Evidence map›Paper›PMID 25115394›Full record

ArticleOncotarget2014

Circulating miR-182 is a biomarker of colorectal adenocarcinoma progression.

Lisa Perilli, Caterina Vicentini, Marco Agostini, Silvia Pizzini, Marco Pizzi, Edoardo D'Angelo, Stefania Bortoluzzi, Susanna Mandruzzato, Enzo Mammano, Massimo Rugge and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 64 citations in OpenAlex.

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  6. miR-182 targeting reprograms tumor-associated macrophages and limits breast cancer progression.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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 4 institutions in 1 country.

Lisa PerilliOncology and Immunology Section, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy; These authors contributed equally to this work.
Caterina VicentiniARC-NET Research Centre, University of Verona, Verona, Italy; These authors contributed equally to this work.
Marco AgostiniDepartment of Surgery, Oncology and Gastroenterology, Surgery Section, University of Padua, Padua, Italy; Istituto di Ricerca Pediatrica - Citta' della Speranza, Padua, Italy.
Silvia PizziniDepartment of Biology, University of Padua, Padua, Italy.
Marco PizziDepartment of Medicine , Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.
Edoardo D'AngeloARC-NET Research Centre, University of Verona, Verona, Italy.
Stefania BortoluzziDepartment of Biology, University of Padua, Padua, Italy.
Susanna MandruzzatoOncology and Immunology Section, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy; Istituto Oncologico Veneto (IOV), IRCCS, Padua, Italy.
Enzo MammanoDepartment of Surgery, Oncology and Gastroenterology, Surgery Section, University of Padua, Padua, Italy.
Massimo RuggeDepartment of Medicine , Surgical Pathology & Cytopathology Unit, University of Padua, Padua, Italy.
Donato NittiDepartment of Surgery, Oncology and Gastroenterology, Surgery Section, University of Padua, Padua, Italy.
Aldo ScarpaARC-NET Research Centre, University of Verona, Verona, Italy; Department of Pathology and Diagnostics, University of Verona, Verona, Italy.
Matteo FassanARC-NET Research Centre, University of Verona, Verona, Italy; Department of Pathology and Diagnostics, University of Verona, Verona, Italy.
Paola ZanovelloOncology and Immunology Section, Department of Surgery, Oncology and Gastroenterology, University of Padua, Padua, Italy; Istituto Oncologico Veneto (IOV), IRCCS, Padua, Italy.
University of Padua · ITUniversity of Verona · ITCittà della Speranza Foundation · ITIstituto Oncologico Veneto · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MiR-182 expression was evaluated by qRT-PCR and in situ hybridization in 20 tubular adenomas, 50 colorectal carcinoma (CRC), and 40 CRC liver metastases. Control samples obtained from patients with irritable bowel syndrome, or tumor-matched normal colon mucosa were analyzed (n=50). MiR-182 expression increased progressively and significantly along with the colorectal carcinogenesis cascade, and in CRC liver metastases. The inverse relation between miR-182 and the expression of its target gene ENTPD5 was investigated by immunohistochemical analysis. We observed that normal colocytes featured a strong ENTPD5 cytoplasmic expression whereas a significantly and progressively lower expression was present along with dedifferentiation of the histologic phenotype. Plasma samples from 51 CRC patients and controls were tested for miR-182 expression. Plasma miR-182 concentrations were significantly higher in CRC patients than in healthy controls or patients with colon polyps at endoscopy. Moreover, miR-182 plasma levels were significantly reduced in post-operative samples after radical hepatic metastasectomy compared to preoperative samples. Our results strengthen the hypothesis of a central role of miR-182 dysregulation in colon mucosa transformation, demonstrate the concomitant progressive down-regulation of ENTPD5 levels during colon carcinogenesis, and indicate the potential of circulating miR-182 as blood based biomarker for screening and monitoring CRC during the follow-up.

Indexed as

AdenocarcinomaAgedBiomarkers, TumorColorectal NeoplasmsDisease ProgressionFemaleHEK293 CellsHumansMaleMicroRNAsOncogene ProteinsPyrophosphatasesTransfectionUp-RegulationBiomarkers, TumorENTPD5 protein, humanMicroRNAsMirn182 microRNA, humanOncogene ProteinsPyrophosphatases

Identifiers

PMID25115394
PMCPMC4196150
OpenAlexW2115981800

What OpenQuestion holds

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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.