Evidence map›Paper›PMID 26433846›Full record

ReviewDermatologic clinics2015

Methotrexate and Pralatrexate.

Gary S Wood, Jianqiang Wu

Open access · hybridAbstract readReview
In one paragraph

Review in Dermatologic clinics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 59 citations in OpenAlex.

  1. Trial
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  10. How to Sequence Therapies in Mycosis Fungoides.Current treatment options in oncology · 2021
    Review
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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

2 authors at 1 institution in 1 country.

Gary S WoodDepartment of Dermatology, University of Wisconsin and VA Medical Center, 7th Floor, One South Park, Madison, WI 53715, USA. Electronic address: gwood@dermatology.wisc.edu.
Jianqiang WuDepartment of Dermatology, University of Wisconsin and VA Medical Center, 7th Floor, One South Park, Madison, WI 53715, USA.
University of Wisconsin–Madison · US

Funding

FAS Pathway Abnormalities in MF and SSI01BX002204 · VA · WM S. MIDDLETON MEMORIAL VETERANS HOSP · PI WOOD, GARY S · 2015 to 2018
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BLRD VA I01 BX002204
6 · The paper itself

Abstract

This article reviews methotrexate and the more potent, related compound, pralatrexate, for the treatment of cutaneous T-cell lymphomas, including mycosis fungoides, Sézary syndrome, and CD30+ lymphoproliferative disorders. Although these folate antagonists are traditionally viewed as antiproliferative cell cycle inhibitors, it is recognized that they inhibit DNA methylation, providing a rationale for their use as epigenetic regulators and cell proliferation inhibitors. The underlying mechanisms are outlined, key supporting data presented, followed by brief mention of recent mathematical modeling supporting the general superiority of combination therapy. Several novel examples involving folate antagonists are proposed.

Indexed as

AminopterinAntimetabolites, AntineoplasticApoptosisDNA MethylationEpigenesis, GeneticFolic Acid AntagonistsHumansLymphoma, T-Cell, CutaneousMethotrexateSkin NeoplasmsS Phase10-propargyl-10-deazaaminopterinAminopterinAntimetabolites, AntineoplasticFolic Acid AntagonistsMethotrexateApoptosisDihydrofolate reductaseFolateFolic acidMethotrexatePralatrexatePurine synthesisS phase

Identifiers

PMID26433846
PMCPMC5549926
OpenAlexW2105529781

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.