Evidence map›Paper›PMID 32825834›Full record

ArticleJournal of ovarian research2020

Neoadjuvant metformin added to conventional chemotherapy synergizes anti-proliferative effects in ovarian cancer.

Kuo-Chang Wen, Pi-Lin Sung, Alexander T H Wu, Ping-Chieh Chou, Jun-Hung Lin, Chi-Ying F Huang, Sai-Ching J Yeung, Mong-Hong Lee

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

16 citing papers in PubMed, 24 citations in OpenAlex.

  1. Trial
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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

8 authors at 6 institutions in 3 countries.

Kuo-Chang WenDepartment of Obstetrics and Gynecology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, 23561, Taiwan.ORCID http://orcid.org/0000-0001-6967-8037
Pi-Lin SungDepartment of Obstetrics and Gynecology, Shuang Ho Hospital, Taipei Medical University, New Taipei City, 23561, Taiwan.
Alexander T H WuThe Ph.D. Program for Translational Medicine, Taipei Medical University, Taipei, 11031, Taiwan.
Ping-Chieh ChouDepartment of Molecular and Cellular Oncology, Division of Basic Science Research, The University of Texas MD Anderson Cancer Center, Houston, TX, 77030, USA.
Jun-Hung LinDepartment of Obstetrics and Gynecology, Taipei Veterans General Hospital and School of Medicine, National Yang-Ming University, Taipei, 11221, Taiwan.
Chi-Ying F HuangInstitute of Biopharmaceutical Sciences, National Yang-Ming University, Taipei, 11221, Taiwan.
Sai-Ching J YeungDepartment of Emergency Medicine, Division of Internal Medicine, The University of Texas, MD Anderson Cancer Center, Houston, TX, 77030, USA. syeung@mdanderson.org.
Mong-Hong LeeGuangdong Research Institute of Gastroenterology, The Sixth Affiliated Hospital of Sun Yat-sen University, 26 Yuancun Erheng Rd, Guangzhou, 510655, P.R. China. limh33@mail.sysu.edu.cn.
National Yang Ming Chiao Tung University · TWThe University of Texas MD Anderson Cancer Center · USMin Sheng General Hospital · TWSun Yat-sen University · CNTaipei Medical University · TWTaipei Medical University-Shuang Ho Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOvarian cancer is the leading cause of cancer-related death among women. Complete cytoreductive surgery followed by platinum-taxene chemotherapy has been the gold standard for a long time. Various compounds have been assessed in an attempt to combine them with conventional chemotherapy to improve survival rates or even overcome chemoresistance. Many studies have shown that an antidiabetic drug, metformin, has cytotoxic activity in different cancer models. However, the synergism of metformin as a neoadjuvant formula plus chemotherapy in clinical trials and basic studies remains unclear for ovarian cancer.

methodsWe applied two clinical databases to survey metformin use and ovarian cancer survival rate. The Cancer Genome Atlas dataset, an L1000 microarray with Gene Set Enrichment Analysis (GSEA) analysis, Western blot analysis and an animal model were used to study the activity of the AKT/mTOR pathway in response to the synergistic effects of neoadjuvant metformin combined with chemotherapy.

resultsWe found that ovarian cancer patients treated with metformin had significantly longer overall survival than patients treated without metformin. The protein profile induced by low- concentration metformin in ovarian cancer predominantly involved the AKT/mTOR pathway. In combination with chemotherapy, the neoadjuvant metformin protocol showed beneficial synergistic effects in vitro and in vivo.

conclusionsThis study shows that neoadjuvant metformin at clinically relevant dosages is efficacious in treating ovarian cancer, and the results can be used to guide clinical trials.

Indexed as

AnimalsAntineoplastic AgentsCarboplatinDrug SynergismFemaleHumansMetforminMiceNeoadjuvant TherapyOvarian NeoplasmsProto-Oncogene Proteins c-aktSignal TransductionSurvival AnalysisTOR Serine-Threonine KinasesTreatment OutcomeXenograft Model Antitumor AssaysAntineoplastic AgentsCarboplatinMetforminMTOR protein, humanProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesAKT/mTOR pathwayClinically relevant dosageNeoadjuvant metforminOvarian cancerSynergistic effects

Identifiers

PMID32825834
PMCPMC7442990
OpenAlexW3080994564

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.