Evidence map›Paper›PMID 31938095›Full record

ArticleInternational journal of clinical and experimental pathology2018

The putative tumour suppressor microRNA-145, repressed by c-jun, modulates clear cell renal cell carcinoma aggressiveness by repressing ROCK1.

Zhen Ding, Xiao Zhang, Zhu Qiao, Hui Li, Qi Ma, Xiaowei Liu, Shangwei Ding

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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.

Zhen DingDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Xiao ZhangDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Zhu QiaoDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Hui LiDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Qi MaDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Xiaowei LiuDepartment of Oncology, Affiliated Hospital of Jining Medical University Jining 272029, Shandong, China.
Shangwei DingDepartment of Ultrasound, Dongguan People's Hospital Affiliated to Southern Medical University Dongguan 523059, Guangdong, China.
Affiliated Hospital of Jining Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aberrant expression of miR-145 has frequently been reported in cancer studies; however, its role in renal cell carcinoma (RCC) has not been examined in detail. Here, we showed that miR-145 was downregulated in RCC cells and tissues and associated with a poor prognostic phenotype in RCC patients. Restoration of miR-145 suppressed proliferation and invasion and induced apoptosis in clear cell RCC (ccRCC) cells. By luciferase and western blot assays we identified ROCK1 as a direct target gene for miR-145. Furthermore, a reverse correlation between miR-145 and ROCK1 expression was observed in ccRCC tissues. In addition, we revealed that miR-145 down-regulation in ccRCC cells was due to EZH2-mediated histone methylation. Altogether, these results identify a crucial tumor suppressive role of miR-145 in the progression of ccRCC and suggest that miR-145 might be an anticancer therapeutic target for ccRCC patients.

Indexed as

A498c-junClear cell renal cell carcinomamiR-145ROCK1

Identifiers

PMID31938095
PMCPMC6957973
OpenAlexW3026631599

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.