Evidence map›Paper›PMID 35582008›Full record

ReviewCancer drug resistance (Alhambra, Calif.)2021

The role of extracellular vesicles in acquisition of resistance to therapy in glioblastomas.

Anudeep Yekula, Abigail Taylor, Alexandra Beecroft, Keiko M Kang, Julia L Small, Koushik Muralidharan, Zachary Rosh, Bob S Carter, Leonora Balaj

Open access · diamondAbstract readReview
In one paragraph

Review in Cancer drug resistance (Alhambra, Calif.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  5. Article
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  9. Computational Mutagenesis and Inhibition ofBioMed research international · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Overcoming drug resistance in glioblastoma: new options in sight?Cancer drug resistance (Alhambra, Calif.) · 2021
    Article
  17. Review
  18. 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

9 authors at 2 institutions in 1 country.

Anudeep YekulaDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Abigail TaylorBrigham Young University, Provo, UT 84602, USA.
Alexandra BeecroftBrigham Young University, Provo, UT 84602, USA.
Keiko M KangDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Julia L SmallDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Koushik MuralidharanDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Zachary RoshDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Bob S CarterDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Leonora BalajDepartment of Neurosurgery, Massachusetts General Hospital, Boston, MA 02114, USA.
Massachusetts General Hospital · USBrigham Young University · US

Funding

Imaging and Liquid Biopsy for Glioma Diagnosis and Treatment MonitoringR01CA239078 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI BALAJ, LEONORA, LEE, HAKHO · 2020 to 2024
$3.1M
Standardized Molecular Analyses of Glioma EVsR01CA237500 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI CARTER, BOB S, LEE, HAKHO · 2020 to 2024
$3.0M
NCI NIH HHS R01 CA237500NCI NIH HHS R01 CA239078
6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive primary brain tumor with a median survival of 15 months despite standard care therapy consisting of maximal surgical debulking, followed by radiation therapy with concurrent and adjuvant temozolomide treatment. The natural history of GBM is characterized by inevitable recurrence with patients dying from increasingly resistant tumor regrowth after therapy. Several mechanisms including inter- and intratumoral heterogeneity, the evolution of therapy-resistant clonal subpopulations, reacquisition of stemness in glioblastoma stem cells, multiple drug efflux mechanisms, the tumor-promoting microenvironment, metabolic adaptations, and enhanced repair of drug-induced DNA damage have been implicated in therapy failure. Extracellular vesicles (EVs) have emerged as crucial mediators in the maintenance and establishment of GBM. Multiple seminal studies have uncovered the multi-dynamic role of EVs in the acquisition of drug resistance. Mechanisms include EV-mediated cargo transfer and EVs functioning as drug efflux channels and decoys for antibody-based therapies. In this review, we discuss the various mechanisms of therapy resistance in GBM, highlighting the emerging role of EV-orchestrated drug resistance. Understanding the landscape of GBM resistance is critical in devising novel therapeutic approaches to fight this deadly disease.

Indexed as

extracellular vesiclesGlioblastomaradiationresistancetemozolomide

Identifiers

PMID35582008
PMCPMC9019190
OpenAlexW3099403605

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.