Evidence map›Paper›PMID 34948433›Full record

ReviewInternational journal of molecular sciences2021

Targeting AVIL, a New Cytoskeleton Regulator in Glioblastoma.

Robert Cornelison, Laine Marrah, Drew Horter, Sarah Lynch, Hui Li

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Rhabdomyosarcomas are oncogene addicted to the activation of AVIL.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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 1 institution in 1 country.

Robert CornelisonDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-9775-6677
Laine MarrahDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0003-1745-8539
Drew HorterDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Sarah LynchDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Hui LiDepartment of Pathology, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.ORCID 0000-0002-7879-1792
University of Virginia · US

Funding

Women's Oncology Program - WONP30CA044579 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Dina Gould Halme · 1987 to 2026
$72.1M
Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
Targeting AVIL in GlioblastomaR01CA240601 · NCI · UNIVERSITY OF VIRGINIA · PI LI, HUI · 2020 to 2024
$2.4M
NCI NIH HHS 5R01CA240601NCI NIH HHS P30 CA044579NCI NIH HHS R01 CA240601NCI NIH HHS T32 CA009109
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common adult neural malignancy and the deadliest. The standard of care is optimal, safe, cytoreductive surgery followed by combined radiation therapy and alkylating chemotherapy with temozolomide. Recurrence is common and therapeutic options in the recurrent setting are limited. The dismal prognosis of GBM has led to novel treatments being a serious roadblock in the field, with most new treatments failing to show efficacy. Targeted therapies have shown some success in many cancers, but GBM remains one of the most difficult to treat, especially in recurrence. New chemotherapeutic directions need to be explored, possibly expanding the targeted chemotherapy spectrum in previously unforeseen ways. In this perspective paper, we will explain why AVIL, an actin-binding protein recently found to be overexpressed in GBM and a driving force for GBM, could prove versatile in the fight against cancer. By looking at AVIL and its potential to regulate FOXM1 and LIN28B, we will be able to highlight a way to improve outcomes for GBM patients who normally have very little hope.

Indexed as

CytoskeletonForkhead Box Protein M1GlioblastomaHumansMicrofilament ProteinsRNA-Binding ProteinsAVIL protein, humanForkhead Box Protein M1FOXM1 protein, humanLIN28B protein, humanMicrofilament ProteinsRNA-Binding ProteinsactinAVILFOXM1gelsolinglioblastomaLIN28B

Identifiers

PMID34948433
PMCPMC8706274
OpenAlexW4200169603

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.