Evidence map›Paper›PMID 30836001›Full record

ArticleJournal of medicinal chemistry2019

Potent and Highly Selective Aldo-Keto Reductase 1C3 (AKR1C3) Inhibitors Act as Chemotherapeutic Potentiators in Acute Myeloid Leukemia and T-Cell Acute Lymphoblastic Leukemia.

Kshitij Verma, Tianzhu Zang, Trevor M Penning, Paul C Trippier

Open access · greenAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  4. Bioactivity profiling ofJournal of enzyme inhibition and medicinal chemistry · 2025
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  5. The structural basis of aldo-keto reductase 1C3 inhibition by 17α-picolyl and 17(Journal of enzyme inhibition and medicinal chemistry · 2025
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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

4 authors at 2 institutions in 1 country.

Kshitij VermaDepartment of Pharmaceutical Sciences , Texas Tech University Health Sciences Center, School of Pharmacy , Amarillo , Texas 79106 , United States.
Tianzhu ZangCenter of Excellence in Environmental Toxicology, Department of Systems Pharmacology & Translational Therapeutics, Perelman School of Medicine , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.
Trevor M PenningCenter of Excellence in Environmental Toxicology, Department of Systems Pharmacology & Translational Therapeutics, Perelman School of Medicine , University of Pennsylvania , Philadelphia , Pennsylvania 19104 , United States.ORCID 0000-0002-3937-1066
Paul C TrippierDepartment of Pharmaceutical Sciences , Texas Tech University Health Sciences Center, School of Pharmacy , Amarillo , Texas 79106 , United States.ORCID 0000-0002-4947-5782
Texas Tech University · USTranslational Therapeutics (United States) · US

Funding

Translational Research Support CoreP30ES013508 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI Rebecca A Simmons · 2006 to 2026
$35.3M
AKR1C Inhibitors as Chemotherapeutic PotentiatorsR01CA226436 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI TRIPPIER, PAUL · 2019 to 2023
$2.0M
NCI NIH HHS R01 CA226436NIEHS NIH HHS P30 ES013508
6 · The paper itself

Abstract

Aldo-keto reductase 1C3 (AKR1C3) catalyzes the synthesis of 9α,11β-prostaglandin (PG) F

Indexed as

Aldo-Keto Reductase Family 1 Member C3Antineoplastic AgentsCell Line, TumorCytarabineDaunorubicinDrug SynergismEnzyme InhibitorsHumansLeukemia, Myeloid, AcutePrecursor T-Cell Lymphoblastic Leukemia-LymphomaStructure-Activity RelationshipAKR1C3 protein, humanAldo-Keto Reductase Family 1 Member C3Antineoplastic AgentsCytarabineDaunorubicinEnzyme Inhibitors

Identifiers

PMID30836001
PMCPMC6528660
OpenAlexW2921102985

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.