Evidence map›Paper›PMID 30538112›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2019

Identification and Characterization of Synthetic Viability with ERCC1 Deficiency in Response to Interstrand Crosslinks in Lung Cancer.

Joshua R Heyza, Wen Lei, Donovan Watza, Hao Zhang, Wei Chen, Jessica B Back, Ann G Schwartz, Gerold Bepler, Steve M Patrick

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Multi-Scale Imaging of the Dynamic Organization of Chromatin.International journal of molecular sciences · 2023
    Review
  5. Progress and Perspective of CRISPR-Cas9 Technology in Translational Medicine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2023
    Review
  6. Article
  7. Applications and advancements of CRISPR-Cas in the treatment of lung cancer.Frontiers in cell and developmental biology · 2023
    Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Joshua R HeyzaDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Wen LeiDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Donovan WatzaDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Hao ZhangDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Wei ChenDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Jessica B BackDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.
Ann G SchwartzDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan.ORCID https://orcid.org/0000-0002-9525-1157
Gerold BeplerDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan. patricks@karmanos.org beplerg@karmanos.org.
Steve M PatrickDepartment of Oncology, Karmanos Cancer Institute and Wayne State University, Detroit, Michigan. patricks@karmanos.org beplerg@karmanos.org.
The Barbara Ann Karmanos Cancer Institute · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Inflammation Pathways and COPD in the Development of Lung CancerR01CA141769 · NCI · WAYNE STATE UNIVERSITY · PI SCHWARTZ, ANN G. · 2011 to 2016
$8.7M
TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA141769NCI NIH HHS T32 CA009531
6 · The paper itself

Abstract

purposeERCC1/XPF is a DNA endonuclease with variable expression in primary tumor specimens, and has been investigated as a predictive biomarker for efficacy of platinum-based chemotherapy. The failure of clinical trials utilizing ERCC1 expression to predict response to platinum-based chemotherapy suggests additional mechanisms underlying the basic biology of ERCC1 in the response to interstrand crosslinks (ICLs) remain unknown. We aimed to characterize a panel of ERCC1 knockout (Δ) cell lines, where we identified a synthetic viable phenotype in response to ICLs with ERCC1 deficiency. EXPERIMENTAL

designWe utilized the CRISPR-Cas9 system to create a panel of ERCC1Δ lung cancer cell lines which we characterized.

resultsWe observe that loss of ERCC1 hypersensitizes cells to cisplatin when wild-type (WT) p53 is retained, whereas there is only modest sensitivity in cell lines that are p53

conclusionsOur findings implicate p53 as a potential confounding variable in clinical assessments of ERCC1 as a platinum biomarker via promoting an environment in which error-prone mechanisms of ICL-R may be able to partially compensate for loss of ERCC1.

Indexed as

Lung NeoplasmsCisplatinDNA-Binding ProteinsDNA RepairEndonucleasesHumansCisplatinDNA-Binding ProteinsEndonucleasesERCC1 protein, human

Identifiers

PMID30538112
PMCPMC6467763
OpenAlexW2905124326

What OpenQuestion holds

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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.