Evidence map›Paper›PMID 32678046›Full record

ArticleJournal of translational medicine2020

microRNA-128 mediates CB1 expression and regulates NF-KB/p-JNK axis to influence the occurrence of diabetic bladder disease.

Xin Gou, Jing Wu, Mingqing Huang, Yuting Weng, Tongxin Yang, Tao Chen, Guiqing Li, Kewei Fang

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Journal of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 55% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Xin Gou *Department of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China.
Jing Wu *Department of Biochemistry and Molecular Biology, The Primary Medicine School of Kunming Medical University, Kunming, 650101, People's Republic of China.
Mingqing HuangDepartment of Urology, The 2nd Hospital of Kunming Medical University, Kunming, 650101, People's Republic of China.
Yuting WengDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China.
Tongxin YangDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China.
Tao ChenDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China.
Guiqing LiDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China.
Kewei FangDepartment of Urology, The Second Affiliated Hospital of Kunming Medical University, No. 374, Dianmian Dadao, Kunming, Yunnan, 650101, People's Republic of China. 2482099228@qq.com.
Kunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDiabetic bladder disease is common complications of diabetes, its symptoms are diverse, can be due to different stages. In this study we investigate the mechanism of miR-128 targeting CB1 expression to mediate the occurrence of diabetic bladder disease.

methodsBioinformatics analysis predicts related regulatory factors of miR-128 in diabetic bladder disease. Models of diabetic bladder lesions were constructed in male SD rats by intraperitoneal injection of streptozotocin at 65 mg/kg body weight. The expression of miR-128 and CB1 mRNA in bladder tissues of each group was detected by RT-qPCR, and CB1, NF-KB, p-JNK and Bcl2 protein expression was detected by Western Blotting. We tested the function of the bladder by urodynamics, detected the pathological characteristics of the bladder tissue by HE staining, and verified the targeting relationship between miR-128 and CB1 through the prediction of the biological website, dual luciferase reporter gene assay and RIP.

resultsmiR-128 was highly expressed in the bladder tissue of diabetic rats. Inhibition of miR-128 could improve the occurrence of diabetic bladder lesions in rats. miR-128 could target the inhibition of CB1 expression, and high expression of CB1 could antagonize miR-128 against diabetic bladder. In the diabetic bladder, miR-128 can regulate the expression of NF-KB and p-JNK through CB1 and affect the level of apoptosis. miR-128 regulates NF-KB/p-JNK through CB1, thus affecting the occurrence of diabetic bladder disease.

conclusionThe high expression of miR-128 can down-regulate the expression of CB1, promote the activation of NF-KB and p-JNK, increase the level of apoptosis and promote the occurrence of diabetic bladder disease.

Indexed as

Diabetes Mellitus, ExperimentalMicroRNAsReceptor, Cannabinoid, CB1Urinary Bladder DiseasesAnimalsApoptosisMaleNF-kappa BRatsRats, Sprague-DawleySignal TransductionCnr1 protein, ratMicroRNAsMIRN128 microRNA, ratNF-kappa BReceptor, Cannabinoid, CB1ApoptosisBladder diseaseCB1DiabetesmicroRNA-128NF-KBP-JNK

Identifiers

PMID32678046
PMCPMC7367232
OpenAlexW3165501729

What OpenQuestion holds

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LicenceCC BY
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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.