Evidence map›Paper›PMID 26942921›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2016

Valproic acid inhibits the angiogenic potential of cervical cancer cells via HIF-1α/VEGF signals.

Y Zhao, W You, J Zheng, Y Chi, W Tang, R Du

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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2016. 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
1.2field-weighted citation impact, top 20% 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, 30 citations in OpenAlex.

  1. Review
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  4. Short-chain fatty acids in cancer pathogenesis.Cancer metastasis reviews · 2023
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  9. [MiR-600 suppresses HeLa cell proliferation by inhibiting hypoxia-inducible factor-1Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2021
    Article
  10. International journal of molecular sciences · 2020
    Article
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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 1 institution in 1 country.

Y ZhaoDepartment of Obstetrics and Gynecology, Liaocheng Second People's Hospital, Liaocheng, 252600, China.
W YouDepartment of Obstetrics and Gynecology, Liaocheng People's Hospital, No. 45, Huashan Road, Development Area, Liaocheng, Shandong, 252000, China. youweizhilc@126.com.
J ZhengDepartment of Obstetrics and Gynecology, Liaocheng Third People's Hospital, Liaocheng, 252000, China.
Y ChiDepartment of Obstetrics and Gynecology, Liaocheng Second People's Hospital, Liaocheng, 252600, China.
W TangCentral Laboratory, Liaocheng People's Hospital, Liaocheng, 252000, China.
R DuCentral Laboratory, Liaocheng People's Hospital, Liaocheng, 252000, China.
Liaocheng People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCervical cancer is one of the most prevalent malignancies in women worldwide. Therefore, the investigation about the molecular pathogenesis and related therapy targets of cervical cancer is an emergency. The objective of the present study is to investigate the effects of valproic acid (VPA), a histone deacetylase inhibitor, on the angiogenesis of cervical cancer.

methodsThe effects and mechanisms of VPA on in vitro angiogenesis and vascular endothelial growth factor (VEGF) expression of human cervical cancer HeLa and SiHa cells were investigated.

resultsOur present study reveals that 1 mM VPA can significantly inhibit the in vitro angiogenic potential and VEGF expression of human cervical cancer HeLa and SiHa cells. Further, the transcription and protein levels of hypoxia inducible factor-1α (HIF-1α), and not HIF-1β, are significantly inhibited in VPA-treated cervical cancer cells. Over expression of HIF-1α can obviously reverse VPA-induced VEGF down regulation. VPA-treatment decreases the activation of Akt and ERK1/2 in both HeLa and SiHa cells in a time-dependent manner. The inhibitor of Akt (LY 294002) or ERK1/2 (PD98059) can inhibit VEGF alone and cooperatively reinforce the suppression effects of VPA on HIF-1α and VEGF expression.

conclusionCollectively, our data reveal that the inhibition of PI3K/Akt and ERK1/2 signals are involved in VPA-induced HIF-1α and VEGF suppression of cervical cancer cells.

Indexed as

Angiogenesis InhibitorsBlotting, WesternCell Line, TumorCell ProliferationEnzyme-Linked Immunosorbent AssayFemaleHumansHypoxia-Inducible Factor 1, alpha SubunitNeovascularization, PathologicReal-Time Polymerase Chain ReactionSignal TransductionUterine Cervical NeoplasmsValproic AcidVascular Endothelial Growth Factor AAngiogenesis InhibitorsHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitValproic AcidVascular Endothelial Growth Factor AVEGFA protein, humanAngiogenesisCervical cancerHIF-1αValproic acidVEGF

Identifiers

PMID26942921
OpenAlexW2302716119

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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.