Evidence map›Paper›PMID 29126102›Full record

ArticleCarcinogenesis2018

MiRNA-513a-5p inhibits progesterone receptor expression and constitutes a risk factor for breast cancer: the hOrmone and Diet in the ETiology of breast cancer prospective study.

Paola Muti, Sara Donzelli, Andrea Sacconi, Ahmed Hossain, Federica Ganci, Tania Frixa, Sabina Sieri, Vittorio Krogh, Franco Berrino, Francesca Biagioni and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Carcinogenesis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 24% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
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  13. The circular RNA circCRIM1 inhibits osteosarcoma progression through sponging miR-513.Mammalian genome : official journal of the International Mammalian Genome Society · 2021
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  15. ChrXq27.3 miRNA cluster functions in cancer development.Journal of experimental & clinical cancer research : CR · 2021
    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

14 authors at 5 institutions in 4 countries.

Paola MutiDepartment of Oncology, Faculty of Health Science, McMaster University, Hamilton, ON, Canada.
Sara DonzelliOncogenomic and Epigenetic Unit, Regina Elena Italian National Cancer Institute, Rome, Italy.
Andrea SacconiOncogenomic and Epigenetic Unit, Regina Elena Italian National Cancer Institute, Rome, Italy.
Ahmed HossainThe Statistics for Integrative Genomics and Methods Advancement Laboratory, Population Genomics Program, Department of Clinical Epidemiology and Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Federica GanciOncogenomic and Epigenetic Unit, Regina Elena Italian National Cancer Institute, Rome, Italy.
Tania FrixaOncogenomic and Epigenetic Unit, Regina Elena Italian National Cancer Institute, Rome, Italy.
Sabina SieriDepartment of Preventive and Predictive Medicine, Fondazione Istituto Nazionale Tumori, Milano, Italy.
Vittorio KroghDepartment of Preventive and Predictive Medicine, Fondazione Istituto Nazionale Tumori, Milano, Italy.
Franco BerrinoDepartment of Preventive and Predictive Medicine, Fondazione Istituto Nazionale Tumori, Milano, Italy.
Francesca BiagioniOncogenomic and Epigenetic Unit, Regina Elena Italian National Cancer Institute, Rome, Italy.
Sabrina StranoDepartment of Oncology, Faculty of Health Science, McMaster University, Hamilton, ON, Canada.
Joseph BeyeneThe Statistics for Integrative Genomics and Methods Advancement Laboratory, Population Genomics Program, Department of Clinical Epidemiology and Biostatistics, Faculty of Health Sciences, McMaster University, Hamilton, ON, Canada.
Yosef YardenDepartment of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
Giovanni BlandinoDepartment of Oncology, Faculty of Health Science, McMaster University, Hamilton, ON, Canada.
National Cancer Institute · MYFondazione IRCCS Istituto Nazionale dei Tumori · ITMcMaster University · CAPopulation Health Research Institute · CAWeizmann Institute of Science · IL

Funding

Endogenous Hormones and Premenopausal Breast Cancer RiskR01CA098344 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI MUTI, PAOLA C · 2004 to 2006
$1.5M
NCI NIH HHS R01 CA098344
6 · The paper itself

Abstract

MicroRNAs (miRNAs) might be considered both predictors and players of cancer development. The aim of the present report was to investigate whether many years before the diagnosis of breast cancer miRNA expression is already disregulated. In order to test this hypothesis, we compared miRNAs extracted from leukocytes in healthy women who later developed breast cancer and in women who remain healthy during the whole 15-year follow-up time. Accordantly, we used a case-control study design nested in the hOrmone and Diet in the ETiology of breast cancer (ORDET) prospective cohort study addressing the possibility that miRNAs can serve as both early biomarkers and components of the hormonal etiological pathways leading to breast cancer development in premenopausal women. We compared leukocyte miRNA profiles of 191 incident premenopausal breast cancer cases and profiles of 191 women who remained healthy over a follow-up period of 20 years. The analysis identified 20 differentially expressed miRNAs in women candidate to develop breast cancer versus control women. The upregulated miRNAs, miR-513-a-5p, miR-513b-5p and miR-513c-5p were among the most significantly deregulated miRNAs. In multivariate analysis, miR-513a-5p upregulation was directly and statistically significant associated with breast cancer risk (OR = 1.69; 95% CI 1.08-2.64; P = 0.0293). In addition, the upregulation of miR-513-a-5p displayed the strongest direct association with serum progesterone and testosterone levels. The experimental data corroborated the inhibitory function of miR-513a-5p on progesterone receptor expression confirming that progesterone receptor is a target of miR-513a-5p. The identification of upregulated miR-513a-5p with its oncogenic potential further validates the use of miRNAs as long-term biomarker of breast cancer risk.

Indexed as

AdultAgedBiomarkers, TumorBreast NeoplasmsCase-Control StudiesCohort StudiesEarly Detection of CancerFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsMiddle AgedProspective StudiesReceptors, ProgesteroneRisk FactorsBiomarkers, TumorMicroRNAsMIRN513A1 microRNA, humanReceptors, Progesterone

Identifiers

PMID29126102
PMCPMC6454510
OpenAlexW2766835007

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.