Evidence map›Paper›PMID 31090157›Full record

ArticleInternational journal of experimental pathology2019

Co-expression of TLR-9 and MMP-13 is associated with the degree of tumour differentiation in prostate cancer.

Elham Kalantari, Maryam Abolhasani, Raheleh Roudi, Mohammad M Farajollahi, Seif Farhad, Zahra Madjd, Shaghayegh Askarian-Amiri, Monireh Mohsenzadegan

Open access · greenAbstract readEvaluation Study
In one paragraph

Article in International journal of experimental pathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.8field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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  14. MiRNA505/NET1 Axis Acts as a CD8OncoTargets and therapy · 2020
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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 1 institution in 1 country.

Elham KalantariOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Maryam AbolhasaniDepartment of Pathology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Raheleh RoudiOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Mohammad M FarajollahiDepartment of Medical Biotechnology, Faculty of Allied Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Seif FarhadDepartment of Immunology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Zahra MadjdOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Shaghayegh Askarian-AmiriPhysiology Research Center and Department of Physiology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Monireh MohsenzadeganDepartment of Medical Laboratory Science, Faculty of Allied Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-2434-9728
Iran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In vitro experiments demonstrated that stimulation of Toll-like receptor 9 (TLR-9) by synthetic TLR-9 ligands induces the invasion of TLR-9-expressing prostate cancer cells through matrix metalloproteinase 13 (MMP-13). However, the clinical value of TLR-9 and MMP-13 co-expression in the pathophysiology of the prostate is unknown. In the study, we evaluated the expression levels and clinical significance of the TLR-9 and MMP-13 in a series of prostate tissues. One hundred and eighty prostate tissues including prostate cancer (PCa) (n = 137), high-grade prostatic intraepithelial neoplasia (HPIN) (n = 18) and benign prostatic hyperplasia (BPH) (n = 25) were immunostained for the TLR-9 and MMP-13 markers. Subsequently, the correlation between the TLR-9 and MMP-13 staining scores and clinicopathological parameters was obtained. Higher expressions of TLR-9 and MMP-13 were found in PCa and high-grade prostatic intraepithelial neoplasia compared to benign prostatic hyperplasia tissues. Among PCa samples, a positive relationship was revealed between the MMP-13 expression and Gleason score (P < 0.001). There was a significant correlation between TLR-9 expression and regional lymph node involvement (P = 0.04). The expression patterns of TLR-9 and MMP-13 markers demonstrated a reciprocal significant correlation between the two markers in the same series of prostate samples (P < 0.001). Furthermore, the Gleason score of TLR-9

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBiopsyCell DifferentiationHumansLymphatic MetastasisMaleMatrix Metalloproteinase 13Middle AgedNeoplasm GradingNeoplasm ProteinsProstatic HyperplasiaProstatic Intraepithelial NeoplasiaProstatic NeoplasmsBiomarkers, TumorMatrix Metalloproteinase 13MMP13 protein, humanNeoplasm ProteinsTLR9 protein, humanToll-Like Receptor 9benign prostatic hyperplasiahigh-grade prostatic intraepithelial neoplasiaMMP-13prostate cancerTLR-9

Identifiers

PMID31090157
PMCPMC6540662
OpenAlexW2944846825

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.