Effect of MYC and PARP Inhibitors in Ovarian Cancer Using an


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
May 2024
Historique:
received: 23 01 2024
revised: 06 03 2024
accepted: 08 03 2024
medline: 28 4 2024
pubmed: 28 4 2024
entrez: 27 4 2024
Statut: ppublish

Résumé

The 8q24 chromosomal region, which contains the MYC and PVT1 candidate oncogenes, is amplified in carcinomas. Both genes have been involved in the etiopathogenesis of ovarian cancer (OC). In this study, we used an in vitro OC model with a known 8q24 copy number increase and in silico tools to investigate the expression of MYC/PVT1 loci and copy number variation in OC. We also assessed the effects of rucaparib (a PARP inhibitor) in the presence or absence of 10058F4 (a MYC inhibitor) on the expression of MYC/linear PVT1/circular PVT1. Tissue culture, chromosome preparation, RNA extraction, RT-qPCR, FISH, and wound healing assays were employed. OncoDB, cBioportal, UALKAN, and ROC Plotter in silico tools were also utilized. Although PVT1 and MYC expression levels remained unaltered in OC, putative copy number alterations across all cancers showed a marked difference between the two genes, particularly in gain and amplification for MYC. PVT1 expression demonstrated prognostic value for the treatment of patients with serous and endometrioid OC. Both genes correlated with PARP10, FAM83H, and DEPTOR. The use of rucaparib in the presence or absence of the MYC inhibitor (10058F4) in vitro, led to a significant down-regulation in the expression of MYC, linear, and circular PVT1. Our data provide a novel insight into the potential interactions of MYC and PVT1 with other genes. Moreover, we identified a new PARP inhibition mechanism down-regulating MYC, as well as the linear and circular PVT1 transcripts. Future work should expand on clinical studies to better understand the prognostic role of PVT1 in OC.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
The 8q24 chromosomal region, which contains the MYC and PVT1 candidate oncogenes, is amplified in carcinomas. Both genes have been involved in the etiopathogenesis of ovarian cancer (OC). In this study, we used an in vitro OC model with a known 8q24 copy number increase and in silico tools to investigate the expression of MYC/PVT1 loci and copy number variation in OC. We also assessed the effects of rucaparib (a PARP inhibitor) in the presence or absence of 10058F4 (a MYC inhibitor) on the expression of MYC/linear PVT1/circular PVT1.
MATERIALS AND METHODS METHODS
Tissue culture, chromosome preparation, RNA extraction, RT-qPCR, FISH, and wound healing assays were employed. OncoDB, cBioportal, UALKAN, and ROC Plotter in silico tools were also utilized.
RESULTS RESULTS
Although PVT1 and MYC expression levels remained unaltered in OC, putative copy number alterations across all cancers showed a marked difference between the two genes, particularly in gain and amplification for MYC. PVT1 expression demonstrated prognostic value for the treatment of patients with serous and endometrioid OC. Both genes correlated with PARP10, FAM83H, and DEPTOR. The use of rucaparib in the presence or absence of the MYC inhibitor (10058F4) in vitro, led to a significant down-regulation in the expression of MYC, linear, and circular PVT1.
CONCLUSION CONCLUSIONS
Our data provide a novel insight into the potential interactions of MYC and PVT1 with other genes. Moreover, we identified a new PARP inhibition mechanism down-regulating MYC, as well as the linear and circular PVT1 transcripts. Future work should expand on clinical studies to better understand the prognostic role of PVT1 in OC.

Identifiants

pubmed: 38677725
pii: 44/5/1817
doi: 10.21873/anticanres.16983
doi:

Substances chimiques

Poly(ADP-ribose) Polymerase Inhibitors 0
Proto-Oncogene Proteins c-myc 0
rucaparib 8237F3U7EH
Indoles 0
MYC protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1817-1827

Informations de copyright

Copyright © 2024 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Alessandro Morea (A)

IFOM ETS - The AIRC Institute of Molecular Oncology, Milan, Italy.

Sayeh Saravi (S)

Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, U.K.

Cristina Sisu (C)

Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, U.K.

Marcia Hall (M)

Mount Vernon Cancer Centre, Northwood, U.K.

Sabrina Tosi (S)

Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, U.K.

Emmanouil Karteris (E)

Department of Life Sciences, College of Health, Medicine and Life Sciences, Brunel University London, Uxbridge, U.K.; Emmanouil.Karteris@brunel.ac.uk.

Clelia Tiziana Storlazzi (CT)

Department of Biosciences, Biotechnology and Environment, University of Bari Aldo Moro, Bari, Italy cleliatiziana.storlazzi@uniba.it.

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Classifications MeSH