Evidence map›Paper›PMID 36411681›Full record

ArticleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences2022

Effect of miRNA-200b on the proliferation of liver cancer cells via targeting SMYD2/p53 signaling pathway.

Weijin Fang, Liying Song, Zuojun Li, Peipei Meng, Shanru Zuo, Shikun Liu

Open access · greenAbstract read
In one paragraph

Article in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 53% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
  3. 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

6 authors at 2 institutions in 1 country.

Weijin FangDepartment of Pharmacy, Third Xiangya Hospital, Central South University, Changsha 410013. Fangweijin03@126.com.
Liying SongDepartment of Pharmacy, Third Xiangya Hospital, Central South University, Changsha 410013.
Zuojun LiDepartment of Pharmacy, Third Xiangya Hospital, Central South University, Changsha 410013.
Peipei MengDepartment of Pharmacy, Women and Children's Health Care Hospital of Linyi, Linyi Shandong 276000, China.
Shanru ZuoDepartment of Pharmacy, Third Xiangya Hospital, Central South University, Changsha 410013.
Shikun LiuDepartment of Pharmacy, Third Xiangya Hospital, Central South University, Changsha 410013. L8618496@126.com.
Third Xiangya Hospital · CNCentral South University · CN

Funding

the Natural Science Foundation of Hunan Province 2018JJ3795
6 · The paper itself

Abstract

objectivesOur previous study has verified that high level of SET and MYND domain-containing protein 2 (SMYD2) plays an important role in acquiring aggressive ability for liver cancer cells in hepatocellular carcinoma. MiR-200b as a tumor suppressor gene involves in a variety of cancers. This study aims to investigate the correlation between miR-200b and SMYD2 in hepatocellular carcinoma and the underlying mechanism.

methodsFirstly, the levels of SMYD2 and miR-200b in hepatocellular carcinoma tissues and matched adjacent non-tumor liver tissues were tested with real-time reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. Secondly, we evaluated the interaction between miR-200b and SMYD2 using dual-luciferase reporter assay. Thirdly, we elucidated the effect of miR-200b on SMYD2 and its downstream targets p53/CyclinE1. Finally, we silenced SMYD2 in hepatocellular carcinoma cell lines to investigate its effect on tumor proliferation and cell cycle progression, and further confirmed the correlation among SMYD2 and p53/CyclinE1.

resultsCompared with the matched adjacent non-tumor liver tissues, miR-200b was obviously decreased, and SMYD2 was significantly increased in hepatocellular carcinoma (both

conclusionsMiR-200b is involved in hepatocellular carcinoma progression via targeting SMYD2 and regulating SMYD2/p53/CyclinE1 signaling pathway and may be used as a potential target for hepatocellular carcinoma treatment.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicroRNAsCell Line, TumorCell ProliferationHistone-Lysine N-MethyltransferaseHumansSignal TransductionTumor Suppressor Protein p53Histone-Lysine N-MethyltransferaseMicroRNAsSMYD2 protein, humanTumor Suppressor Protein p53CyclinE1hepatocellular carcinomamiR-200bp53SET and MYND domain-containing protein 2

Identifiers

PMID36411681
PMCPMC10930361
OpenAlexW4309660864

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.