Evidence map›Paper›PMID 24812268›Full record

ArticleCancer research2014

Say no to DMSO: dimethylsulfoxide inactivates cisplatin, carboplatin, and other platinum complexes.

Matthew D Hall, Katherine A Telma, Ki-Eun Chang, Tobie D Lee, James P Madigan, John R Lloyd, Ian S Goldlust, James D Hoeschele, Michael M Gottesman

Abstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed
16.7field-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

122 citing papers in PubMed, 368 citations in OpenAlex.

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62 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

9 authors at 5 institutions in 2 countries.

Matthew D HallAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute;
Katherine A TelmaAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute;
Ki-Eun ChangAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute;
Tobie D LeeAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute;
James P MadiganAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute;
John R LloydAdvanced Mass Spectrometry Facility, National Institute of Diabetes & Digestive & Kidney Diseases, NIH, Bethesda;
Ian S GoldlustDivision of Preclinical Innovation, National Institutes of Health Chemical Genomics Center, National Center for Advancing Translational Sciences, NIH, Rockville, Maryland; and.
James D HoescheleDepartment of Chemistry, Eastern Michigan University, Ypsilanti, Michigan.
Michael M GottesmanAuthors' Affiliations: Laboratory of Cell Biology, Center for Cancer Research, National Cancer Institute; gottesmm@mail.nih.gov.
Cancer Institute (WIA) · INCenter for Cancer Research · USEastern Michigan University · USNational Institute of Diabetes and Digestive and Kidney Diseases · USNational Institutes of Health · US

Funding

NIH Chemical Genomics CenterZIBTR000004 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI MCKEW, JOHN · 2012 to 2014
$52.3M
Mechanisms of non-classical multidrug resistance in cancerZIABC010830 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI GOTTESMAN, MICHAEL · 2009 to 2025
$19.6M
Howard Hughes Medical InstituteIntramural NIH HHS Z99 TR999999Intramural NIH HHS ZIA BC010830
6 · The paper itself

Abstract

The platinum drugs cisplatin, carboplatin, and oxaliplatin are highly utilized in the clinic and as a consequence are extensively studied in the laboratory setting. In this study, we examined the literature and found a significant number of studies (11%-34%) in prominent cancer journals utilizing cisplatin dissolved in DMSO. However, dissolving cisplatin in DMSO for laboratory-based studies results in ligand displacement and changes to the structure of the complex. We examined the effect of DMSO on platinum complexes, including cisplatin, carboplatin, and oxaliplatin, finding that DMSO reacted with the complexes, inhibited their cytotoxicity and their ability to initiate cell death. These results render a substantial portion of the literature on cisplatin uninterpretable. Raising awareness of this significant issue in the cancer biology community is critical, and we make recommendations on appropriate solvation of platinum drugs for research.

Indexed as

Antineoplastic AgentsCarboplatinCell Line, TumorCisplatinDimethyl SulfoxideHumansInhibitory Concentration 50Platinum CompoundsSolventsAntineoplastic AgentsCarboplatinCisplatinDimethyl SulfoxidePlatinum CompoundsSolvents

Identifiers

PMID24812268
PMCPMC4153432
OpenAlexW1965889589

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.