Evidence map›Paper›PMID 34298774›Full record

ReviewCancers2021

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

Mitra Nair, Chelsea Bolyard, Tae Jin Lee, Balveen Kaur, Ji Young Yoo

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.4field-weighted citation impact, top 43% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Adhesion G protein-coupled receptors.Pharmacological reviews · 2026
    Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Oncolytic Viruses: Immunotherapy Drugs for Gastrointestinal Malignant Tumors.Frontiers in cellular and infection microbiology · 2022
    Review
  11. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Mitra NairDepartment of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Chelsea BolyardThe 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 LeeDepartment of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Balveen KaurDepartment of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Ji Young YooDepartment of Neurosurgery, Mc Govern Medical School, The University of Texas Health Science Center at Houston, Houston, TX 77030, USA.ORCID 0000-0002-6767-1111
The University of Texas Health Science Center at Houston · USThe Ohio State University Wexner Medical Center · US

Funding

Enhancing Viral Oncolysis with Vasculostatin Gene DeliveryR01CA150153 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2011 to 2020
$4.0M
Optimizing oncolytic virus therapy for glioblastomaR61NS112410 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2019 to 2020
$775k
Simultaneous targeting of tumor cells and tumor associated macrophages by RNA nanovectorR03CA252770 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LEE, TAE JIN · 2021 to 2021
$156k
American Cancer Society RSG-19-185-01-MPCCancer Prevention and Research Institute of Texas High Impact/High Risk grant (RP200615)NCI NIH HHS R03 CA252770NIH HHS R01 CA150153NIH HHS R03 CA252770NIH HHS R61NS112410
6 · The paper itself

Abstract

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.

Indexed as

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

Identifiers

PMID34298774
PMCPMC8303278
OpenAlexW3185040099

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.