Evidence map›Paper›PMID 29626126›Full record

ArticleMolecular cancer therapeutics2018

APTO-253 Is a New Addition to the Repertoire of Drugs that Can Exploit DNA BRCA1/2 Deficiency.

Cheng-Yu Tsai, Si Sun, Hongying Zhang, Andrea Local, Yongxuan Su, Larry A Gross, William G Rice, Stephen B Howell

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Cheng-Yu TsaiMoores Cancer Center, San Diego, California.
Si SunMoores Cancer Center, San Diego, California.
Hongying ZhangAptose Biosciences, Inc, San Diego, California.
Andrea LocalAptose Biosciences, Inc, San Diego, California.
Yongxuan SuDepartment of Chemistry and Biochemistry, University of California, San Diego, California.
Larry A GrossDepartment of Chemistry and Biochemistry, University of California, San Diego, California.
William G RiceAptose Biosciences, Inc, San Diego, California.
Stephen B HowellMoores Cancer Center, San Diego, California. showell@ucsd.edu.
Aptose Biosciences (United States) · USFleet Science Center · USUniversity of San Diego · US

Funding

VIRAL MALIGNANCYP30CA023100 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DIANE M SIMEONE · 1985 to 2026
$124.9M
NCI NIH HHS P30 CA023100
6 · The paper itself

Abstract

APTO-253 is a small molecule with antiproliferative activity against cell lines derived from a wide range of human malignancies. We sought to determine the mechanisms of action and basis for resistance to APTO-253 so as to identify synthetic lethal interactions that can guide combination studies. The cellular pharmacology of APTO-253 was analyzed in Raji lymphoma cells and a subline selected for resistance (Raji/253R). Using LC/MS/ESI analysis, APTO-253 was found to convert intracellularly to a complex containing one molecule of iron and three molecules of APTO-253 [Fe(253)

Indexed as

AnimalsAntineoplastic AgentsBRCA1 ProteinBRCA2 ProteinBreast NeoplasmsCell Line, TumorDisease Models, AnimalDNA DamageDose-Response Relationship, DrugDrug Resistance, NeoplasmFemaleHumansImidazolesPhenanthrolinesXenograft Model Antitumor AssaysAntineoplastic AgentsAPTO-253BRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanImidazolesPhenanthrolines

Identifiers

PMID29626126
PMCPMC7087411
OpenAlexW2795855802

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.