Evidence map›Paper›PMID 30008916›Full record

ArticleOncology letters2018

Oncogenic miR-425-5p is associated with cellular migration, proliferation and apoptosis in renal cell carcinoma.

Jing Quan, Yawen Li, Xiang Pan, Yulin Lai, Tao He, Canbin Lin, Liang Zhou, Liwen Zhao, Shuolei Sun, Yu Ding and 8 more

Abstract read
In one paragraph

Article in Oncology letters, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

  1. Review
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  12. miR-152 inhibits the proliferation and invasion of chordoma cells by targetingThe Journal of international medical research · 2019
    Article
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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

18 authors.

Jing QuanDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Yawen LiDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Xiang PanDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Yulin LaiDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Tao HeDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Canbin LinDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Liang ZhouDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Liwen ZhaoDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Shuolei SunDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Yu DingDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Lingzhi TaoDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Yimin HuDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Xionghui WuDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Zebo ChenDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Fangting ZhangThe Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Institute of Urology of Shenzhen PKU-HKUST Medical Center, Shenzhen, Guangdong 518036, P.R. China.
Jing YeThe Guangdong and Shenzhen Key Laboratory of Male Reproductive Medicine and Genetics, Peking University Shenzhen Hospital, Institute of Urology of Shenzhen PKU-HKUST Medical Center, Shenzhen, Guangdong 518036, P.R. China.
Liangchao NiDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.
Yongqing LaiDepartment of Urology, Peking University Shenzhen Hospital, Shenzhen, Guangdong 518036, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An increasing number of studies have demonstrated the function of microRNAs (miRNAs) in the initiation and development of various types of cancer. Among them, miR-425-5p is proven to serve an important function in several types of cancer, including gastric, cervical cancer, and hepatocellular carcinoma. However, the function of miR-425-5p in renal cell carcinoma (RCC) remains unclear. In the present study, it was demonstrated that the expression level of miR-425-5p was upregulated in RCC tissues and cell lines compared with normal tissues and cell lines (P<0.05). Additionally, Cell Counting kit-8 and MTT assays were employed to assess cell viability and proliferation, whereas wound healing and Transwell assays were employed to examine migration and invasion. The results demonstrated that upregulation of miR-425-5p promoted cell viability and the invasion and migration of ACHN and 786O cells (P<0.05). Flow cytometric analysis confirmed that upregulation of miR-425-5p inhibited apoptosis of ACHN and 786O cells (P<0.05). Downregulation of miR-425-5p inhibited the viability and invasion and migration of ACHN and 786O cells (P<0.05). In the present study, upregulation of miR-425-5p inhibited apoptosis of ACHN and 786O cells whereas no differences in early apoptotic rate were observed between the inhibitor and inhibitor NC groups for 786O and ACHN cells. These results indicate that miR-425-5p may act as an oncogene in RCC.

Indexed as

microRNAmicroRNA-425-5poncogenerenal cell carcinoma

Identifiers

PMID30008916
PMCPMC6036448

What OpenQuestion holds

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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.