Evidence map›Paper›PMID 30710321›Full record

ArticlePathology oncology research : POR2019

Toll-Like Receptor 4 and Matrix Metalloproteases 11 and 13 as Predictors of Tumor Recurrence and Survival in Stage II Colorectal Cancer.

Noemi Eiro, Juan Francisco Carrión, Sandra Cid, Alejandro Andicoechea, José Luis García-Muñiz, Luis O González, Francisco J Vizoso

Abstract read
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In one paragraph

Article in Pathology oncology research : POR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

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  10. Identification of Hub Genes Associated with COPD Through Integrated Bioinformatics Analysis.International journal of chronic obstructive pulmonary disease
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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 1 institution in 1 country.

Noemi EiroUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain.
Juan Francisco CarriónUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain.
Sandra CidUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain.
Alejandro AndicoecheaServicio de Cirugía General, Fundación Hospital de Jove, 33290, Gijón, Asturias, Spain.
José Luis García-MuñizUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain.
Luis O GonzálezUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain.
Francisco J VizosoUnidad de Investigación, Fundación Hospital de Jove, Avda. Eduardo Castro 161, 33290, Gijón, Asturias, Spain. investigacion@hospitaldejove.com.ORCID http://orcid.org/0000-0002-2827-5511
Fundación Hospital de Jove · ES

Funding

Gobierno del Principado de Asturias (ES) GRUPIN14-116
6 · The paper itself

Abstract

Current clinical-pathologic stratification factors do not allow clear identification of high-risk stage II colorectal cancer (CRC) patients. Therefore, the identification of additional prognostic markers is desirable. Toll-like receptor (TLR)-4 is activated during tumorigenesis and matrix metalloproteases (MMPs) are involved in invasion and metastasis. We aimed to evaluate the expression and clinical relevance of TLR4, MMP11 and MMP13 for patients with stage II CRC. Immunohistochemistry was used to study the expression of TLR4, MMP11 and MMP13 in 96 patients with stage II CRC. We measured the global expression and the expression by different cell types (tumor cells, cancer-associated fibroblasts (CAFs) and mononuclear inflammatory cells (MICs)). The potential relationship between expressions of factors and different prognostic variables were evaluated. Our results show significant relationships between either TLR4 expression by tumor cells and MMP11 expression by CAFs and high risk of tumor recurrence. In addition, the concurrence of age ≥ 75 years and the non-expression of MMP11 by CAFs identify a subgroup of patients with a good prognosis. Our results show that TLR4 expression by tumor cells and MMP11 expression by CAFs may to improve the identification of patients with stage II CRC with a high-risk of relapse.

Indexed as

AgedAged, 80 and overBiomarkers, TumorColorectal NeoplasmsFemaleFollow-Up StudiesGene Expression Regulation, NeoplasticHumansMaleMatrix Metalloproteinase 11Matrix Metalloproteinase 13Middle AgedNeoplasm MetastasisNeoplasm Recurrence, LocalNeoplasm StagingPrognosisBiomarkers, TumorMatrix Metalloproteinase 11Matrix Metalloproteinase 13MMP11 protein, humanMMP13 protein, humanTLR4 protein, humanToll-Like Receptor 4MMP11MMP13Prognostic factorStage II colorectal cancerSurvivalTLR4

Identifiers

PMID30710321
OpenAlexW2914398490

What OpenQuestion holds

Textmetadata
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.