Evidence map›Paper›PMID 20541702›Full record

ArticleCancer cell2010

Enhancing tumor-specific uptake of the anticancer drug cisplatin with a copper chelator.

Seiko Ishida, Frank McCormick, Karen Smith-McCune, Douglas Hanahan

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
13.1field-weighted citation impact, top 1% 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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it, 287 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Cuproplasia and cuproptosis, two sides of the coin.Cancer communications (London, England) · 2025
    Review
  11. Article
  12. Involvement of copper in cell death and cancer.Apoptosis : an international journal on programmed cell death · 2025
    Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Article
  19. Autophagy-mediated ID1 turnover dictates chemo-resistant fate in ovarian cancer stem cells.Journal of experimental & clinical cancer research : CR · 2024
    Article
  20. Review

78 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Seiko IshidaHelen Diller Family Comprehensive Cancer Center, University of California, San Francisco, San Francisco, CA 94143, USA.
Frank McCormick
Karen Smith-McCune
Douglas Hanahan
UCSF Helen Diller Family Comprehensive Cancer Center · USUniversity of California, San Francisco · US

Funding

ROLE OF ALLELIC IMBALANCE IN OVARIAN CANCER PROGRESSIONP01CA064602 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI JAFFE, ROBERT B · 1996 to 2005
$11.3M
Stage- &cell-specific targeting of RTK in tumorigenesisR01CA099948 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BERGERS, GABRIELE, HANAHAN, DOUGLAS · 2003 to 2012
$5.1M
TARGETED ONCOGENESIS AND DIABETESR37CA045234 · NCI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI HANAHAN, DOUGLAS · 1997 to 2004
$2.2M
GENETIC CONTROL OF THE YEAST SPORULATION PROGRAMR01GM059256 · NIGMS · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI KORNBERG, THOMAS B. · 2000 to 2003
$937k
NCI NIH HHS P01 CA064602NCI NIH HHS P01CA64602NCI NIH HHS R01 CA099948NCI NIH HHS R37 CA045234NIGMS NIH HHS GM59256NIGMS NIH HHS R01 GM059256
6 · The paper itself

Abstract

Uptake of the anticancer drug cisplatin is mediated by the copper transporter CTR1 in cultured cells. Here we show in human ovarian tumors that low levels of Ctr1 mRNA are associated with poor clinical response to platinum-based therapy. Using a mouse model of human cervical cancer, we demonstrate that combined treatment with a copper chelator and cisplatin increases cisplatin-DNA adduct levels in cancerous but not in normal tissues, impairs angiogenesis, and improves therapeutic efficacy. The copper chelator also enhances the killing of cultured human cervical and ovarian cancer cells with cisplatin. Our results identify the copper transporter as a therapeutic target, which can be manipulated with copper chelating drugs to selectively enhance the benefits of platinum-containing chemotherapeutic agents.

Indexed as

Adenosine TriphosphatasesAdjuvants, PharmaceuticAdultAgedAged, 80 and overAnimalsAnimal StructuresCarboplatinCation Transport ProteinsCell Line, TumorCell ProliferationCell SurvivalChelating AgentsCisplatinCopperCopper Transporter 1Adenosine TriphosphatasesAdjuvants, PharmaceuticAtp7a protein, mouseCarboplatinCation Transport ProteinsChelating AgentsCisplatinCopperCopper Transporter 1Copper-Transporting ATPasesDNA AdductsMolybdenumSLC31A1 protein, humantetrathiomolybdate

Identifiers

PMID20541702
PMCPMC2902369
OpenAlexW2016203478

What OpenQuestion holds

Textmetadata
LicenceTDM
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.