HSP90 Molecular Chaperones, Metabolic Rewiring, and Epigenetics: Impact on Tumor Progression and Perspective for Anticancer Therapy.


Journal

Cells
ISSN: 2073-4409
Titre abrégé: Cells
Pays: Switzerland
ID NLM: 101600052

Informations de publication

Date de publication:
03 06 2019
Historique:
received: 22 03 2019
revised: 30 05 2019
accepted: 31 05 2019
entrez: 6 6 2019
pubmed: 6 6 2019
medline: 6 6 2019
Statut: epublish

Résumé

Heat shock protein 90 (HSP90) molecular chaperones are a family of ubiquitous proteins participating in several cellular functions through the regulation of folding and/or assembly of large multiprotein complexes and client proteins. Thus, HSP90s chaperones are, directly or indirectly, master regulators of a variety of cellular processes, such as adaptation to stress, cell proliferation, motility, angiogenesis, and signal transduction. In recent years, it has been proposed that HSP90s play a crucial role in carcinogenesis as regulators of genotype-to-phenotype interplay. Indeed, HSP90 chaperones control metabolic rewiring, a hallmark of cancer cells, and influence the transcription of several of the key-genes responsible for tumorigenesis and cancer progression, through either direct binding to chromatin or through the quality control of transcription factors and epigenetic effectors. In this review, we will revise evidence suggesting how this interplay between epigenetics and metabolism may affect oncogenesis. We will examine the effect of metabolic rewiring on the accumulation of specific metabolites, and the changes in the availability of epigenetic co-factors and how this process can be controlled by HSP90 molecular chaperones. Understanding deeply the relationship between epigenetic and metabolism could disclose novel therapeutic scenarios that may lead to improvements in cancer treatment.

Identifiants

pubmed: 31163702
pii: cells8060532
doi: 10.3390/cells8060532
pmc: PMC6627532
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
HSP90 Heat-Shock Proteins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

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Auteurs

Valentina Condelli (V)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. valentina.condelli@crob.it.

Fabiana Crispo (F)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. fabiana.crispo@crob.it.

Michele Pietrafesa (M)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. michele.pietrafesa@crob.it.

Giacomo Lettini (G)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. giacomo.lettini@crob.it.

Danilo Swann Matassa (DS)

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy. daniloswann.matassa@unina.it.

Franca Esposito (F)

Department of Molecular Medicine and Medical Biotechnology, University of Naples Federico II, 80131 Naples, Italy. franca.esposito@unina.it.

Matteo Landriscina (M)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. matteo.landriscina@unifg.it.
Medical Oncology Unit, Department of Medical and Surgical Sciences, University of Foggia, 71100 Foggia, Italy. matteo.landriscina@unifg.it.

Francesca Maddalena (F)

Laboratory of Pre-Clinical and Translational Research, IRCCS, Referral Cancer Center of Basilicata, 85028 Rionero in Vulture, PZ, Italy. francesca.maddalena@crob.it.

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