Actionable Strategies to Target Multiple Myeloma Plasma Cell Resistance/Resilience to Stress: Insights From "Omics" Research.

Omics analyses autophagy proteotoxic stress response replication stress therapeutic targets

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2020
Historique:
received: 25 02 2020
accepted: 23 04 2020
entrez: 6 6 2020
pubmed: 6 6 2020
medline: 6 6 2020
Statut: epublish

Résumé

While the modern therapeutic armamentarium to treat multiple myeloma (MM) patients allows a longer control of the disease, this second-most-frequent hematologic cancer is still uncurable in the vast majority of cases. Since MM plasma cells are subjected to various types of chronic cellular stress and the integrity of specific stress-coping pathways is essential to ensure MM cell survival, not surprisingly the most efficacious anti-MM therapy are those that make use of proteasome inhibitors and/or immunomodulatory drugs, which target the biochemical mechanisms of stress management. Based on this notion, the recently realized discoveries on MM pathobiology through high-throughput techniques (genomic, transcriptomic, and other "omics"), in order for them to be clinically useful, should be elaborated to identify novel vulnerabilities in this disease. This groundwork of information will likely allow the design of novel therapies against targetable molecules/pathways, in an unprecedented opportunity to change the management of MM according to the principle of "precision medicine." In this review, we will discuss some examples of therapeutically actionable molecules and pathways related to the regulation of cellular fitness and stress resistance in MM.

Identifiants

pubmed: 32500036
doi: 10.3389/fonc.2020.00802
pmc: PMC7243738
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

802

Informations de copyright

Copyright © 2020 Manni, Fregnani, Barilà, Zambello, Semenzato and Piazza.

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Auteurs

Sabrina Manni (S)

Department of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.

Anna Fregnani (A)

Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.
Department of Surgery, Oncology and Gastroenterology (DISCOG), University of Padova, Padova, Italy.

Gregorio Barilà (G)

Department of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.

Renato Zambello (R)

Department of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.

Gianpietro Semenzato (G)

Department of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.

Francesco Piazza (F)

Department of Medicine, Hematology and Clinical Immunology Branch, University of Padova, Padova, Italy.
Foundation for Advanced Biomedical Research - Veneto Institute of Molecular Medicine (FABR-VIMM), Padova, Italy.

Classifications MeSH