Apoptosis Inhibitor 5: A Multifaceted Regulator of Cell Fate

Author:

Abbas Hafsia1,Derkaoui Dalia Kheira1,Jeammet Louise2,Adicéam Emilie2,Tiollier Jérôme2,Sicard Hélène2,Braun Thorsten345,Poyet Jean-Luc67ORCID

Affiliation:

1. Université Oran 1, Ahmed Ben Bella, Oran 31000, Algeria

2. Jalon Therapeutics, 75010 Paris, France

3. Laboratoire de Transfert des Leucémies, EA3518, Institut de Recherche Saint Louis, Hôpital Saint Louis, Université de Paris, 75010 Paris, France

4. AP-HP, Service d’Hématologie Clinique, Hôpital Avicenne, Université Paris XIII, 93000 Bobigny, France

5. OPALE Carnot Institute, The Organization for Partnerships in Leukemia, Hôpital Saint-Louis, 75010 Paris, France

6. INSERM UMRS976, Institut de Recherche Saint Louis, Hôpital Saint Louis, 75010 Paris, France

7. Université Paris Cité, 75015 Paris, France

Abstract

Apoptosis, or programmed cell death, is a fundamental process that maintains tissue homeostasis, eliminates damaged or infected cells, and plays a crucial role in various biological phenomena. The deregulation of apoptosis is involved in many human diseases, including cancer. One of the emerging players in the intricate regulatory network of apoptosis is apoptosis inhibitor 5 (API5), also called AAC-11 (anti-apoptosis clone 11) or FIF (fibroblast growth factor-2 interacting factor). While it may not have yet the same level of notoriety as some other cancer-associated proteins, API5 has garnered increasing attention in the cancer field in recent years, as elevated API5 levels are often associated with aggressive tumor behavior, resistance to therapy, and poor patient prognosis. This review aims to shed light on the multifaceted functions and regulatory mechanisms of API5 in cell fate decisions as well as its interest as therapeutic target in cancer.

Funder

Inserm

Publisher

MDPI AG

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