Evidence map›Paper›PMID 30400270›Full record

ArticleNutrients2018

Targeting the DNA Repair Endonuclease ERCC1-XPF with Green Tea Polyphenol Epigallocatechin-3-Gallate (EGCG) and Its Prodrug to Enhance Cisplatin Efficacy in Human Cancer Cells.

Joshua R Heyza, Sanjeevani Arora, Hao Zhang, Kayla L Conner, Wen Lei, Ashley M Floyd, Rahul R Deshmukh, Jeffrey Sarver, Christopher J Trabbic, Paul Erhardt and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Xeroderma pigmentosum with multiple skin carcinoma and a homogenousThe Journal of international medical research · 2026
    Review
  7. Review
  8. Review
  9. Review
  10. mAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Anticarcinogenic potentials of tea catechins.Frontiers in nutrition · 2022
    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

13 authors at 3 institutions in 3 countries.

Joshua R HeyzaDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. jrheyza@med.wayne.edu.
Sanjeevani AroraDepartment of Cancer Biology, University of Toledo Health Science Campus, Toledo, OH 43614, USA. sanjeevani.arora@fccc.edu.
Hao ZhangDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. hzhang1@hfhs.org.
Kayla L ConnerDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. connerk@karmanos.org.
Wen LeiDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. leiwen314@gmail.com.
Ashley M FloydDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. floyda@karmanos.org.
Rahul R DeshmukhDepartment of Pathology, Wayne State University School of Medicine, Detroit, MI 48201, USA. rdeshmukh@lecom.edu.
Jeffrey SarverDepartment of Pharmacology and Experimental Therapeutics, University of Toledo College of Pharmacy and Pharmaceutical Sciences, Toledo, OH 43614, USA. jeffrey.sarver@utoledo.edu.
Christopher J TrabbicCenter for Drug Design and Development, Department of Medicinal and Biological Chemistry, University of Toledo College of Pharmacy and Pharmaceutical Sciences, Toledo, OH 43614, USA. christrabbic51@gmail.com.
Paul ErhardtCenter for Drug Design and Development, Department of Medicinal and Biological Chemistry, University of Toledo College of Pharmacy and Pharmaceutical Sciences, Toledo, OH 43614, USA. paul.erhardt@utoledo.edu.
Tak-Hang ChanState Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hong Kong, China. tak-hang.chan@mcgill.ca.ORCID 0000-0002-8702-4499
Q Ping DouDepartments of Oncology, Pharmacology, and Pathology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. doup@karmanos.org.
Steve M PatrickDepartment of Oncology, Karmanos Cancer Institute, Wayne State University, Detroit, MI 48201, USA. patricks@karmanos.org.
Wayne State University · USUniversity of Toledo · USHong Kong Polytechnic University · HK

Funding

TRAINING PROGRAM IN THE BIOLOGY OF CANCERT32CA009531 · NCI · WAYNE STATE UNIVERSITY · PI Larry H Matherly · 1985 to 2026
$5.3M
Novel Role of Base Excision Repair and Mismatch Repair in Cisplatin SensitivityR01GM088249 · NIGMS · WAYNE STATE UNIVERSITY · PI PATRICK, STEVE M · 2010 to 2014
$1.4M
American Cancer Society RSG-06-163-01Natural Sciences and Engineering Research Council of Canada awarded to Tak-Hang ChanNCI NIH HHS CA009035NCI NIH HHS T32CA009531NIGMS NIH HHS R01 GM088249NIH HHS 1R01CA120009NIH HHS 1R01GM088249NIH HHS 5R03CA112625U.S. Department of Defense CA171000
6 · The paper itself

Abstract

The 5'-3' structure-specific endonuclease ERCC1/XPF (Excision Repair Cross-Complementation Group 1/Xeroderma Pigmentosum group F) plays critical roles in the repair of cisplatin-induced DNA damage. As such, it has been identified as a potential pharmacological target for enhancing clinical response to platinum-based chemotherapy. The goal of this study was to follow up on our previous identification of the compound NSC143099 as a potent inhibitor of ERCC1/XPF activity by performing an in silico screen to identify structural analogues that could inhibit ERCC1/XPF activity in vitro and in vivo. Using a fluorescence-based DNA-endonuclease incision assay, we identified the green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG) as a potent inhibitor of ERCC1/XPF activity with an IC

Indexed as

AnimalsApoptosisCatechinCell Line, TumorCell ProliferationCisplatinComet AssayDNA-Binding ProteinsDNA RepairDrug Resistance, NeoplasmEndonucleasesFemaleHumansMiceMice, NudePlatinumCatechinCisplatinDNA-Binding ProteinsEndonucleasesepigallocatechin gallateERCC1 protein, humanPlatinumPolyphenolsProdrugsTeaxeroderma pigmentosum group F proteinchemoresistancecisplatinDNA repairERCC1/XPFgreen tea polyphenols

Identifiers

PMID30400270
PMCPMC6267282
OpenAlexW2898632463

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.