Evidence map›Paper›PMID 24419103›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2014

Targeting estrogen-related receptor alpha inhibits epithelial-to-mesenchymal transition and stem cell properties of ovarian cancer cells.

Sophia Sn Lam, Abby Sc Mak, Judy Wp Yam, Annie Ny Cheung, Hextan Ys Ngan, Alice St Wong

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 64 citations in OpenAlex.

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  11. Expression of estrogen-related receptors in ovarian cancer and impact on survival.Journal of cancer research and clinical oncology · 2021
    Article
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  16. Presence and role of stem cells in ovarian cancer.World journal of stem cells · 2019
    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 1 institution in 1 country.

Sophia Sn LamSchool of Biological Sciences, University of Hong Kong, Pokfulam Road, Pokfulam, Hong Kong.
Abby Sc MakSchool of Biological Sciences, University of Hong Kong, Pokfulam Road, Pokfulam, Hong Kong.
Judy Wp YamDepartment of Pathology, University of Hong Kong, Sassoon Road, Pokfulam, Hong Kong.
Annie Ny CheungDepartment of Pathology, University of Hong Kong, Sassoon Road, Pokfulam, Hong Kong.
Hextan Ys NganDepartment of Obstetrics and Gynecology, University of Hong Kong, Sassoon Road, Pokfulam, Hong Kong.
Alice St WongSchool of Biological Sciences, University of Hong Kong, Pokfulam Road, Pokfulam, Hong Kong.
University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial-mesenchymal transition represents a key event in cancer progression and has emerged as a promising anticancer target. Estrogen-related receptor alpha (ERRα) is frequently elevated in advanced-stage ovarian cancer, but its potential role in tumor progression is not known. Here we show that ERRα functions in epithelial-mesenchymal transition and in subsequent stem cell traits responsible for the acquisition of high degree of aggressiveness and potential for metastasis that are characteristic of ovarian cancer. Importantly, targeted inhibition of ERRα also inhibited the expression of Snail, a repressor of E-cadherin and an inducer of epithelial-mesenchymal transition. Interestingly, induction of Snail resulted from not only changes in mRNA transcription rate but also mRNA stability. We thus identified the miR-200 family as a new player in the ERRα-mediated posttranscriptional regulation of Snail, and antagonism of miR-200a/b could revert the decreased expression of Snail and reversal of epithelial-mesenchymal transition and stem cell characteristics due to ERRα depletion. Finally, we showed that RNA interference-mediated inhibition of ERRα significantly reduced tumor burden, ascites formation, and metastatic peritoneal nodules in vivo in an orthotopic model of ovarian cancer. These results suggest ERRα activation as a mechanism of tumor aggressiveness and imply that targeting ERRα may be a promising approach in ovarian cancer treatment.

Indexed as

Genetic TherapyAnimalsCell Line, TumorEpithelial-Mesenchymal TransitionERRalpha Estrogen-Related ReceptorFemaleHumansMolecular Targeted TherapyNeoplastic Stem CellsOvarian NeoplasmsReceptors, EstrogenSnailsTranscription, GeneticERRalpha Estrogen-Related ReceptorReceptors, Estrogen

Identifiers

PMID24419103
PMCPMC3982489
OpenAlexW2023243872

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.