Evidence map›Paper›PMID 27909734›Full record

ArticleInternational journal of molecular medicine2017

Klf4 inhibits tumor growth and metastasis by targeting microRNA-31 in human hepatocellular carcinoma.

Chuan Tian, Shanshan Yao, Li Liu, Youcheng Ding, Qingwang Ye, Xiao Dong, Yong Gao, Ning Yang, Qi Li

Open access · hybridAbstract read
In one paragraph

Article in International journal of molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Chuan TianDepartment of Oncology, Shanghai First People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, P.R. China.
Shanshan YaoDepartment of Oncology, Shanghai First People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, P.R. China.
Li LiuDepartment of Pharmacy, Guiyang Hospital of Guizhou Aviation Industry Group, Guiyang, Guizhou, P.R. China.
Youcheng DingDepartment of General Surgery, Shanghai East Hospital, Tongji University, Shanghai, P.R. China.
Qingwang YeDepartment of Liver Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, P.R. China.
Xiao DongDepartment of Oncology, Shanghai First People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, P.R. China.
Yong GaoDepartment of Oncology, Shanghai East Hospital, Tongji University, Shanghai, P.R. China.
Ning YangDepartment of Liver Surgery, Eastern Hepatobiliary Surgery Hospital, Second Military Medical University, Shanghai, P.R. China.
Qi LiDepartment of Oncology, Shanghai First People's Hospital Affiliated to Shanghai Jiaotong University, Shanghai, P.R. China.
Shanghai First People's Hospital · CNEastern Hepatobiliary Surgery Hospital · CNShanghai East Hospital · CNAviation Industry Corporation of China (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs or miRs) are short, endogenous non-coding RNA molecules, demonstrating abnormal expression in cancer initiation and progression. In this study, we profiled 18 differentially regulated miRNAs, including miRNA‑31, using miRNA array. Kruppel (or Krüppel)-like factor 4 (Klf4) is a transcription factor and putative tumor suppressor. Both were found to be significantly downregulated in liver cancer tissues and cells. However, little is known about the correlation between Klf4 and miRNA‑31 in hepatocellular carcinoma (HCC). The mRNA expression of Klf4 was decreased and inversely associated with the clinical stage, T classification and hepatitis B in patients with HCC, while the expression of miR‑31 was lower (r=0.326, P=0.018). Using cell counting kit 8 (CCK8) and Transwell migration assays, we found that Klf4 and miR‑31 inhibited the proliferation and metastasis of liver cancer cells. Moreover, we demonstrated that Klf4 directly binds to the promoter of miR‑31 and activates its transcription. In vitro experiments confirmed that Klf4 regulated miR‑31 and thereby inhibited HCC cell growth and metastasis. Taken together, our findings indicate that Klf4 directly regulates miR‑31 in HCC. Thus, miR-31 may serve as a potential diagnostic marker and therapeutic target in HCC.

Indexed as

Carcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationDown-RegulationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenetic VectorsHumansKruppel-Like Factor 4Kruppel-Like Transcription FactorsLiver NeoplasmsMaleMicroRNAsMiddle AgedKLF4 protein, humanKruppel-Like Factor 4Kruppel-Like Transcription FactorsMicroRNAsMIRN31 microRNA, human

Identifiers

PMID27909734
PMCPMC5179175
OpenAlexW2551182095

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.