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Isoform-Directed Control of c-Myc Functions: Understanding the Balance from Proliferation to Growth Arrest

A. Kubickova, JB. De Sanctis, M. Hajduch

. 2023 ; 24 (24) : . [pub] 20231215

Language English Country Switzerland

Document type Journal Article, Review

Grant support
LM2018133 Ministry of Youth, School, Education and Sport of the Czech Republic
LX22NPO5102 Ministry of Youth, School, Education and Sport of the Czech Republic

The transcription factor c-Myc, a key regulator of cellular processes, has long been associated with roles in cell proliferation and apoptosis. This review analyses the multiple functions of c-Myc by examining the different c-Myc isoforms in detail. The impact of different c-Myc isoforms, in particular p64 and p67, on fundamental biological processes remains controversial. It is necessary to investigate the different isoforms in the context of proto-oncogenesis. The current knowledge base suggests that neoplastic lesions may possess the means for self-destruction via increased c-Myc activity. This review presents the most relevant information on the c-Myc locus and focuses on a number of isoforms, including p64 and p67. This compilation provides a basis for the development of therapeutic approaches that target the potent growth arresting and pro-apoptotic functions of c-Myc. This information can then be used to develop targeted interventions against specific isoforms with the aim of shifting the oncogenic effects of c-Myc from pro-proliferative to pro-apoptotic. The research summarised in this review can deepen our understanding of how c-Myc activity contributes to different cellular responses, which will be crucial in developing effective therapeutic strategies; for example, isoform-specific approaches may allow for precise modulation of c-Myc function.

References provided by Crossref.org

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