Evidence map›Paper›PMID 27821157›Full record

ArticleBMC cancer2016

Let-7 inhibits self-renewal of hepatocellular cancer stem-like cells through regulating the epithelial-mesenchymal transition and the Wnt signaling pathway.

Bin Jin, Wei Wang, Xiang-Xin Meng, Gang Du, Jia Li, Shi-Zhe Zhang, Bing-Hai Zhou, Zhi-Hao Fu

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 3% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 100 citations in OpenAlex.

  1. Pooled it
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  5. Cerebrovascular and Peripheral Vascular Complications in Cancer Patients.Current neurology and neuroscience reports · 2025
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  7. Mechanisms of apoptosis-related non-coding RNAs in ovarian cancer: a narrative review.Apoptosis : an international journal on programmed cell death · 2025
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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

8 authors at 3 institutions in 1 country.

Bin JinDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China. prof_binjin@163.com.
Wei WangDepartment of Biochemistry and Molecular Biology, School of Medicine, Shandong University, Jinan, Shandong Province, 250012, China.
Xiang-Xin MengDepartment of General Surgery, The People's Hospital of LingCheng, Dezhou, 253500, China.
Gang DuDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China.
Jia LiDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China.
Shi-Zhe ZhangDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China.
Bing-Hai ZhouDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China.
Zhi-Hao FuDepartment of General Surgery, Qilu Hospital of Shandong University, 107 Wenhua West Road, Lixia District, Jinan, Shandong Province, 250012, China.
Qilu Hospital of Shandong University · CNShandong University · CNZoucheng People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor suppressive let-7 miRNAs are universally down-regulated in human hepatocellular carcinoma (HCC) versus normal tissues; however, the roles and related molecular mechanisms of let-7 in HCC stem cells are poorly understood.

methodsWe examined the inhibitory effect of let-7 miRNAs on the proliferation of MHCC97-H and HCCLM3 hepatic cancer cells by using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay, which was further confirmed by apoptosis and cell cycle studies. The sphere-forming assay was used to study the effects of let-7a on stem like cells. Through western blot, immunofluorescence and the luciferase-reporter assay, we explored the activity of epithelial-mesenchymal transition (EMT) signaling factors in HCC cells. qRT-PCR was applied to detect miRNA expression levels in clinical tissues.

resultsLet-7a effectively repressed cell proliferation and viability, and in stem-like cells, also let-7a decreased the efficiency of sphere formation.in stem-like cells. The suppression of EMT signaling factors in HCC cells contributed to let-7's induced tumor viability repression and Wnt activation repression. Besides, Wnt1 is critical and essential for let-7a functions, and the rescue with recombinant Wnt1 agent abolished the suppressive roles of let-7a on hepatospheres. In clinical HCC and normal tissues, let-7a expression was inversely correlated with Wnt1 expression.

conclusionsLet-7 miRNAs, especially let-7a, will be a promising therapeutic strategy in the treatment of HCC through eliminating HCC stem cells, which could be achieved by their inhibitory effect on the Wnt signaling pathway.

Indexed as

Wnt Signaling PathwayApoptosisCarcinoma, HepatocellularCell CycleCell Line, TumorCell Self RenewalCell Transformation, NeoplasticDisease ProgressionEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHumansLiver NeoplasmsMicroRNAsNeoplastic Stem CellsPlatinumRNA InterferenceMicroRNAsmirnlet7 microRNA, humanPlatinumWnt1 ProteinWNT1 protein, humanCancer stem-like cellsEMTHepatocellular carcinomaLet-7 miRNAsWnt signaling

Identifiers

PMID27821157
PMCPMC5100284
OpenAlexW2552802473

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.