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ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer
The human AlkB homolog family (ALKBH) of proteins play a critical role in some types of cancer. However, the expression and function of the lysine demethylase ALKBH4 in cancer are poorly understood. Here, we examined the expression and function of ALKBH4 in non-small-cell lung cancer (NSCLC) and fou...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060266/ https://www.ncbi.nlm.nih.gov/pubmed/33883577 http://dx.doi.org/10.1038/s41598-021-87763-1 |
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author | Jingushi, Kentaro Aoki, Masaya Ueda, Kazuhiro Kogaki, Takahiro Tanimoto, Masaya Monoe, Yuya Ando, Masayuki Matsumoto, Takuya Minami, Kentaro Ueda, Yuko Kitae, Kaori Hase, Hiroaki Nagata, Toshiyuki Harada-Takeda, Aya Yamamoto, Masatatsu Kawahara, Kohichi Tabata, Kazuhiro Furukawa, Tatsuhiko Sato, Masami Tsujikawa, Kazutake |
author_facet | Jingushi, Kentaro Aoki, Masaya Ueda, Kazuhiro Kogaki, Takahiro Tanimoto, Masaya Monoe, Yuya Ando, Masayuki Matsumoto, Takuya Minami, Kentaro Ueda, Yuko Kitae, Kaori Hase, Hiroaki Nagata, Toshiyuki Harada-Takeda, Aya Yamamoto, Masatatsu Kawahara, Kohichi Tabata, Kazuhiro Furukawa, Tatsuhiko Sato, Masami Tsujikawa, Kazutake |
author_sort | Jingushi, Kentaro |
collection | PubMed |
description | The human AlkB homolog family (ALKBH) of proteins play a critical role in some types of cancer. However, the expression and function of the lysine demethylase ALKBH4 in cancer are poorly understood. Here, we examined the expression and function of ALKBH4 in non-small-cell lung cancer (NSCLC) and found that ALKBH4 was highly expressed in NSCLC, as compared to that in adjacent normal lung tissues. ALKBH4 knockdown significantly induced the downregulation of NSCLC cell proliferation via cell cycle arrest at the G(1) phase of in vivo tumour growth. ALKBH4 knockdown downregulated E2F transcription factor 1 (E2F1) and its target gene expression in NSCLC cells. ALKBH4 and E2F1 expression was significantly correlated in NSCLC clinical specimens. Moreover, patients with high ALKBH4 expression showed a poor prognosis, suggesting that ALKBH4 plays a pivotal tumour-promoting role in NSCLC. |
format | Online Article Text |
id | pubmed-8060266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80602662021-04-22 ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer Jingushi, Kentaro Aoki, Masaya Ueda, Kazuhiro Kogaki, Takahiro Tanimoto, Masaya Monoe, Yuya Ando, Masayuki Matsumoto, Takuya Minami, Kentaro Ueda, Yuko Kitae, Kaori Hase, Hiroaki Nagata, Toshiyuki Harada-Takeda, Aya Yamamoto, Masatatsu Kawahara, Kohichi Tabata, Kazuhiro Furukawa, Tatsuhiko Sato, Masami Tsujikawa, Kazutake Sci Rep Article The human AlkB homolog family (ALKBH) of proteins play a critical role in some types of cancer. However, the expression and function of the lysine demethylase ALKBH4 in cancer are poorly understood. Here, we examined the expression and function of ALKBH4 in non-small-cell lung cancer (NSCLC) and found that ALKBH4 was highly expressed in NSCLC, as compared to that in adjacent normal lung tissues. ALKBH4 knockdown significantly induced the downregulation of NSCLC cell proliferation via cell cycle arrest at the G(1) phase of in vivo tumour growth. ALKBH4 knockdown downregulated E2F transcription factor 1 (E2F1) and its target gene expression in NSCLC cells. ALKBH4 and E2F1 expression was significantly correlated in NSCLC clinical specimens. Moreover, patients with high ALKBH4 expression showed a poor prognosis, suggesting that ALKBH4 plays a pivotal tumour-promoting role in NSCLC. Nature Publishing Group UK 2021-04-21 /pmc/articles/PMC8060266/ /pubmed/33883577 http://dx.doi.org/10.1038/s41598-021-87763-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jingushi, Kentaro Aoki, Masaya Ueda, Kazuhiro Kogaki, Takahiro Tanimoto, Masaya Monoe, Yuya Ando, Masayuki Matsumoto, Takuya Minami, Kentaro Ueda, Yuko Kitae, Kaori Hase, Hiroaki Nagata, Toshiyuki Harada-Takeda, Aya Yamamoto, Masatatsu Kawahara, Kohichi Tabata, Kazuhiro Furukawa, Tatsuhiko Sato, Masami Tsujikawa, Kazutake ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title | ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title_full | ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title_fullStr | ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title_full_unstemmed | ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title_short | ALKBH4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
title_sort | alkbh4 promotes tumourigenesis with a poor prognosis in non-small-cell lung cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060266/ https://www.ncbi.nlm.nih.gov/pubmed/33883577 http://dx.doi.org/10.1038/s41598-021-87763-1 |
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