IGF2BP1—An Oncofetal RNA-Binding Protein Fuels Tumor Virus Propagation
The oncofetal RNA-binding protein IGF2BP1 has been reported to be a driver of tumor progression in a multitude of cancer entities. Its main function is the stabilization of target transcripts by shielding these from miRNA-mediated degradation. However, there is growing evidence that several virus sp...
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| Published in | Viruses Vol. 15; no. 7; p. 1431 |
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| Main Authors | , |
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| Language | English |
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| Abstract | The oncofetal RNA-binding protein IGF2BP1 has been reported to be a driver of tumor progression in a multitude of cancer entities. Its main function is the stabilization of target transcripts by shielding these from miRNA-mediated degradation. However, there is growing evidence that several virus species recruit IGF2BP1 to promote their propagation. In particular, tumor-promoting viruses, such as hepatitis B/C and human papillomaviruses, benefit from IGF2BP1. Moreover, recent evidence suggests that non-oncogenic viruses, such as SARS-CoV-2, also take advantage of IGF2BP1. The only virus inhibited by IGF2BP1 reported to date is HIV-1. This review summarizes the current knowledge about the interactions between IGF2BP1 and different virus species. It further recapitulates several findings by presenting analyses from publicly available high-throughput datasets. |
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| AbstractList | The oncofetal RNA-binding protein IGF2BP1 has been reported to be a driver of tumor progression in a multitude of cancer entities. Its main function is the stabilization of target transcripts by shielding these from miRNA-mediated degradation. However, there is growing evidence that several virus species recruit IGF2BP1 to promote their propagation. In particular, tumor-promoting viruses, such as hepatitis B/C and human papillomaviruses, benefit from IGF2BP1. Moreover, recent evidence suggests that non-oncogenic viruses, such as SARS-CoV-2, also take advantage of IGF2BP1. The only virus inhibited by IGF2BP1 reported to date is HIV-1. This review summarizes the current knowledge about the interactions between IGF2BP1 and different virus species. It further recapitulates several findings by presenting analyses from publicly available high-throughput datasets. The oncofetal RNA-binding protein IGF2BP1 has been reported to be a driver of tumor progression in a multitude of cancer entities. Its main function is the stabilization of target transcripts by shielding these from miRNA-mediated degradation. However, there is growing evidence that several virus species recruit IGF2BP1 to promote their propagation. In particular, tumor-promoting viruses, such as hepatitis B/C and human papillomaviruses, benefit from IGF2BP1. Moreover, recent evidence suggests that non-oncogenic viruses, such as SARS-CoV-2, also take advantage of IGF2BP1. The only virus inhibited by IGF2BP1 reported to date is HIV-1. This review summarizes the current knowledge about the interactions between IGF2BP1 and different virus species. It further recapitulates several findings by presenting analyses from publicly available high-throughput datasets.The oncofetal RNA-binding protein IGF2BP1 has been reported to be a driver of tumor progression in a multitude of cancer entities. Its main function is the stabilization of target transcripts by shielding these from miRNA-mediated degradation. However, there is growing evidence that several virus species recruit IGF2BP1 to promote their propagation. In particular, tumor-promoting viruses, such as hepatitis B/C and human papillomaviruses, benefit from IGF2BP1. Moreover, recent evidence suggests that non-oncogenic viruses, such as SARS-CoV-2, also take advantage of IGF2BP1. The only virus inhibited by IGF2BP1 reported to date is HIV-1. This review summarizes the current knowledge about the interactions between IGF2BP1 and different virus species. It further recapitulates several findings by presenting analyses from publicly available high-throughput datasets. |
| Audience | Academic |
| Author | Hüttelmaier, Stefan Glaß, Markus |
| AuthorAffiliation | Institute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3a, 06120 Halle, Germany; stefan.huettelmaier@medizin.uni-halle.de |
| AuthorAffiliation_xml | – name: Institute of Molecular Medicine, Martin Luther University Halle-Wittenberg, Kurt-Mothes-Str. 3a, 06120 Halle, Germany; stefan.huettelmaier@medizin.uni-halle.de |
| Author_xml | – sequence: 1 givenname: Markus orcidid: 0000-0003-2718-8907 surname: Glaß fullname: Glaß, Markus – sequence: 2 givenname: Stefan orcidid: 0000-0001-9335-4227 surname: Hüttelmaier fullname: Hüttelmaier, Stefan |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37515119$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_cellsig_2025_111660 crossref_primary_10_1016_j_ejmech_2024_116241 crossref_primary_10_1002_mco2_70134 crossref_primary_10_1186_s10020_024_00936_2 |
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| Keywords | SARS-CoV-2 HIV IGF2BP1 HCV HBV virus HPV |
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| SubjectTerms | Binding proteins data collection HBV HCV Health aspects Hepatitis B Hepatitis C HIV HPV Human immunodeficiency virus Human papillomavirus IGF2BP1 Messenger RNA miRNA neoplasm progression neoplasms Oncogenic viruses Papillomaviridae Physiological aspects Review RNA viruses RNA-binding protein RNA-binding proteins Severe acute respiratory syndrome coronavirus 2 Tumor viruses Tumors Viral infections virus Virus research viruses Zika virus |
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| Title | IGF2BP1—An Oncofetal RNA-Binding Protein Fuels Tumor Virus Propagation |
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