Evidence map›Paper›PMID 26823729›Full record

ArticleInternational journal of clinical and experimental pathology2015

Expression and functional role of miR-29b in renal cell carcinoma.

Yi Xu, Jianyong Zhu, Zhangming Lei, Lijun Wan, Xiuwen Zhu, Feng Ye, Yanyue Tong

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. MicroRNA Signature in Renal Cell Carcinoma.Frontiers in oncology · 2020
    Review
  6. Serum miR-29b as a novel biomarker for glioblastoma diagnosis and prognosis.International journal of clinical and experimental pathology · 2019
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. 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

7 authors at 1 institution in 1 country.

Yi XuDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Jianyong ZhuDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Zhangming LeiDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Lijun WanDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Xiuwen ZhuDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Feng YeDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Yanyue TongDepartment of Urology, Quzhou People's Hospital Quzhou 324000, Zhejiang, China.
Quzhou City People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesmicroRNAs (miRNAs) play essential roles in many tumors, including renal cell carcinoma (RCC). The aim of the present study was to investigate the expression and functional role of miR-29b in RCC and to identify its target genes.

methodsWe determined the expression of miR-29b in clear cell RCC (ccRCC) tissues and RCC cell lines (786-O, A498, and SN12-PM6) using quantitative real-time PCR (qRT-PCR). The associations between miR-29b expression and clinical pathological parameters and prognosis were explored. Besides, the role of miR-29b in the SN12-PM6 cells proliferation, apoptosis, cycle, and invasion were investigated after transduction with lentivirus vectors. The kines in family member 1B (KIF1B), possible miR-29b target genes, were predicted using bioinformatics approaches, as well as the role in the pathogenesis of RCC.

resultsElevated expression of miR-29b was found in both tumor tissues and cell lines. High expression of miR-29b was significantly associated with tumor-node-metastasis (TNM) stage (P = 0.026) and the overall survival (P = 0.009) in the ccRCC. Inhibition of miR-29b expression could promote apoptosis, and inhibit proliferation and invasion ability in SN12-PM6 cells. Also, we confirmed that miR-29b could directly regulate the expression of KIF1B at the post transcriptional level.

conclusionThese data suggest that miR-29b acts as an oncomiR, promoting proliferation and invasion ability through KIF1B suppression, and it might be a potential marker for prognosis of RCC.

Indexed as

AgedApoptosisCarcinoma, Renal CellCell CycleCell Line, TumorCell MovementCell ProliferationComputational BiologyDatabases, GeneticFemaleGene Expression Regulation, NeoplasticHumansKaplan-Meier EstimateKidney NeoplasmsKinesinsMaleKIF1B protein, humanKinesinsMicroRNAsMIRN29a microRNA, humankinesin family member 1BmiR-29bRenal cell carcinoma

Identifiers

PMID26823729
PMCPMC4713515
OpenAlexW2404103017

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.