Evidence map›Paper›PMID 32382996›Full record

ArticleCellular oncology (Dordrecht, Netherlands)2020

The PI3K/mTOR dual inhibitor GSK458 potently impedes ovarian cancer tumorigenesis and metastasis.

Yangjiong Xiao, Yang Yu, Pengcheng Jiang, Yuhong Li, Chao Wang, Rong Zhang

Abstract read
In one paragraph

Article in Cellular oncology (Dordrecht, Netherlands), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
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

20 citing papers in PubMed, 36 citations in OpenAlex.

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  8. An immortalized adipose-derived stem cells line from theBiochemistry and biophysics reports · 2024
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  13. The senescence-associated secretory phenotype in ovarian cancer dissemination.American journal of physiology. Cell physiology · 2022
    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

6 authors at 4 institutions in 2 countries.

Yangjiong XiaoDepartment of Obstetrics and Gynecology, Shanghai Fengxian District Central Hospital, Southern Medical University, 201499, Shanghai, China. xiaoyangjiong@alumni.sjtu.edu.cn.ORCID http://orcid.org/0000-0002-4532-1671
Yang YuShanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences, School of Life Sciences, East China Normal University, Shanghai, 200241, China.
Pengcheng JiangDepartment of Gynecology, Changzhou Second People's Hospital Affiliated to Nanjing Medical University, Changzhou, 213004, China.
Yuhong LiDepartment of Gynecology, The International Peace Maternity & Child Health Hospital, The China Welfare Institute, Shanghai Jiaotong University, Shanghai, 200030, China.
Chao WangDepartment of Gynecology, The International Peace Maternity & Child Health Hospital, The China Welfare Institute, Shanghai Jiaotong University, Shanghai, 200030, China.
Rong ZhangDepartment of Obstetrics and Gynecology, Shanghai Fengxian District Central Hospital, Southern Medical University, 201499, Shanghai, China. rongzhang@163.com.
International Peace Maternity & Child Health Hospital · CNXian Central Hospital · CNChangzhou No.2 People's Hospital · CNEast China Normal University · CN

Funding

Major Research Plan 81472445Major Research Plan 81672587Postdoctoral Research Foundation of China 2019M652850Scientific and Innovative Action Plan of Shanghai 4411973100Young Scientists Fund 81702563
6 · The paper itself

Abstract

purposeThe PI3K/AKT/mTOR pathway is one of the most highly activated cellular signaling pathways in advanced ovarian cancer. Although several PI3K/AKT/mTOR inhibitors have been developed to treat various types of cancer, the antitumor efficacy of many of these compounds against ovarian cancer has remained unclear.

methodsHere, we tested and compared a panel of 16 PI3K/AKT/mTOR inhibitors (XL765, Miltefosine, Rapamycin, CCI-779, RAD001, FK506, XL147, GSK2110183, IPI-145, GSK2141795, BYL719, GSK458, CAL-101, XL765 analogue SAR245409, Triciribine, and GDC0941) that have entered clinical trials for antitumor activity against ovarian cancer, as well as the front line drug, paclitaxel. Antitumor efficacy was measured in both ovarian cancer cell lines and patient-derived ovarian primary tumor cell lines in vitro and in vivo.

resultsWe identified the PI3K/mTOR dual inhibitor GSK458 as a potent inhibitor of proliferation in all cell lines tested at half maximal inhibitory concentrations (IC

conclusionsBased on our results, we conclude that GSK458 may serve as an attractive candidate to treat ovarian cancer.

Indexed as

AnimalsBenzenesulfonamidesCarcinogenesisCarcinoma, Ovarian EpithelialCell Line, TumorCell ProliferationCells, CulturedFemaleHumansMiceMice, NudeOvarian NeoplasmsPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProtein Kinase InhibitorsPyridazinesBenzenesulfonamidesMTOR protein, humanomipalisibPhosphatidylinositol 3-KinasesPhosphoinositide-3 Kinase InhibitorsProtein Kinase InhibitorsPyridazinesQuinolinesSulfonamidesTOR Serine-Threonine KinasesGSK458Ovarian cancerPI3K/AKT/mTOR inhibitorPrimary cell linesTarget therapyXenograft

Identifiers

PMID32382996
PMCPMC12990695
OpenAlexW3021280920

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.