Evidence map›Paper›PMID 31815044›Full record

ArticleAmerican journal of cancer research2019

BRCA1 identified as a modulator of temozolomide resistance in P53 wild-type GBM using a high-throughput shRNA-based synthetic lethality screening.

Jie Ding, Shaofang Wu, Chen Zhang, Arnav Garyali, Emmanuel Martinez-Ledesma, Feng Gao, Adarsha Pokkulandra, Xiaolong Li, Christopher Bristow, Alessandro Carugo and 2 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Role of BRCA1 in glioblastoma etiology.Cellular oncology (Dordrecht, Netherlands) · 2024
    Review
  3. Article
  4. Article
  5. Article
  6. 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

12 authors at 1 institution in 2 countries.

Jie DingDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Shaofang WuDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Chen ZhangDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Arnav GaryaliDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Emmanuel Martinez-LedesmaDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Feng GaoDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Adarsha PokkulandraDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Xiaolong LiDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Christopher BristowDepartment of Applied Cancer Science, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Alessandro CarugoDepartment of Applied Cancer Science, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Dimpy KoulDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
Wk Alfred YungDepartment of Neuro-Oncology, Brain Tumor Center, The University of Texas MD Anderson Cancer Center Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
Tropism Enhanced Oncolytic Adenovirus for the Treatment of Brain TumorsP50CA127001 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Juan Fueyo · 2008 to 2026
$41.2M
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA127001
6 · The paper itself

Abstract

Glioblastoma multiforme (GBM), the most common type of primary brain tumor, is universally fatal, with a median survival duration ranging from 12-15 months despite maximum treatment efforts. Temozolomide (TMZ) is the current standard of care for GBM patients; however patients usually develop resistance to TMZ and limits its benefit. The identification of novel synergistic targets in GBM will lead to the development of new targeted drugs, which could be combined with broad-spectrum cytotoxic agents. In this study, we used a high-throughput synthetic lethality screen with a pooled short hairpin DNA repair library, in combination with TMZ, to identify targets that will enhance TMZ-induced antitumor effects. Using an unbiased bioinformatical analysis, we identified BRCA1 as a potential promising candidate gene that induced synthetic lethality with TMZ in glioma sphere-forming cells (GSCs). BRCA1 knockdown resulted in antitumor activity with TMZ in P53 wild-type GSCs but not in P53 mutant GSCs. TMZ treatment induced a DNA damage repair response; the activation of BRCA1 DNA repair pathway targets and knockdown of BRCA1, together with TMZ, led to increased DNA damage and cell death in P53 wild-type GSCs. Our study identified BRCA1 as a potential target that sensitizes TMZ-induced cell death in P53 wild-type GBM, suggesting that the combined inhibition of BRCA1 and TMZ treatment will be a successful targeted therapy for GBM patients.

Indexed as

apoptosisBRCA1Synthetic lethalityTMZ

Identifiers

PMID31815044
PMCPMC6895442
OpenAlexW2998633657

What OpenQuestion holds

Textmetadata
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.