Evidence map›Paper›PMID 37511503›Full record

ReviewInternational journal of molecular sciences2023

Multiple Roles of LOXL2 in the Progression of Hepatocellular Carcinoma and Its Potential for Therapeutic Targeting.

Jelena Radić, Bojana Kožik, Ivan Nikolić, Ivana Kolarov-Bjelobrk, Tijana Vasiljević, Bojana Vranjković, Sanja Despotović

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
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  11. Loss of phosphatase and tensin homolog (Cancer pathogenesis and therapy · 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

7 authors at 3 institutions in 1 country.

Jelena RadićFaculty of Medicine, University of Novi Sad, 21137 Novi Sad, Serbia.ORCID 0000-0001-9721-7414
Bojana KožikLaboratory for Radiobiology and Molecular Genetics, Vinča Institute of Nuclear Sciences-National Institute of the Republic of Serbia, University of Belgrade, 11100 Belgrade, Serbia.ORCID 0000-0002-2983-4151
Ivan NikolićFaculty of Medicine, University of Novi Sad, 21137 Novi Sad, Serbia.
Ivana Kolarov-BjelobrkFaculty of Medicine, University of Novi Sad, 21137 Novi Sad, Serbia.ORCID 0000-0003-1239-4994
Tijana VasiljevićFaculty of Medicine, University of Novi Sad, 21137 Novi Sad, Serbia.
Bojana VranjkovićDepartment of Medical Oncology, Oncology Institute of Vojvodina, 21204 Sremska Kamenica, Serbia.
Sanja DespotovićInstitute of Histology and Embryology, Faculty of Medicine, University of Belgrade, 11000 Belgrade, Serbia.
University of Novi Sad · RSUniversity of Belgrade · RSOncology Institute of Vojvodina · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LOXL2, a copper-dependent amine oxidase, has emerged as a promising therapeutic target in hepatocellular carcinoma (HCC). Increased LOXL2 expression in HCC has been linked with an aggressive phenotype and represents a poor prognostic factor. Here, we focus on the mechanisms through which LOXL2 orchestrates multiple oncogenic functions in HCC development. We performed a review of the current knowledge on the roles LOXL2 performs in the modulation of the HCC tumor microenvironment, formation of premetastatic niches, and epithelial-mesenchymal transition. We also highlighted the complex interplay between LOXL2 and hypoxia, angiogenesis, and vasculogenic mimicry in HCC. At the end of the review, we summarize the current LOXL2 inhibitors and discuss their potential in HCC precision treatment.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAmino Acid OxidoreductasesEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansMorphogenesisPhenotypeTumor MicroenvironmentAmino Acid OxidoreductasesLOXL2 protein, humanextracellular matrix (ECM)hepatocellular carcinoma (HCC)LOXL2LOXL2 inhibitorstarget therapytumor microenvironment (TME)

Identifiers

PMID37511503
PMCPMC10380739
OpenAlexW4385202582

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.