Evidence map›Paper›PMID 33888871›Full record

ArticleCancer gene therapy2022

Downregulation of miR-335 exhibited an oncogenic effect via promoting KDM3A/YAP1 networks in clear cell renal cell carcinoma.

Wenqiang Zhang, Ruiyu Liu, Lin Zhang, Chao Wang, Ziyan Dong, Jiasheng Feng, Mayao Luo, Yifan Zhang, Zhuofan Xu, Shidong Lv and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer gene therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

13 citing papers in PubMed, 16 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Wenqiang Zhang *Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Ruiyu Liu *Department of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Lin ZhangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Chao WangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Ziyan DongDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Jiasheng FengDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Mayao LuoDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Yifan ZhangDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Zhuofan XuDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China.
Shidong LvDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China. Lsd990@163.com.
Qiang WeiDepartment of Urology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong, China. qwei@smu.edu.cn.ORCID http://orcid.org/0000-0002-6875-7697
Nanfang Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common type of renal cancer affecting many people worldwide. Although the 5-year survival rate is 65% in localized disease, after metastasis, the survival rate is <10%. Emerging evidence has shown that microRNAs (miRNAs) play a crucial regulatory role in the progression of ccRCC. Here, we show that miR-335, an anti-onco-miRNA, is downregulation in tumor tissue and inhibited ccRCC cell proliferation, invasion, and migration. Our studies further identify the H3K9me1/2 histone demethylase KDM3A as a new miR-335-regulated gene. We show that KDM3A is overexpressed in ccRCC, and its upregulation contributes to the carcinogenesis and metastasis of ccRCC. Moreover, with the overexpression of KDM3A, YAP1 was increased and identified as a direct downstream target of KDM3A. Enrichment of KDM3A demethylase on YAP1 promoter was confirmed by CHIP-qPCR and YAP1 was also found involved in the cell growth and metastasis inhibitory of miR-335. Together, our study establishes a new miR-335/KDM3A/YAP1 regulation axis, which provided new insight and potential targeting of the metastasized ccRCC.

Indexed as

Carcinoma, Renal CellJumonji Domain-Containing Histone DemethylasesKidney NeoplasmsMicroRNAsYAP-Signaling ProteinsCarcinogenesisCell Line, TumorCell ProliferationDown-RegulationGene Expression Regulation, NeoplasticHumansJumonji Domain-Containing Histone DemethylasesKDM3A protein, humanMicroRNAsMIRN335 microRNA, humanYAP1 protein, humanYAP-Signaling Proteins

Identifiers

PMID33888871
PMCPMC9113937
OpenAlexW3152813647

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.