Cardiovascular Complications in Patients with Prostate Cancer: Potential Molecular Connections.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
10 Apr 2023
Historique:
received: 31 01 2023
revised: 21 03 2023
accepted: 30 03 2023
medline: 1 5 2023
pubmed: 28 4 2023
entrez: 28 4 2023
Statut: epublish

Résumé

Cardiovascular diseases (CVDs) and complications are often seen in patients with prostate cancer (PCa) and affect their clinical management. Despite acceptable safety profiles and patient compliance, androgen deprivation therapy (ADT), the mainstay of PCa treatment and chemotherapy, has increased cardiovascular risks and metabolic syndromes in patients. A growing body of evidence also suggests that patients with pre-existing cardiovascular conditions show an increased incidence of PCa and present with fatal forms of the disease. Therefore, it is possible that a molecular link exists between the two diseases, which has not yet been unraveled. This article provides insight into the connection between PCa and CVDs. In this context, we present our findings linking PCa progression with patients' cardiovascular health by performing a comprehensive gene expression study, gene set enrichment (GSEA) and biological pathway analysis using publicly available data extracted from patients with advanced metastatic PCa. We also discuss the common androgen deprivation strategies and CVDs most frequently reported in PCa patients and present evidence from various clinical trials that suggest that therapy induces CVD in PCa patients.

Identifiants

pubmed: 37108147
pii: ijms24086984
doi: 10.3390/ijms24086984
pmc: PMC10138415
pii:
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Sooraj Kakkat (S)

Department of Pathology, University of South Alabama, Mobile, AL 36617, USA.
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.

Paramahansa Pramanik (P)

Department of Mathematics and Statistics, University of South Alabama, Mobile, AL 36688, USA.

Seema Singh (S)

Department of Pathology, University of South Alabama, Mobile, AL 36617, USA.
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.
Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL 36688, USA.

Ajay Pratap Singh (AP)

Department of Pathology, University of South Alabama, Mobile, AL 36617, USA.
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.
Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL 36688, USA.

Chandrani Sarkar (C)

Department of Pathology, University of South Alabama, Mobile, AL 36617, USA.
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.
Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL 36688, USA.

Debanjan Chakroborty (D)

Department of Pathology, University of South Alabama, Mobile, AL 36617, USA.
Cancer Biology Program, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA.
Department of Biochemistry and Molecular Biology, University of South Alabama, Mobile, AL 36688, USA.

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Classifications MeSH