Evidence map›Paper›PMID 25666060›Full record

ReviewPhilosophical transactions. Series A, Mathematical, physical, and engineering sciences2015

Third row transition metals for the treatment of cancer.

Timothy C Johnstone, Kogularamanan Suntharalingam, Stephen J Lippard

Open access · bronzeAbstract readReview
In one paragraph

Review in Philosophical transactions. Series A, Mathematical, physical, and engineering sciences, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
4.7field-weighted citation impact, top 3% 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

37 citing papers in PubMed, 128 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Science advances · 2025
    Article
  6. Recent Advances in Anticancer Research of Osmium and Rhodium Complexes.Medicinal chemistry (Shariqah (United Arab Emirates)) · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Review
  16. NMR studies of group 8 metallodrugs:Dalton transactions (Cambridge, England : 2003) · 2021
    Article
  17. Article
  18. Article
  19. Arene Ruthenium(II) Complexes Bearing the κ-Molecules (Basel, Switzerland) · 2021
    Article
  20. 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

3 authors at 1 institution in 1 country.

Timothy C JohnstoneDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Kogularamanan SuntharalingamDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Stephen J LippardDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA lippard@mit.edu.
Massachusetts Institute of Technology · US

Funding

Understanding and Improving Platinum Anticancer DrugsR01CA034992 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI YILMAZ, OMER · 1985 to 2018
$6.8M
CHEMISTRY AND BIOLOGY OF PLATINUM ANTICANCER DRUGSR37CA034992 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI LIPPARD, STEPHEN J. · 1990 to 2008
$5.7M
NCI NIH HHS CA034992NCI NIH HHS R01 CA034992
6 · The paper itself

Abstract

Platinum compounds are a mainstay of cancer chemotherapy, with over 50% of patients receiving platinum. But there is a great need for improvement. Major features of the cisplatin mechanism of action involve cancer cell entry, formation mainly of intrastrand cross-links that bend and unwind nuclear DNA, transcription inhibition and induction of cell-death programmes while evading repair. Recently, we discovered that platinum cross-link formation is not essential for activity. Monofunctional Pt compounds such as phenanthriplatin, which make only a single bond to DNA nucleobases, can be far more active and effective against a range of tumour types. Without a cross-link-induced bend, monofunctional complexes can be accommodated in the major groove of DNA. Their biological mechanism of action is similar to that of cisplatin. These discoveries opened the door to a large family of heavy metal-based drug candidates, including those of Os and Re, as will be described.

Indexed as

Antineoplastic AgentsCross-Linking ReagentsDNADNA RepairDrug DesignHumansModels, ChemicalNeoplasmsPlatinumTransition ElementsAntineoplastic AgentsCross-Linking ReagentsDNAPlatinumTransition Elementsanti-cancermonofunctionalosmiumplatinumtransition metal

Identifiers

PMID25666060
PMCPMC4342973
OpenAlexW2119024264

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.