Angiogenesis in the Normal Adrenal Fetal Cortex and Adrenocortical Tumors.

adrenal fetal cortex adrenocortical carcinoma adrenocortical tumors angiogenesis anti-angiogenic drugs

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
01 Mar 2021
Historique:
received: 31 12 2020
revised: 18 02 2021
accepted: 24 02 2021
entrez: 3 4 2021
pubmed: 4 4 2021
medline: 4 4 2021
Statut: epublish

Résumé

Angiogenesis plays an important role in several physiological and pathological processes. Pharmacological angiogenesis modulation has been robustly demonstrated to achieve clinical benefits in several cancers. Adrenocortical carcinomas (ACC) are rare tumors that often have a poor prognosis. In addition, therapeutic options for ACC are limited. Understanding the mechanisms that regulate adrenocortical angiogenesis along the embryonic development and in ACC could provide important clues on how these processes could be pharmacologically modulated for ACC treatment. In this report, we performed an integrative review on adrenal cortex angiogenesis regulation in physiological conditions and ACC. During embryonic development, adrenal angiogenesis is regulated by both VEGF and Ang-Tie signaling pathways. In ACC, early research efforts were focused on VEGF signaling and this pathway was identified as a good prognostic factor and thus a promising therapeutic target. However, every clinical trial so far conducted in ACC using VEGF pathway- targeting drugs, alone or in combination, yielded disappointing results. In contrast, although the Ang-Tie pathway has been pointed out as an important regulator of fetal adrenocortical angiogenesis, its role is yet to be explored in ACC. In the future, further research on the role and efficacy of modulating both Ang-Tie and VEGF pathways in ACC is needed.

Identifiants

pubmed: 33804534
pii: cancers13051030
doi: 10.3390/cancers13051030
pmc: PMC7957756
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : Fundação para a Ciência e a Tecnologia
ID : PTDC/MEC-ONC/31384/2017
Organisme : Fundação para a Ciência e a Tecnologia
ID : UIDB/00215/2020
Organisme : Fundação para a Ciência e a Tecnologia
ID : UIDP/00215/2020

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Auteurs

Sofia S Pereira (SS)

Department of Anatomy, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, 4050-313 Porto, Portugal.
Clinical and Experimental Endocrinology, Multidisciplinary Unit for Biomedical Research (UMIB), 4050-313 Porto, Portugal.
Instituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, 4200-135 Porto, Portugal.
Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), 4200-135 Porto, Portugal.

Sofia Oliveira (S)

Department of Anatomy, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, 4050-313 Porto, Portugal.
Faculty of Sciences, University of Porto, 4169-007 Porto, Portugal.

Mariana P Monteiro (MP)

Department of Anatomy, Instituto de Ciências Biomédicas Abel Salazar, University of Porto, 4050-313 Porto, Portugal.
Clinical and Experimental Endocrinology, Multidisciplinary Unit for Biomedical Research (UMIB), 4050-313 Porto, Portugal.

Duarte Pignatelli (D)

Instituto de Investigação e Inovação em Saúde (I3S), Universidade do Porto, 4200-135 Porto, Portugal.
Institute of Molecular Pathology and Immunology, University of Porto (IPATIMUP), 4200-135 Porto, Portugal.
Department of Endocrinology, Hospital S. João, 4200-319 Porto, Portugal.
Department of Biomedicine, Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal.

Classifications MeSH