Evidence map›Paper›PMID 28717923›Full record

ArticleMolecular and cellular biochemistry2018

MiRNA-200a induce cell apoptosis in renal cell carcinoma by directly targeting SIRT1.

Hao Fu, Wenke Song, Xuancai Chen, Tao Guo, Bin Duan, Xinxi Wang, Yachun Tang, Liang Huang, Chi Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular and cellular biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Observational
  5. Review
  6. Article
  7. Article
  8. Article
  9. miR-566 expression and immune changes in patients with intracranial aneurysm.International journal of clinical and experimental pathology · 2020
    Article
  10. Aging, Melatonin, and the Pro- and Anti-Inflammatory Networks.International journal of molecular sciences · 2019
    Review
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.

Hao FuDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Wenke SongDepartment of Obstetrics and Gynecology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Xuancai ChenDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Tao GuoDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Bin DuanDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Xinxi WangDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Yachun TangDepartment of Urology, Affiliated Nanhua Hospital, University of South China, Hengyang, 421002, Hunan, People's Republic of China.
Liang HuangDepartment of Operative Surgery, School of Medicine, University of South China, Hengyang, 421002, Hunan, People's Republic of China. huangliang0530@hotmail.com.
Chi ZhangDepartment of Pathophisiology, Function Laboratory Center, School of Medicine, University of South China, Hengyang, 421002, Hunan, People's Republic of China. zhangchi9966@hotmail.com.
University of South China · CN

Funding

National Natural Science Foundation of China 81100106Scientific Research Fund of Hunan Provincial Education Department 14C0993
6 · The paper itself

Abstract

Accumulating evidence indicates that microRNAs are implicated in tumor initiation and progression through negatively regulating oncogenes or tumor suppressor genes. In the present study, we report that the expression of miR-200a was significantly lower in renal cell carcinoma (RCC) specimens and RCC cell lines. Restoration of miR-200a suppressed cell growth, arrested cell cycle progression, and promoted cell apoptosis in RCC cell lines. We next used qRT-PCR array technology to identify Sirtuin 1 (SIRT1) as one of the downregulated proteins during miR-200a overexpression in 786-O cells. Following a further assay by luciferase reporter system, SIRT1 was validated as a direct target of miR-200a. Moreover, siRNA-mediated knockdown of SIRT1 could partially phenocopy the effects of miR-200a overexpression. In contrast, overexpression of truncated SIRT1 (without an endogenous 3'-UTR) could rescue the effect of miR-200a overexpression on 786-O cells, which suggested that SIRT1 3'-UTR is targeted by miR-200a specifically. These observations provide further evidence for a critical tumor-suppressive role of the miR-200a in RCC in addition to identifying a novel regulatory mechanism, which may contribute to SIRT1 upregulation in RCC.

Indexed as

ApoptosisCarcinoma, Renal CellFemaleHumansKidney NeoplasmsMaleMicroRNAsNeoplasm ProteinsRNA, NeoplasmSirtuin 1MicroRNAsMIRN200 microRNA, humanNeoplasm ProteinsRNA, NeoplasmSIRT1 protein, humanSirtuin 1ApoptosisMiR-200aRenal cell carcinomaSIRT1

Identifiers

PMID28717923
OpenAlexW2735780224

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.