Evidence map›Paper›PMID 31886121›Full record

ReviewAnalytical cellular pathology (Amsterdam)2019

The Role of Matrix Metalloproteinases in the Epithelial-Mesenchymal Transition of Hepatocellular Carcinoma.

Cristian Scheau, Ioana Anca Badarau, Raluca Costache, Constantin Caruntu, Gratiela Livia Mihai, Andreea Cristiana Didilescu, Carolina Constantin, Monica Neagu

Open access · goldAbstract readReview
In one paragraph

Review in Analytical cellular pathology (Amsterdam), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 228 papers.

0numbers the graph read from it
0cells of the map it votes in
228citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

228 citing papers in PubMed, 359 citations in OpenAlex.

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  7. Clinical prognostic prediction ofTranslational cancer research · 2026
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  14. Targeting PLK1 Reduces MMP10 to Enhance Radiosensitivity in HPV- Head and Neck Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
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168 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

8 authors at 3 institutions in 1 country.

Cristian ScheauDepartment of Physiology, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.
Ioana Anca BadarauDepartment of Physiology, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.
Raluca CostacheGastroenterology and Internal Medicine Clinic, Carol Davila University Central Emergency Military Hospital, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.ORCID https://orcid.org/0000-0002-0381-5550
Constantin CaruntuDepartment of Physiology, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.ORCID https://orcid.org/0000-0003-4530-7965
Gratiela Livia MihaiDepartment of Physiology, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.
Andreea Cristiana DidilescuDepartment of Embryology, Faculty of Dental Medicine, Carol Davila University of Medicine and Pharmacy, Bucharest 050474, Romania.
Carolina ConstantinImmunology Department, Victor Babes National Institute of Pathology, Bucharest 050096, Romania.ORCID https://orcid.org/0000-0002-2870-5497
Monica NeaguImmunology Department, Victor Babes National Institute of Pathology, Bucharest 050096, Romania.ORCID https://orcid.org/0000-0001-9339-2805
Carol Davila University of Medicine and Pharmacy · ROInstitutul National Victor Babes · ROUniversity of Bucharest · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The epithelial-mesenchymal transition (EMT) is a transformation process mandatory for the local and distant progression of many malignant tumors, including hepatocellular carcinoma (HCC). Matrix metalloproteinases (MMPs) play significant roles in cellular regeneration, programmed death, angiogenesis, and many other essential tissular functions, involved in the normal development and also in pathological processes, such as the EMT. This paper reviews the roles of MMPs in the EMT involved in HCC invasion, as well as the ancillary roles that MMP cross-activation and tissue inhibitors play in modulating this process. While gelatinases MMP-2 and MMP-9 are the MMPs commonly cited in the EMT of HCC, MMPs belonging to other classes have been proven to be involved in this process, favoring not only invasion and metastasis (MMP-1, MMP-3, MMP-7, MMP-10, MMP-11, MMP-13, MMP-14, MMP-16, MMP-26, and MMP-28) but also angiogenesis (MMP-8 and MMP-10). There is also data suggesting that other MMPs with a suspected or demonstrated role in the EMT of other cancers may also have some degree of involvement in HCC. The auto- and cross-activation of MMPs may complicate this issue, as pinpointing the extent of implication of each MMP may be extremely difficult. The homeostasis between MMPs and their tissue inhibitors is essential in preventing tumor progression, and the disturbance of this stability is another entailed factor in the EMT of HCC, which is addressed herein.

Indexed as

Epithelial-Mesenchymal TransitionCarcinogenesisCarcinoma, HepatocellularHumansLiver NeoplasmsMatrix MetalloproteinasesModels, BiologicalMatrix Metalloproteinases

Identifiers

PMID31886121
PMCPMC6899323
OpenAlexW2991029237

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.