Evidence map›Paper›PMID 30210923›Full record

ArticleAmerican journal of cancer research2018

ONC201 demonstrates anti-tumorigenic and anti-metastatic activity in uterine serous carcinoma in vitro.

Ziwei Fang, Jiandong Wang, Leslie H Clark, Wenchuan Sun, Yajie Yin, Weimin Kong, Stuart R Pierce, Lindsay West, Stephanie A Sullivan, Arthur-Quan Tran and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  11. Article
  12. Raw Lacquer Extract from Toxicodendron vernicifluum in Combination with ONC201 Enhances the Inhibitory Effects on Colorectal Cancer Cell Activity.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2023
    Article
  13. Therapeutic targeting of TRAIL death receptors.Biochemical Society transactions · 2023
    Review
  14. Article
  15. Article
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  18. Article
  19. Targeting dopamine receptor D2 as a novel therapeutic strategy in endometrial cancer.Journal of experimental & clinical cancer research : CR · 2021
    Article
  20. Article
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.

Ziwei FangDepartment of Obstetrics, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, P. R. China.
Jiandong WangDepartment of Gynecologic Oncology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, P. R. China.
Leslie H ClarkDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Wenchuan SunDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Yajie YinDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Weimin KongDepartment of Gynecologic Oncology, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing, P. R. China.
Stuart R PierceDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Lindsay WestDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Stephanie A SullivanDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Arthur-Quan TranDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Varun V PrabhuOncoceutics Philadelphia, PA, USA.
Chunxiao ZhouDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
Victoria Bae-JumpDivision of Gynecologic Oncology, University of North Carolina at Chapel Hill Chapel Hill, NC, USA.
University of North Carolina at Chapel Hill · USBeijing Obstetrics and Gynecology Hospital · 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

Uterine serous carcinoma (USC) represents an aggressive histologic subtype of endometrial cancer. It is associated with a poor prognosis, and improved therapies for women battling USCs are greatly needed. ONC201 is an orally bioavailable, first-in-class small molecule that induces tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) independent of p53. ONC201 has demonstrated anti-tumorigenic activity in pre-clinical models of solid tumors through induction of apoptosis and inactivation of the AKT/MAPK pathways. Recent phase I and II clinical trials have shown that ONC201 is well tolerated and may have single agent activity in high grade glioma patients among others. We sought to determine the effects of ONC201 on cell proliferation in USC and identify the mechanisms by which ONC201 inhibits cell growth in this disease. ONC201 inhibited cell proliferation in a dose-dependent manner in ARK1, ARK2 and SPEC-2 cell lines. The anti-proliferative activity of ONC201 in ARK1 and SPEC-2 cells was associated with induction apoptosis independent of p53 via both a TRAIL mediated apoptotic pathway and a mitochondrial apoptosis pathway. Treatment with ONC201 resulted in significant reduction in adhesion and invasion as well as inhibition of the AKT and MAPK pathways. In addition, ONC201 markedly potentiated the anti-tumorigenic effects of paclitaxel in USC cells. Our results suggest that ONC201 has significant anti-proliferative and anti-metastatic effects in USC cells through both induction of apoptosis and inhibition of the AKT and MAPK pathways. ONC201 and paclitaxel are a promising therapeutic combination in USC cells. Thus, ONC201 should be evaluated as a single agent and as a therapeutic partner with paclitaxel in future clinical trials of USC.

Indexed as

apoptosiscell proliferationinvasionONC201uterine serous carcinoma

Identifiers

PMID30210923
PMCPMC6129479
OpenAlexW2981427587

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.