Evidence map›Paper›PMID 32596959›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2020

The miR-140-5p/KLF9/KCNQ1 axis promotes the progression of renal cell carcinoma.

Chenchen Huang, Jianfa Li, Xiaoting Zhang, Tiefu Xiong, Jing Ye, Jing Yu, Yaoting Gui

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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
1.8field-weighted citation impact, top 15% 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, 32 citations in OpenAlex.

  1. Pooled it
  2. Review
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  11. A Novel Role of Arrhythmia-Related GeneInternational journal of molecular sciences · 2022
    Article
  12. Article
  13. Crucial Roles of miR-625 in Human Cancer.Frontiers in medicine · 2022
    Review
  14. Article
  15. Article
  16. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Chenchen HuangGuangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Jianfa LiGuangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Xiaoting ZhangShenzhen Bao'an District Songgang People's Hospital, Shenzhen, China.
Tiefu XiongGuangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Jing YeGuangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Jing YuDepartment of Laboratory Medicine, Peking University Shenzhen Hospital, Shenzhen, China.
Yaoting GuiGuangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Clinical College of Anhui Medical University, Shenzhen, China.
Anhui Medical University · CNPeking University Shenzhen Hospital · CNShenzhen Bao'an District People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although renal cell carcinoma (RCC) is a common malignant urological cancer, its pathogenesis remains unclear. Previous studies have indicated that miR-140-5p acts as a tumor suppressor in various tumors, including bladder cancer, hepatocellular carcinoma, and gastric cancer, but its biological function in RCC remains unknown. In the present study, we found that miR-140-5p was upregulated in RCC tissues, whereas Krüppel-like factor 9 (KLF9) was downregulated and correlated inversely with miR-140-5p in RCC tissues. miR-140-5p promoted the proliferation, migration, and invasion of RCC cells in vitro, and knockdown of miR-140-5p significantly suppressed tumor growth and lung metastasis in nude mouse model of RCC. We also found that miR-140-5p significantly suppressed the expression of KLF9 by binding to the 3'-UTR of KLF9 mRNA and that KLF9, as a transcription factor, upregulates KCNQ1 (also called K

Indexed as

3' Untranslated RegionsAnimalsCarcinoma, Renal CellCell LineCell Line, TumorCell MovementCell ProliferationDisease ProgressionDown-RegulationFemaleGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHEK293 CellsHumansKCNQ1 Potassium ChannelKidney Neoplasms3' Untranslated RegionsKCNQ1 Potassium ChannelKCNQ1 protein, humanKLF9 protein, humanKruppel-Like Transcription FactorsMicroRNAsMirn140 microRNA, humanKCNQ1KLF9miR-140-5pproliferation/invasion/metastasisrenal cell carcinoma

Identifiers

PMID32596959
OpenAlexW3037678785

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.