Nuclear localization and actions of the insulin-like growth factor 1 (IGF-1) system components: Transcriptional regulation and DNA damage response
Authors:
- Elżbieta Poręba,
- Julia Łucja Durzyńska
Abstract
Insulin-like growth factor (IGF) system stimulates growth, proliferation, and regulates differentiation of cells in a tissue-specific manner. It is composed of two insulin-like growth factors (IGF-1 and IGF-2), six insulin-like growth factor-binding proteins (IGFBPs), and two insulin-like growth factor receptors (IGF-1R and IGF-2R). IGF actions take place mostly through the activation of the plasma membrane-bound IGF-Rs by the circulating ligands (IGFs) released from the IGFBPs that stabilize their levels in the serum. This review focuses on the IGF-1 part of the system. The IGF-1 gene, which is expressed mainly in the liver as well as in other tissues, comprises six alternatively spliced exons that code for three protein isoforms (pro-IGF-1A, pro-IGF-1B, and pro-IGF-1C), which are processed to mature IGF-1 and E-peptides. The IGF-1R undergoes autophosphorylation, resulting in a signaling cascade involving numerous cytoplasmic proteins such as AKT and MAPKs, which regulate the expression of target genes. However, a more complex picture of the axis has recently emerged with all its components being translocated to the nuclear compartment. IGF-1R takes part in the regulation of gene expression by forming transcription complexes, modifying the activity of chromatin remodeling proteins, and participating in DNA damage tolerance mechanisms. Four IGFBPs contain a nuclear localization signal (NLS), which targets them to the nucleus, where they regulate gene expression (IGFBP-2, IGFBP-3, IGFBP-5, IGFBP-6) and DNA damage repair (IGFBP-3 and IGFBP-6). Last but not least, the IGF-1B isoform has been reported to be localized in the nuclear compartment. However, no specific molecular actions have been assigned to the nuclear pro-IGF-1B or its derivative EB peptide. Therefore, further studies are needed to shed light on their nuclear activity. These recently uncovered nuclear actions of different components of the IGF-1 axis are relevant in cancer cell biology and are discussed in this review. © 2020 The Authors
- Record ID
- UAM0b718244ad6049a6ae876f1cfa0b4bcd
- Author
- Journal series
- Mutation Research-Reviews in Mutation Research, ISSN 1383-5742, e-ISSN 1388-2139
- Issue year
- 2020
- Vol
- 784
- Pages
- 1-19
- Keywords in English
- Cancer cell biology; DNA damage response; IGF-1 system; Nuclear localization; Transcriptional regulation; insulin like growth factor 1A; insulin like growth factor 1B; insulin like growth factor 1C; isoprotein; mitogen activated protein kinase; peptide E; protein kinase B; somatomedin binding protein 1; somatomedin binding protein 2; somatomedin binding protein 3; somatomedin binding protein 5; somatomedin binding protein 6; somatomedin C; unclassified drug, autophosphorylation; chromatin assembly and disassembly; DNA damage response; exon; gene expression regulation; human; nonhuman; nuclear import; nuclear localization signal; priority journal; protein function; protein localization; Review; transcription regulation
- ASJC Classification
- ;
- DOI
- DOI:10.1016/j.mrrev.2020.108307 Opening in a new tab
- URL
- https://www.scopus.com/inward/record.uri?eid=2-s2.0-85081034760&doi=10.1016%2fj.mrrev.2020.108307&partnerID=40&md5=eb501b361f1e1b2bfc3b3d4ed7753fcf Opening in a new tab
- Language
- (en) English
- Score (nominal)
- 100
- Score source
- journalList
- Score
- = 100.0, 14-05-2022, ArticleFromJournal
- Publication indicators
- = 11; = 5; = 9; : 2017 = 1.588; : 2019 (2 years) = 5.803 - 2019 (5 years) =6.041
- Citation count
- 13
- Uniform Resource Identifier
- https://researchportal.amu.edu.pl/info/article/UAM0b718244ad6049a6ae876f1cfa0b4bcd/
- URN
urn:amu-prod:UAM0b718244ad6049a6ae876f1cfa0b4bcd
* presented citation count is obtained through Internet information analysis and it is close to the number calculated by the Publish or PerishOpening in a new tab system.