Evidence map›Paper›PMID 29861738›Full record

ArticleStem cells international2018

Chronic Inflammation May Enhance Leiomyoma Development by the Involvement of Progenitor Cells.

Monia Orciani, Miriam Caffarini, Alessandra Biagini, Guendalina Lucarini, Giovanni Delli Carpini, Antonella Berretta, Roberto Di Primio, Andrea Ciavattini

Open access · goldAbstract read
In one paragraph

Article in Stem cells international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 2 pooled it
4.2field-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

38 citing papers in PubMed, 2 syntheses or guidelines pooled it, 79 citations in OpenAlex.

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  5. Effects of Adalimumab on Mitochondria of Psoriatic Mesenchymal Stem Cells.Journal of cellular and molecular medicine · 2025
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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

8 authors at 2 institutions in 1 country.

Monia OrcianiDepartment of Clinical and Molecular Sciences and Histology, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0003-4503-3693
Miriam CaffariniDepartment of Clinical and Molecular Sciences and Histology, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0001-7688-420X
Alessandra BiaginiDepartment of Clinical Science, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0002-4580-7401
Guendalina LucariniDepartment of Clinical and Molecular Sciences and Histology, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0003-3218-5620
Giovanni Delli CarpiniDepartment of Clinical Science, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0003-2849-4690
Antonella BerrettaClinic of Immunology, Azienda Ospedali Riuniti di Ancona, 60126 Ancona, Italy.ORCID 0000-0003-4305-1564
Roberto Di PrimioDepartment of Clinical and Molecular Sciences and Histology, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0003-3044-1731
Andrea CiavattiniDepartment of Clinical Science, Università Politecnica delle Marche, 60126 Ancona, Italy.ORCID 0000-0002-8037-4947
Marche Polytechnic University · ITOspedali Riuniti di Ancona · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although the etiology of leiomyoma is unclear, a progenitor/undifferentiated cell population has been described whose dysregulation may be involved in the onset of uterine conditions. Moreover, inflammation is involved in the development of several tumors. The aim of this work was to understand if progenitor cells sustain a chronic inflammatory microenvironment that enhances leiomyoma development. Cells from 12 human leiomyoma and 12 normal myometrium samples of the same patients were in vitro isolated and exhaustively characterized (morphology, proliferation, cytofluorometry, differentiation, RT-PCR, immunofluorescence, immunohistochemistry, and Western blotting assays). Selected cytokines (ELISA) and inflammation-related genes (RT-PCR) were analyzed to identify healthy myometrium progenitor cells (MPCs) and leiomyoma progenitor cells (LPCs). Results show that (i) MPCs and LPCs share stemness features, such as immunophenotype and multidifferentiation assay, (ii) LPCs have a significantly shorter doubling time and a significantly higher expression of stemness genes (

Identifiers

PMID29861738
PMCPMC5971255
OpenAlexW2799383838

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.