Therapeutic Application of Brain-Specific Angiogenesis Inhibitor 1 for Cancer Therapy.

Vasculostatin (Vstat120) brain-specific angiogenesis inhibitor 1 (BAI1) glioblastoma (GBM) oncolytic herpes simplex virus-1 (oHSV)

Journal

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

Informations de publication

Date de publication:
16 Jul 2021
Historique:
received: 29 05 2021
revised: 07 07 2021
accepted: 13 07 2021
entrez: 24 7 2021
pubmed: 25 7 2021
medline: 25 7 2021
Statut: epublish

Résumé

Brain-specific angiogenesis inhibitor 1 (BAI1/ADGRB1) is an adhesion G protein-coupled receptor that has been found to play key roles in phagocytosis, inflammation, synaptogenesis, the inhibition of angiogenesis, and myoblast fusion. As the name suggests, it is primarily expressed in the brain, with a high expression in the normal adult and developing brain. Additionally, its expression is reduced in brain cancers, such as glioblastoma (GBM) and peripheral cancers, suggesting that BAI1 is a tumor suppressor gene. Several investigators have demonstrated that the restoration of BAI1 expression in cancer cells results in reduced tumor growth and angiogenesis. Its expression has also been shown to be inversely correlated with tumor progression, neovascularization, and peri-tumoral brain edema. One method of restoring BAI1 expression is by using oncolytic virus (OV) therapy, a strategy which has been tested in various tumor models. Oncolytic herpes simplex viruses engineered to express the secreted fragment of BAI1, called Vasculostatin (Vstat120), have shown potent anti-tumor and anti-angiogenic effects in multiple tumor models. Combining Vstat120-expressing oHSVs with other chemotherapeutic agents has also shown to increase the overall anti-tumor efficacy in both in vitro and in vivo models. In the current review, we describe the structure and function of BAI1 and summarize its application in the context of cancer treatment.

Identifiants

pubmed: 34298774
pii: cancers13143562
doi: 10.3390/cancers13143562
pmc: PMC8303278
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Subventions

Organisme : American Cancer Society
ID : RSG-19-185-01-MPC
Organisme : NIH HHS
ID : R01 CA150153
Pays : United States
Organisme : NIH HHS
ID : R61NS112410
Pays : United States
Organisme : NIH HHS
ID : R03 CA252770
Pays : United States
Organisme : Cancer Prevention and Research Institute of Texas
ID : High Impact/High Risk grant (RP200615)

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Auteurs

Mitra Nair (M)

Department of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Department of Pediatric Surgery-Regenerative Medicine, McGovern Medical School, The University of Texas Health Science, Houston, TX 77030, USA.

Chelsea Bolyard (C)

The Pelotonia Institute for Immuno-Oncology, The Ohio State University Comprehensive Cancer Center, The Ohio State University Wexner Medical Center, Columbus, OH 43210, USA.

Tae Jin Lee (TJ)

Department of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Balveen Kaur (B)

Department of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Ji Young Yoo (JY)

Department of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.

Classifications MeSH