» Articles » PMID: 32842503

Angiogenesis Inhibition in Prostate Cancer: An Update

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2020 Aug 27
PMID 32842503
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Prostate cancer (PCa), like all other solid tumors, relies on angiogenesis for growth, progression, and the dissemination of tumor cells to other parts of the body. Despite data from in vitro and in vivo preclinical studies, as well as human specimen studies indicating the crucial role played by angiogenesis in PCa, angiogenesis inhibition in clinical settings has not shown significant benefits to patients, thus challenging the inclusion and usefulness of antiangiogenic agents for the treatment of PCa. However, one of the apparent reasons why these antiangiogenic agents failed to meet expectations in PCa can be due to the choice of the antiangiogenic agents, because the majority of these drugs target vascular endothelial growth factor-A (VEGFA) and its receptors. The other relevant causes might be inappropriate drug combinations, the duration of treatment, and the method of endpoint determination. In this review, we will first discuss the role of angiogenesis in PCa growth and progression. We will then summarize the different angiogenic growth factors that influence PCa growth dynamics and review the outcomes of clinical trials conducted with antiangiogenic agents in PCa patients and, finally, critically assess the current status and fate of antiangiogenic therapy in this disease.

Citing Articles

Prostate cancer microenvironment: multidimensional regulation of immune cells, vascular system, stromal cells, and microbiota.

Chen L, Xu Y, Wang Y, Ren Y, Dong X, Wu P Mol Cancer. 2024; 23(1):229.

PMID: 39395984 PMC: 11470719. DOI: 10.1186/s12943-024-02137-1.


Growth Factors and Their Application in the Therapy of Hereditary Neurodegenerative Diseases.

Issa S, Fayoud H, Shaimardanova A, Sufianov A, Sufianova G, Solovyeva V Biomedicines. 2024; 12(8).

PMID: 39200370 PMC: 11351319. DOI: 10.3390/biomedicines12081906.


MYC and p53 alterations cooperate through VEGF signaling to repress cytotoxic T cell and immunotherapy responses in prostate cancer.

Murphy K, DeMarco K, Zhou L, Lopez-Diaz Y, Ho Y, Li J bioRxiv. 2024; .

PMID: 39091883 PMC: 11291169. DOI: 10.1101/2024.07.24.604943.


Analysis of the Gene Networks and Pathways Correlated with Tissue Differentiation in Prostate Cancer.

Filippi A, Aurelian J, Mocanu M Int J Mol Sci. 2024; 25(7).

PMID: 38612439 PMC: 11011430. DOI: 10.3390/ijms25073626.


Prostate Cancer Microvascular Routes: Exploration and Measurement Strategies.

Grizzi F, Hegazi M, Zanoni M, Vota P, Toia G, Clementi M Life (Basel). 2023; 13(10).

PMID: 37895416 PMC: 10608780. DOI: 10.3390/life13102034.


References
1.
Salameh A, Lee A, Cardo-Vila M, Nunes D, Efstathiou E, Staquicini F . PRUNE2 is a human prostate cancer suppressor regulated by the intronic long noncoding RNA PCA3. Proc Natl Acad Sci U S A. 2015; 112(27):8403-8. PMC: 4500257. DOI: 10.1073/pnas.1507882112. View

2.
Picus J, Halabi S, Kelly W, Vogelzang N, Whang Y, Kaplan E . A phase 2 study of estramustine, docetaxel, and bevacizumab in men with castrate-resistant prostate cancer: results from Cancer and Leukemia Group B Study 90006. Cancer. 2010; 117(3):526-33. PMC: 3010428. DOI: 10.1002/cncr.25421. View

3.
Dandekar D, Lokeshwar B . Inhibition of cyclooxygenase (COX)-2 expression by Tet-inducible COX-2 antisense cDNA in hormone-refractory prostate cancer significantly slows tumor growth and improves efficacy of chemotherapeutic drugs. Clin Cancer Res. 2004; 10(23):8037-47. DOI: 10.1158/1078-0432.CCR-04-1208. View

4.
Thomson A . Role of androgens and fibroblast growth factors in prostatic development. Reproduction. 2001; 121(2):187-95. DOI: 10.1530/rep.0.1210187. View

5.
de Bono J, Scher H, Montgomery R, Parker C, Miller M, Tissing H . Circulating tumor cells predict survival benefit from treatment in metastatic castration-resistant prostate cancer. Clin Cancer Res. 2008; 14(19):6302-9. DOI: 10.1158/1078-0432.CCR-08-0872. View