Evidence map›Paper›PMID 25885552›Full record

ArticleBMC cancer2015

Remodeling of extracellular matrix by normal and tumor-associated fibroblasts promotes cervical cancer progression.

Alexandra Fullár, József Dudás, Lászlóné Oláh, Péter Hollósi, Zoltán Papp, Gábor Sobel, Katalin Karászi, Sándor Paku, Kornélia Baghy, Ilona Kovalszky

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 1 pooled it
6.5field-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

92 citing papers in PubMed, 1 synthesis or guideline pooled it, 139 citations in OpenAlex.

  1. Pooled it
  2. Therapy resistance-related ncRNAs in cervical cancer: biomarkers and therapeutic targets.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2026
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32 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 3 countries.

Alexandra Fullár1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. fullarsz@gmail.com.
József DudásDepartment of Otorhinolaryngology, Medical University Innsbruck, Innsbruck, Austria. jozsef.dudas@i-med.ac.at.
Lászlóné Oláh1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. julcsi@korb1.sote.hu.
Péter Hollósi1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. phollosi@yahoo.com.
Zoltán PappMaternity Private Department Kútvölgyi Clinical Block, Semmelweis University, Budapest, Hungary. maternity@maternity.hu.
Gábor Sobel2nd Department of Obstetrics and Gynecology, Semmelweis University, Budapest, Hungary. gabor@sobel.hu.
Katalin KarásziCRUK/MRC Oxford Institute for Radiation Oncology, Department of Oncology, University of Oxford, Oxford, UK. katalin.karaszi@nds.ox.ac.uk.
Sándor Paku1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. paku@korb1.sote.hu.
Kornélia Baghy1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. kori@korb1.sote.hu.
Ilona Kovalszky1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary. koval@korb1.sote.hu.
Semmelweis University · HUHungarian Academy of Sciences · HUInnsbruck Medical University · ATUniversity of Oxford · GB

Funding

Austrian Science Fund FWF P 22287Austrian Science Fund FWF P 25869
6 · The paper itself

Abstract

backgroundComparison of tissue microarray results of 29 cervical cancer and 27 normal cervix tissue samples using immunohistochemistry revealed considerable reorganization of the fibrillar stroma of these tumors. Preliminary densitometry analysis of laminin-1, α-smooth muscle actin (SMA) and fibronectin immunostaining demonstrated 3.8-fold upregulation of laminin-1 and 5.2-fold increase of SMA in the interstitial stroma, indicating that these proteins and the activated fibroblasts play important role in the pathogenesis of cervical cancer. In the present work we investigated the role of normal and tumor-associated fibroblasts.

methodsIn vitro models were used to throw light on the multifactorial process of tumor-stroma interaction, by means of studying the cooperation between tumor cells and fibroblasts. Fibroblasts from normal cervix and cervical cancers were grown either separately or in co-culture with CSCC7 cervical cancer cell line. Changes manifest in secreted glycoproteins, integrins and matrix metallo-proteases (MMPs) were explored.

resultsWhile normal fibroblasts produced components of interstitial matrix and TGF-β1 that promoted cell proliferation, cancer-associated fibroblasts (CAFs) synthesized ample amounts of laminin-1. The following results support the significance of laminin-1 in the invasion of CSCC7 cells: 1.) Tumor-associated fibroblasts produced more laminin-1 and less components of fibrillar ECM than normal cells; 2.) The production of laminin chains was further increased when CSCC7 cells were grown in co-culture with fibroblasts; 3.) CSCC7 cells were capable of increasing their laminin production; 4.) Tumor cells predominantly expressed integrin α6β4 laminin receptors and migrated towards laminin. The integrin profile of both normal and tumor-associated fibroblasts was similar, expressing receptors for fibronectin, vitronectin and osteopontin. MMP-7 secreted by CSCC7 cells was upregulated by the presence of normal fibroblasts, whereas MMP-2 produced mainly by fibroblasts was activated in the presence of CSCC7 cells.

conclusionsOur results indicate that in addition to degradation of the basement membrane, invasion of cervical cancer is accomplished by the remodeling of the interstitial stroma, which process includes decrease and partial replacement of fibronectin and collagens by a laminin-rich matrix.

Indexed as

ActinsAdultAgedBasement MembraneCarcinogenesisCell ProliferationCoculture TechniquesExtracellular MatrixFemaleFibroblastsFibronectinsGene Expression Regulation, NeoplasticHumansIntegrinsLamininMiddle AgedActinsFibronectinsIntegrinsLamininlaminin 1Transforming Growth Factor beta1

Identifiers

PMID25885552
PMCPMC4409756
OpenAlexW2074402761

What OpenQuestion holds

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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.