Evidence map›Paper›PMID 34873466›Full record

ArticleAmerican journal of cancer research2021

Highly potent dopamine receptor D2 antagonist ONC206 demonstrates anti-tumorigenic activity in endometrial cancer.

Allison Staley, Katherine Tucker, Yajie Yin, Xin Zhang, Yali Fan, Yingao Zhang, Ziwei Fang, Wenchuan Sun, Hongyan Suo, Xiaoling Zhao and 5 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed, 15 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

15 authors at 2 institutions in 1 country.

Allison StaleyDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Katherine TuckerDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Yajie YinDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Xin ZhangDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Yali FanDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Yingao ZhangDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Ziwei FangDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Wenchuan SunDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Hongyan SuoDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Xiaoling ZhaoDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Ziyi ZhaoDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Varun Vijay PrabhuChimerix Durham, NC 27713, USA.
Joshua E AllenChimerix Durham, NC 27713, USA.
Chunxiao ZhouDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
Victoria L Bae-JumpDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC 27599, USA.
University of North Carolina at Chapel Hill · USOncoceutics (United States) · US

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

Endometrial cancer (EC) is a highly obesity-driven cancer, with limited treatment options. ONC201 is an imipridone that selectively antagonizes the G protein-coupled receptors dopamine receptor D2 and D3 (DRD2/3) and activates human mitochondrial caseinolytic protease P (ClpP). It is a promising first-in-class small molecule that has been reported to have anti-neoplastic activity in various types of cancer through induction of the integrated stress response (ISR) as well as through stimulation of tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) and subsequent induction of apoptosis. ONC201 is being evaluated in Phase II clinical trials for solid tumors and hematological malignancies, including EC. ONC206 is an analog of ONC201 with nanomolar potency in Phase I clinical trials. This study evaluated the anti-tumor efficacy of ONC206 in EC cell lines and the

Indexed as

apoptosisdopamine receptorsendometrial cancerobesityONC206

Identifiers

PMID34873466
PMCPMC8640798
OpenAlexW4206896208

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.