Fatty acid synthase as a potential new therapeutic target for cervical cancer.


Journal

Anais da Academia Brasileira de Ciencias
ISSN: 1678-2690
Titre abrégé: An Acad Bras Cienc
Pays: Brazil
ID NLM: 7503280

Informations de publication

Date de publication:
2022
Historique:
received: 28 04 2021
accepted: 24 06 2021
entrez: 4 5 2022
pubmed: 5 5 2022
medline: 7 5 2022
Statut: epublish

Résumé

Fatty acid synthase (FASN) is the rate-limiting enzyme for the de novo synthesis of fatty acids in the cytoplasm of tumour cells. Many tumour cells express high levels of FASN, and its expression is associated with a poorer prognosis. Cervical cancer is a major public health problem, representing the fourth most common cancer affecting women worldwide. To date, only a few in silico studies have correlated FASN expression with cervical cancer. This study aimed to investigate in vitro FASN expression in premalignant lesions and cervical cancer samples and the effects of a FASN inhibitor on cervical cancer cells. FASN expression was observed in all cervical cancer samples with increased expression at more advanced cervical cancer stages. The FASN inhibitor (orlistat) reduced the in vitro cell viability of cervical cancer cells (C-33A, ME-180, HeLa and SiHa) in a time-dependent manner and triggered apoptosis. FASN inhibitor also led to cell cycle arrest and autophagy. FASN may be a potential therapeutic target for cervical cancer, and medicinal chemists, pharmaceutical researchers and formulators should consider this finding in the development of new treatment approaches for this cancer type.

Identifiants

pubmed: 35507982
pii: S0001-37652022000300705
doi: 10.1590/0001-3765202220210670
pii:
doi:

Substances chimiques

Orlistat 95M8R751W8
Fatty Acid Synthases EC 2.3.1.85

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e20210670

Auteurs

Jéssica Nascimento (J)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Camila Mariot (C)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Débora R B Vianna (DRB)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Lúcia M Kliemann (LM)

Universidade Federal do Rio Grande do Sul, Hospital de Clínicas de Porto Alegre e Faculdade de Medicina, Departamento de Patologia, Rua Ramiro Barcelos, 2400, 90035-002 Porto Alegre, RS, Brazil.

Paula S Chaves (PS)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Massimo Loda (M)

Weil Cornell Medicine, Department of Pathology and Laboratory Medicine, 1300 York Avenue, New York Presbyterian-Weill Cornell Campus, New York, NY, 10065, USA.
New York Genome Center Affiliate Member, 101 Avenue of the Americas, New York, NY, 10013, USA.
Broad Institute of MIT and Harvard University, 415 Main Street, Cambridge, MA, 2142, USA.

Andréia Buffon (A)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Ruy C R Beck (RCR)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

Diogo A Pilger (DA)

Universidade Federal do Rio Grande do Sul, Faculdade de Farmácia, Av. Ipiranga, 2752, 90610-000 Porto Alegre, RS, Brazil.

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Classifications MeSH