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KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion
Mutations in the KRAS gene and overexpression of protein products of the MYC and ARF6 genes occur frequently in cancer. Here, the inseparable relationships and cooperation of the protein products of these three genes in cancer malignancy and immune evasion are discussed. mRNAs encoded by these genes...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165578/ https://www.ncbi.nlm.nih.gov/pubmed/37158894 http://dx.doi.org/10.1186/s12964-023-01130-3 |
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author | Sabe, Hisataka |
author_facet | Sabe, Hisataka |
author_sort | Sabe, Hisataka |
collection | PubMed |
description | Mutations in the KRAS gene and overexpression of protein products of the MYC and ARF6 genes occur frequently in cancer. Here, the inseparable relationships and cooperation of the protein products of these three genes in cancer malignancy and immune evasion are discussed. mRNAs encoded by these genes share the common feature of a G-quadruplex structure, which directs them to be robustly expressed when cellular energy production is increased. These three proteins are also functionally inseparable from each other, as follows. 1) KRAS induces MYC gene expression, and may also promote eIF4A-dependent MYC and ARF6 mRNA translation, 2) MYC induces the expression of genes involved in mitochondrial biogenesis and oxidative phosphorylation, and 3) ARF6 protects mitochondria from oxidative injury. ARF6 may moreover promote cancer invasion and metastasis, and also acidosis and immune checkpoint. Therefore, the inseparable relationships and cooperation of KRAS, MYC, and ARF6 appear to result in the activation of mitochondria and the driving of ARF6-based malignancy and immune evasion. Such adverse associations are frequent in pancreatic cancer, and appear to be further enhanced by TP53 mutations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01130-3. |
format | Online Article Text |
id | pubmed-10165578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101655782023-05-09 KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion Sabe, Hisataka Cell Commun Signal Review Mutations in the KRAS gene and overexpression of protein products of the MYC and ARF6 genes occur frequently in cancer. Here, the inseparable relationships and cooperation of the protein products of these three genes in cancer malignancy and immune evasion are discussed. mRNAs encoded by these genes share the common feature of a G-quadruplex structure, which directs them to be robustly expressed when cellular energy production is increased. These three proteins are also functionally inseparable from each other, as follows. 1) KRAS induces MYC gene expression, and may also promote eIF4A-dependent MYC and ARF6 mRNA translation, 2) MYC induces the expression of genes involved in mitochondrial biogenesis and oxidative phosphorylation, and 3) ARF6 protects mitochondria from oxidative injury. ARF6 may moreover promote cancer invasion and metastasis, and also acidosis and immune checkpoint. Therefore, the inseparable relationships and cooperation of KRAS, MYC, and ARF6 appear to result in the activation of mitochondria and the driving of ARF6-based malignancy and immune evasion. Such adverse associations are frequent in pancreatic cancer, and appear to be further enhanced by TP53 mutations. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-023-01130-3. BioMed Central 2023-05-08 /pmc/articles/PMC10165578/ /pubmed/37158894 http://dx.doi.org/10.1186/s12964-023-01130-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Sabe, Hisataka KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title | KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title_full | KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title_fullStr | KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title_full_unstemmed | KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title_short | KRAS, MYC, and ARF6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
title_sort | kras, myc, and arf6: inseparable relationships cooperatively promote cancer malignancy and immune evasion |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10165578/ https://www.ncbi.nlm.nih.gov/pubmed/37158894 http://dx.doi.org/10.1186/s12964-023-01130-3 |
work_keys_str_mv | AT sabehisataka krasmycandarf6inseparablerelationshipscooperativelypromotecancermalignancyandimmuneevasion |