration ability, promotion of cell cycle progression and inhibition of cell apoptosis. CONCLUSION: MTHFD2 is positively related with colorectal cancer and the MTHFD2 gene is a tumor promoting gene in CRC cells. Dove 2019-08-12 /pmc/articles/PMC6697661/ /pubmed/31496738 http://dx.doi.org/10.2147/OTT.S210800 Text en © 2019 Wei 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
Wei, Yameng
Liu, Pengfei
Li, Qian
Du, Juan
Chen, Yani
Wang, Yu
Shi, Haiyan
Wang, Yanfeng
Zhang, Huahua
Xue, Wanjuan
Gao, Yi
Li, Dan
Feng, Yun
Yan, Jing
Han, Jiming
Zhang, Jing
The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title_full The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title_fullStr The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title_full_unstemmed The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title_short The effect of MTHFD2 on the proliferation and migration of colorectal cancer cell lines
title_sort effect of mthfd2 on the proliferation and migration of colorectal cancer cell lines
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6697661/
https://www.ncbi.nlm.nih.gov/pubmed/31496738
http://dx.doi.org/10.2147/OTT.S210800
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