Literature DB >> 34310025

Understanding MCL1: from cellular function and regulation to pharmacological inhibition.

Mónica Sancho1, Diego Leiva1, Estefanía Lucendo1, Mar Orzáez1.   

Abstract

Myeloid cell leukemia-1 (MCL1), an antiapoptotic member of the BCL2 family characterized by a short half-life, functions as a rapid sensor that regulates cell death and other relevant processes that include cell cycle progression and mitochondrial homeostasis. In cancer, MCL1 overexpression contributes to cell survival and resistance to diverse chemotherapeutic agents; for this reason, several MCL1 inhibitors are currently under preclinical and clinical development for cancer treatment. However, the nonapoptotic functions of MCL1 may influence their therapeutic potential. Overall, the complexity of MCL1 regulation and function represent challenges to the clinical application of MCL1 inhibitors. We now summarize the current knowledge regarding MCL1 structure, regulation, and function that could impact the clinical success of MCL1 inhibitors.
© 2021 The Authors. The FEBS Journal published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies.

Entities:  

Keywords:  BCL2 family; MCL1; MCL1 inhibitor; apoptosis; cell cycle

Mesh:

Substances:

Year:  2021        PMID: 34310025     DOI: 10.1111/febs.16136

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.622


  2 in total

1.  Scaffold hopping from indoles to indazoles yields dual MCL-1/BCL-2 inhibitors from MCL-1 selective leads.

Authors:  Brandon Drennen; Christopher C Goodis; Nathan Bowen; Wenbo Yu; Gregory Vickers; Paul T Wilder; Alexander D MacKerell; Steven Fletcher
Journal:  RSC Med Chem       Date:  2022-06-03

2.  Identification and Validation of an Apoptosis-Related Gene Prognostic Signature for Oral Squamous Cell Carcinoma.

Authors:  Shuqin Wang; Sien Zhang; Zhi Lin; Jingxin Ma; Lijun Zhu; Guiqing Liao
Journal:  Front Oncol       Date:  2022-06-13       Impact factor: 5.738

  2 in total

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