Evidence map›Paper›PMID 34289837›Full record

ArticleCancer cell international2021

miR-198 inhibits the progression of renal cell carcinoma by targeting BIRC5.

Chao Yuan, Zhenhong Su, Shengjie Liao, Duanzhuo Li, Zhiwen Zhou, Yawen Wang, Mingchun Quan, Lingling Zeng, Cai Lv, Chenyi Shen and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2021. 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
0.8field-weighted citation impact, top 34% 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, 13 citations in OpenAlex.

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  5. miR-198 targetsFrontiers in oncology · 2024
    Article
  6. Article
  7. Article
  8. The promising role and prognostic value of miR-198 in human diseases.American journal of translational research · 2022
    Article
  9. Article
  10. Article
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

17 authors at 5 institutions in 1 country.

Chao Yuan *Hubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Zhenhong Su *Hubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Shengjie Liao *Hubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Duanzhuo LiHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Zhiwen ZhouHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Yawen WangHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Mingchun QuanHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Lingling ZengHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China.
Cai LvDepartment of Urology, Haikou Municipal Hospital, Haikou, 570208, Hainan, China.
Chenyi ShenYixing Cancer Hospital, Dongshan Dong Lu No. 45, Yixing, 214200, Jiangsu, China.
Weida GongYixing Cancer Hospital, Dongshan Dong Lu No. 45, Yixing, 214200, Jiangsu, China.
Jianfeng WuYixing Cancer Hospital, Dongshan Dong Lu No. 45, Yixing, 214200, Jiangsu, China.
Xiaogang ChenHuangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, 435000, Hubei, China.
Wenbing HuHuangshi Central Hospital, Affiliated Hospital of Hubei Polytechnic University, Huangshi, 435000, Hubei, China.
Xu LvYixing Cancer Hospital, Dongshan Dong Lu No. 45, Yixing, 214200, Jiangsu, China. 64705361@qq.com.
Wenxia SiHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China. 203133@hbpu.edu.cn.ORCID http://orcid.org/0000-0001-9380-7791
Xin YuHubei Key Laboratory for Kidney Disease Pathogenesis and Intervention, Hubei Polytechnic University School of Medicine, Xialu District guilin north, road no. 16, Huangshi, 435003, Hubei, China. yuxin@zqmc.cn.
Hubei Polytechnic University · CNYixing Tumor Hospital · CNHaikou City People's Hospital · CNJiangsu University · CNZhaoqing University · CN

Funding

Huangshi Science and Technology Plan Project 2014A069-1Hubei Nature Science Foundation 2014CFC1094Hubei Polytechnic University School Talent introduction project 18XJZ04RHubei Polytechnic University School Talent introduction project 19XJK06Rnatural science foundation of hubei province 2019CFB184the China National Natural Science Foundation young scholar grant 81902860
6 · The paper itself

Abstract

backgroundmiR-198 is involved in the formation, migration, invasion, and metastasis of various malignant cancers. However, the function and mechanism of action of miR-198 in the tumorigenesis of renal cell carcinoma (RCC) remain elusive. Here, we aimed to explore the role of miR198 in RCC.

methodsImmunohistochemistry was performed to estimate the level of survivin in RCC sections. Quantitative real-time polymerase chain reaction was performed to determine the expression level of miR-198 in fresh RCC tissues. Furthermore, the target relationship between miR-198 and BIRC5 was predicted using the TargetScanHuman 7.2 database and verified via dual-luciferase reporter assay and western blotting. The effects of miR-198 on the viability, apoptosis, invasion, and migration of A498 and ACHN cells were studied using Cell Counting Kit-8, flow cytometry, transwell migration assay, and wound healing assay, respectively. Additionally, a xenograft nude mouse model was established to evaluate the effect of miR-198 on RCC tumorigenesis.

resultsThe expression levels of BIRC5 and miR-198 were respectively higher and lower in RCC tissues than those in normal adjacent tissues. Furthermore, miR-198 could inhibit luciferase activity and reduce the protein level of survivin without affecting the BIRC5 mRNA levels. miR-198 inhibited cell viability, migration, and invasion and promoted cell apoptosis; co-transfection with BIRC5 could rescue these effects. Moreover, miR-198 could repress tumor growth in the xenograft nude mouse model of RCC.

conclusionsOur study demonstrates that miR-198 suppresses RCC progression by targeting BIRC5.

Indexed as

ApoptosisBIRC5/survivinmiR-198Renal cell carcinoma

Identifiers

PMID34289837
PMCPMC8296723
OpenAlexW3184076125

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.