Dynamics of ARF regulation that control senescence and cancer

Aram Ko, Su Yeon Han, Jaewhan Song

Research output: Contribution to journalReview articlepeer-review

14 Citations (Scopus)

Abstract

ARF is an alternative reading frame product of the INK4a/ARF locus, inactivated in numerous human cancers. ARF is a key regulator of cellular senescence, an irreversible cell growth arrest that suppresses tumor cell growth. It functions by sequestering MDM2 (a p53 E3 ligase) in the nucleolus, thus activating p53. Besides MDM2, ARF has numerous other interacting partners that induce either cellular senescence or apoptosis in a p53-independent manner. This further complicates the dynamics of the ARF network. Expression of ARF is frequently disrupted in human cancers, mainly due to epigenetic and transcriptional regulation. Vigorous studies on various transcription factors that either positively or negatively regulate ARF transcription have been carried out. However, recent focus on posttranslational modifications, particularly ubiquitination, indicates wider dynamic controls of ARF than previously known. In this review, we discuss the role and dynamic regulation of ARF in senescence and cancer.

Original languageEnglish
Pages (from-to)598-606
Number of pages9
JournalBMB reports
Volume49
Issue number11
DOIs
Publication statusPublished - 2016

Bibliographical note

Funding Information:
This work is supported by the Basic Science Research Program of the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (2014R1A1A1002589) and the Korea Healthcare Technology R&D Project, Ministry for Health & Welfare Affairs, Republic of Korea (A121387).

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology

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