Evidence map›Paper›PMID 25519054›Full record

ArticleScientific reports2014

MiR-223-3p targeting SEPT6 promotes the biological behavior of prostate cancer.

Yongbao Wei, Jinrui Yang, Lu Yi, Yinhuai Wang, Zhitao Dong, Ziting Liu, Shifeng Ou-yang, Hongtao Wu, Zhaohui Zhong, Zhuo Yin and 4 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 2 pooled it
3.0field-weighted citation impact, top 9% 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

51 citing papers in PubMed, 2 syntheses or guidelines pooled it, 108 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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  14. Clinical profile inFrontiers in medicine · 2022
    Article
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  17. Observational
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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

14 authors at 2 institutions in 1 country.

Yongbao WeiDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Jinrui YangDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Lu YiDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Yinhuai WangDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhitao DongDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Ziting LiuDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Shifeng Ou-yangDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Hongtao WuDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhaohui ZhongDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhuo YinDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Keqin ZhouDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Yunliang GaoDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Bin YanDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Zhao WangDepartment of Urology, the Second Xiangya Hospital, Central South University, Changsha 410011, China.
Second Xiangya Hospital of Central South University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) present frequently altered expression in urologic cancers including prostate, bladder, and kidney cancer. The altered expression of miR-223 has been reported in cancers and other diseases in recent researches. MiR-223 is up-regulated in systemic lupus erythematosus and rheumatoid arthritis. In neoplastic diseases, miR-223 is proved to be up-expressed in plasma or serum and cancer tissues compared with normal tissues in pancreatic cancer, gastric cancer, et al. However, whether altered expression of miR-223 is associated with prostate cancer (PCa) and what it is potential functions in PCa remained unveiled. In this study, we firstly found miR-223-3p were up-regulated in prostate cancer tissues and then we study functional role of miR-223-3p in PCa using DU145, PC3 and LNCaP cell lines. Our data suggested that miR-223-3p might target gene SEPT6 and promoted the biological behavior of prostate cancer. Notably, we found increasing SEPT6 expression might reverse the biological activity induced by miR-223-3p, which might be a potential therapeutic target for PCa.

Indexed as

Cell Line, TumorGene Expression Regulation, NeoplasticHumansMaleMicroRNAsProstatic NeoplasmsSeptinsUp-RegulationMicroRNAsMIR223, humanSEPTIN6 protein, humanSeptins

Identifiers

PMID25519054
PMCPMC4269886
OpenAlexW1981859869

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.