Interleukin enhancer-binding factor 2 promotes cell proliferation and DNA damage response in metastatic melanoma.

Autor: Zhang X; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California., Bustos MA; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California., Gross R; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California., Ramos RI; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California., Takeshima TL; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California., Mills GB; Department of Cell Development and Cancer Biology, Knight Cancer Institute, Oregon Health and Science University, Portland, Oregon., Yu Q; Agency for Science Technology and Research (A*STAR), Genome Institute of Singapore, Biopolis, Singapore., Hoon DSB; Department of Translational Molecular Medicine, Providence Saint John's Health Center, Saint John's Cancer Institute, Santa Monica, California.
Jazyk: angličtina
Zdroj: Clinical and translational medicine [Clin Transl Med] 2021 Oct; Vol. 11 (10), pp. e608.
DOI: 10.1002/ctm2.608
Abstrakt: Background: 1q21.3 amplification, which is frequently observed in metastatic melanoma, is associated with cancer progression. Interleukin enhancer-binding factor 2 (ILF2) is located in the 1q21.3 amplified region, but its functional role or contribution to tumour aggressiveness in cutaneous melanoma is unknown.
Methods: In silico analyses were performed using the TCGA SKCM dataset with clinical annotations and three melanoma microarray cohorts from the GEO datasets. RNA in situ hybridisation and immunohistochemistry were utilised to validate the gene expression in melanoma tissues. Four stable melanoma cell lines were established for in vitro ILF2 functional characterisation.
Results: Our results showed that the ILF2 copy number variation (CNV) is positively correlated with ILF2 mRNA expression (r = 0.68, p < .0001). Additionally, ILF2 expression is significantly increased with melanoma progression (p < .0001), and significantly associated with poor overall survival for metastatic melanoma patients (p = .026). The overexpression of ILF2 (ILF2-OV) promotes proliferation in metastatic melanoma cells, whereas ILF2 knockdown decreases proliferation by blocking the cell cycle. Mechanistically, we demonstrated the interaction between ILF2 and the splicing factor U2AF2, whose knockdown reverses the proliferation effects mediated by ILF2-OV. Stage IIIB-C melanoma patients with high ILF2-U2AF2 expression showed significantly shorter overall survival (p = .024). Enhanced ILF2/U2AF2 expression promotes a more efficient DNA-damage repair by increasing RAD50 and ATM mRNA expression. Paradoxically, metastatic melanoma cells with ILF2-OV were more sensitive to ATM inhibitors.
Conclusion: Our study uncovered that ILF2 amplification of the 1q21.3 chromosome is associated with melanoma progression and triggers a functional downstream pathway in metastatic melanoma promoting drug resistance.
(© 2021 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.)
Databáze: MEDLINE
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