Evidence map›Paper›PMID 35261784›Full record

ArticleAmerican journal of cancer research2022

ONC206 has anti-tumorigenic effects in human ovarian cancer cells and in a transgenic mouse model of high-grade serous ovarian cancer.

Katherine Tucker, Yajie Yin, Stuart-Allison Staley, Ziyi Zhao, Ziwei Fang, Yali Fan, Xin Zhang, Hongyan Suo, Wenchuan Sun, Varun Vijay Prabhu and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

15 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  6. Review
  7. Mitochondrial Protease ClpP: Cancer Marker and Drug Target.Pharmaceuticals (Basel, Switzerland) · 2025
    Review
  8. 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

13 authors at 2 institutions in 2 countries.

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.
Stuart-Allison StaleyDivision 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.
Ziwei FangDivision 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.
Xin ZhangDivision 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.
Wenchuan SunDivision 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 · USChimerix (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

ONC206, a dopamine receptor D2 (DRD2) antagonist and imipridone, is a chemically modified derivative of ONC201. Recently, ONC206 and other imipridones were identified as activators of the mitochondrial protease ClpP, inducing downstream pathways that allow them to selectively target cancer cells. Clinical trials showed that ONC201, the first in class imipridone, was well tolerated and exhibited tumor regression in some solid tumors. Our goal was to evaluate the effect of ONC206 on cell proliferation and tumor growth in ovarian cancer cell lines and in a transgenic mouse model of high grade serous ovarian cancer (KpB model). ONC206 was more potent than ONC201 in inhibiting cell proliferation, as evidenced by a 10-fold decrease in IC50 for the SKOV3 and OVCAR5 cell lines. This was accompanied by the results that ONC206 significantly inhibited cellular proliferation, induced cell cycle G1 arrest and apoptosis, caused cellular stress, and inhibited adhesion and invasion

Indexed as

adhesion/invasionapoptosiscell proliferationONC206ovarian cancer

Identifiers

PMID35261784
PMCPMC8900003
OpenAlexW4226317856

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.