Evidence map›Paper›PMID 33194693›Full record

ArticleFrontiers in oncology2020

ONC206, an Imipridone Derivative, Induces Cell Death Through Activation of the Integrated Stress Response in Serous Endometrial Cancer

Yingao Zhang, Yu Huang, Yajie Yin, Yali Fan, Wenchuan Sun, Xiaoling Zhao, Katherine Tucker, Allison Staley, Sarah Paraghamian, Gabrielle Hawkins and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 25 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

14 authors at 3 institutions in 2 countries.

Yingao ZhangDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Yu HuangDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Yajie YinDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Yali FanDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Wenchuan SunDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Xiaoling ZhaoDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Katherine TuckerDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Allison StaleyDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Sarah ParaghamianDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Gabrielle HawkinsDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Varun PrabhuOncoceutics, Philadelphia, PA, United States.
Joshua E AllenOncoceutics, Philadelphia, PA, United States.
Chunxiao ZhouDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
Victoria Bae-JumpDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.
University of North Carolina at Chapel Hill · USOncoceutics (United States) · USCapital Medical University · CN

Funding

Obesity-driven Metabolic and Molecular Biomarkers of Metformin Response in Endometrial CancerR37CA226969 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAE-JUMP, VICTORIA LIN · 2018 to 2024
$2.5M
NCI NIH HHS R37 CA226969
6 · The paper itself

Abstract

ONC206 (Oncoceutics) is an imipiridone with nanomolar potency and analogue of ONC201, a selective dopamine receptor D2 (DRD2) antagonist currently being investigated in phase II clinical trials for serous endometrial cancer (SEC). This study investigated the anti-proliferative efficacy of ONC206 in SEC cell lines as well as its impact on cellular stress and adhesion/invasion. ONC206 inhibited cellular proliferation in a dose-dependent manner and was more potent than ONC201 in the ARK1 (IC

Indexed as

cellular stressinvasionONC206proliferationserous endometrial cancer

Identifiers

PMID33194693
PMCPMC7641618
OpenAlexW3094049949

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.