Evidence map›Paper›PMID 24721622›Full record

ArticleJournal of ovarian research2014

Epidermal growth factor induces platelet-activating factor production through receptors transactivation and cytosolic phospholipase A2 in ovarian cancer cells.

Yi Yu, Xiaoyan Zhang, Shanshan Hong, Mingxing Zhang, Qingqing Cai, Wei Jiang, Congjian Xu

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

14 citing papers in PubMed, 23 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

7 authors at 2 institutions in 1 country.

Yi YuObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Xiaoyan ZhangObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Shanshan HongObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Mingxing ZhangObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Qingqing CaiObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Wei JiangObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China.
Congjian XuObstetrics and Gynecology Hospital, Fudan University, No.419 Fang-Xie Road, Shanghai 200011, People's Republic of China ; Department of Obstetrics and Gynecology of Shanghai Medical School, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China ; Shanghai Key Laboratory of Female Reproductive Endocrine Related Diseases, No. 413 Zhao-Jiabang Road, Shanghai 200011, People's Republic of China ; Institute of Biomedical Sciences, Fudan University, No.138 Yi-Xueyuan Road, Shanghai 200032, People's Republic of China.
Obstetrics and Gynecology Hospital of Fudan University · CNShanghai Medical College of Fudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAmong the pro-inflammatory lipid mediators, platelet-activating factor (PAF) is a major primary and secondary messenger that binds to the PAF-receptor (PAFR). Epidermal growth factor (EGF) is a polypeptide growth factor that binds to the EGF-receptor (EGFR). Evidence suggests that both PAF and EGF play a significant role in oncogenic transformation, tumor growth, neoangiogenesis and metastasis, including ovarian cancer. PAF has the potential to transactivate EGFR in ovarian cancer cells. This study explores the mechanisms involved in EGF-induced PAF production.

methodsThe effect of EGF on PAF production in ovarian cancer cells was observed using enzyme-linked immunosorbent assay. The receptors transactivation and the role of cytosolic phospholipase A2 (cPLA2) in modulating PAF production induced by EGF was assessed using pharmacological inhibitors, si-RNA knockdown, targeted gene overexpression and immunocytochemistry. The signaling pathways invovled in PAF production induced by EGF in ovarian cancer cells were assessed.

resultsWe demonstrate that EGF increases the production of PAF in CAOV3 and SKOV3 ovarian cancer cell lines. EGF induces the transactivation of PAFR, which can be blocked by an EGFR inhibitor. Inhibition of EGFR and/or PAFR blocks PAF production in response to EGF. EGF-induced PAF production involves the phosphorylation of extracellular-regulated protein kinase (ERK) and cytosolic phospholipase A2 (cPLA2). A cPLA2 inhibitor blocks EGF-induced PAF production as well as si-cPLA2, while overexpression of cPLA2 increases PAF production.

conclusionsThese results indicate that EGF stimulates PAF production in ovarian cancer cells in a manner that requires cPLA2. We have also determined that crosstalk can occur bidirectionally between EGFR and PAFR, suggesting that EGF-induced PAF production could result in positive feedback that acts on the PAF-receptor to promote ovarian cancer progression.

Indexed as

Cell Line, TumorEpidermal Growth FactorErbB ReceptorsHumansPhospholipases A2, CytosolicPhosphorylationPlatelet Activating FactorPlatelet Membrane GlycoproteinsProtein Processing, Post-TranslationalReceptors, G-Protein-CoupledSignal TransductionTranscriptional ActivationEGFR protein, humanEpidermal Growth FactorErbB ReceptorsPhospholipases A2, CytosolicPlatelet Activating Factorplatelet activating factor receptorPlatelet Membrane GlycoproteinsReceptors, G-Protein-CoupledcPLA2EGFEGF-receptorERKOvarian cancerPAF-receptor

Identifiers

PMID24721622
PMCPMC4005630
OpenAlexW2164895930

What OpenQuestion holds

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LicenceCC BY
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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.