Evidence map›Paper›PMID 24877083›Full record

ArticleBioMed research international2014

Epigenetic control of autophagy by microRNAs in ovarian cancer.

Rossella Titone, Federica Morani, Carlo Follo, Chiara Vidoni, Delia Mezzanzanica, Ciro Isidoro

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 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
3.4field-weighted citation impact, top 7% 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, 32 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Modulation of non-coding RNAs by resveratrol in ovarian cancer cells:Journal of traditional and complementary medicine · 2020
    Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. MicroRNA in Ovarian Biology and Disease.Cold Spring Harbor perspectives in medicine · 2015
    Review
  13. Review
  14. Review
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 2 institutions in 1 country.

Rossella TitoneLaboratory of Molecular Pathology, Department of Health Sciences, Centro di Biotecnologie per la Ricerca Medica Applicata, Università del Piemonte Orientale, Via P. Solaroli 17, 28100 Novara, Italy.ORCID 0000-0002-1528-331X
Federica MoraniLaboratory of Molecular Pathology, Department of Health Sciences, Centro di Biotecnologie per la Ricerca Medica Applicata, Università del Piemonte Orientale, Via P. Solaroli 17, 28100 Novara, Italy.ORCID 0000-0002-4903-6878
Carlo FolloLaboratory of Molecular Pathology, Department of Health Sciences, Centro di Biotecnologie per la Ricerca Medica Applicata, Università del Piemonte Orientale, Via P. Solaroli 17, 28100 Novara, Italy.ORCID 0000-0001-9711-2655
Chiara VidoniLaboratory of Molecular Pathology, Department of Health Sciences, Centro di Biotecnologie per la Ricerca Medica Applicata, Università del Piemonte Orientale, Via P. Solaroli 17, 28100 Novara, Italy.ORCID 0000-0001-9495-2202
Delia MezzanzanicaUnit of Molecular Therapies, Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, 20133 Milan, Italy.
Ciro IsidoroLaboratory of Molecular Pathology, Department of Health Sciences, Centro di Biotecnologie per la Ricerca Medica Applicata, Università del Piemonte Orientale, Via P. Solaroli 17, 28100 Novara, Italy.ORCID 0000-0002-5494-3034
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” · ITFondazione IRCCS Istituto Nazionale dei Tumori · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autophagy is a lysosomal-driven catabolic process that contributes to the preservation of cell homeostasis through the regular elimination of cellular damaged, aged, and redundant molecules and organelles. Autophagy plays dual opposite roles in cancer: on one hand it prevents carcinogenesis; on the other hand it confers an advantage to cancer cells to survive under prohibitive conditions. Autophagy has been implicated in ovarian cancer aggressiveness and in ovarian cancer cell chemoresistance and dormancy. Small noncoding microRNAs (miRNAs) regulate gene expression at posttranscriptional level, thus playing an important role in many aspects of cell pathophysiology, including cancerogenesis and cancer progression. Certain miRNAs have recently emerged as important epigenetic modulators of autophagy in cancer cells. The mRNA of several autophagy-related genes contains, in fact, the target sequence for miRNAs belonging to different families, with either oncosuppressive or oncogenic activities. MiRNA profiling studies have identified some miRNAs aberrantly expressed in ovarian cancer tissues that can impact autophagy. In addition, plasma and stroma cell-derived miRNAs in tumour-bearing patients can regulate the expression of relevant autophagy genes in cancer cells. The present review focuses on the potential implications of miRNAs regulating autophagy in ovarian cancer pathogenesis and progression.

Indexed as

AutophagyEpigenesis, GeneticAnimalsFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsOvarian NeoplasmsRNA, NeoplasmMicroRNAsRNA, Neoplasm

Identifiers

PMID24877083
PMCPMC4022060
OpenAlexW2137163095

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.