Evidence map›Paper›PMID 32982295›Full record

ArticleOncoTargets and therapy2020

Matrix Metalloproteinase 11 is a Potential Biomarker in Bladder Cancer Diagnosis and Prognosis.

Chen Chen, Xiaoping Liu, Jiazhi Jiang, Shenjuan Li, Gang Wang, Lingao Ju, Fubing Wang, Tongzu Liu, Sheng Li

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 28% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  4. Selected Cytokines and Metalloproteinases in Inflammatory Bowel Disease.International journal of molecular sciences · 2023
    Review
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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

9 authors at 1 institution in 1 country.

Chen ChenDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Xiaoping LiuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Jiazhi JiangDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Shenjuan LiDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Gang WangDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Lingao JuDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.ORCID 0000-0003-0813-3628
Fubing WangDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.ORCID 0000-0002-5971-2622
Tongzu LiuDepartment of Urology, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.
Sheng LiDepartment of Biological Repositories, Zhongnan Hospital of Wuhan University, Wuhan, People's Republic of China.ORCID 0000-0003-4070-7345
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBladder cancer is one of the leading causes of cancer death all over the world, and half of patients are diagnosed at advanced stages with poor therapeutic response. Thus, developing new biomarkers for bladder cancer diagnosis and prognosis is urgently needed. MATERIALS AND

methodsBioinformatic and gene ontology (GO) analysis were employed to screen highly upregulated and secretory tumor markers in the TCGA BLCA cohort. IHC in tissue microarray and ELISA in cancer cell culture medium were used to validate the expression of putative biomarkers in bladder cancer. Bisulfite sequencing was used to detect DNA methylation status in the promoter of putative genes.

resultsIn this study, MMP11 is first identified as one of the most differentially expressed genes (DEGs) in bladder cancer by meta-analysis in a TCGA bladder cancer cohort. The strong upregulation of MMP11 is confirmed at protein levels in both bladder cancer patients and cell lines. Mechanistic studies reveal that MMP11 promoter hypomethylation, but not genomic amplification or mutation, accounts for its enhanced expression in bladder cancer both in vitro and in vivo. Moreover, clinicopathological analysis indicates that MMP11 upregulation is associated with the tumor progression and poor survival in bladder cancer patients. DISCUSSION: These findings suggest that MMP11, as a secretory protein, is a promising biomarker for diagnosis and prognosis in bladder cancer.

Indexed as

bladder cancerDEGdiagnosishypomethylationMMP11prognosisTCGA

Identifiers

PMID32982295
PMCPMC7494396
OpenAlexW3085809856

What OpenQuestion holds

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Registered trials

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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.