Evidence map›Paper›PMID 26743900›Full record

ArticleMolecules and cells2016

miR-101 Inhibiting Cell Proliferation, Migration and Invasion in Hepatocellular Carcinoma through Downregulating Girdin.

Ke Cao, Jingjing Li, Yong Zhao, Qi Wang, Qinghai Zeng, Siqi He, Li Yu, Jianda Zhou, Peiguo Cao

Open access · diamondAbstract read
In one paragraph

Article in Molecules and cells, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

29 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  7. CCDC88A Post-Transcriptionally Regulates VEGFFrontiers in immunology · 2022
    Article
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  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. The Function of the HGF/c-Met Axis in Hepatocellular Carcinoma.Frontiers in cell and developmental biology · 2020
    Review
  17. Article
  18. Article
  19. Article
  20. 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

9 authors at 2 institutions in 1 country.

Ke CaoDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jingjing LiDepartment of Pathology, Xiangya Basic Medical College, Central South University, Changsha, Hunan, China.
Yong ZhaoDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qi WangDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Qinghai ZengDepartment of Plastic Surgery, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Siqi HeDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Li YuDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Jianda ZhouDepartment of Plastic Surgery, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Peiguo CaoDepartment of Oncology, Third Xiangya Hospital, Central South University, Changsha, Hunan, China.
Third Xiangya Hospital · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

miR-101 is considered to play an important role in hepato-cellular carcinoma (HCC), but the underlying molecular mechanism remains to be elucidated. Here, we aimed to confirm whether Girdin is a target gene of miR-101 and determine the tumor suppressor of miR-101 through Girdin pathway. In our previous studies, we firstly found Girdin protein was overexpressed in HCC tissues, and it closely correlated to tumor size, T stage, TNM stage and Edmondson-Steiner stage of HCC patients. After specific small interfering RNA of Girdin was transfected into HepG2 and Huh7.5.1 cells, the proliferation and invasion ability of tumor cells were significantly inhibited. In this study, we further explored the detailed molecular mechanism of Girdin in HCC. Interestingly, we found that miR-101 significantly low-expressed in HCC tissues compared with that in matched normal tissues while Girdin had a relative higher expression, and miR-101 was inversely correlated with Girdin expression. In addition, after miR-101 transfection, the proliferation, migration and invasion abilities of HepG2 cells were weakened. Furthermore, we confirmed that Girdin is a direct target gene of miR-101. Finally we confirmed Talen-mediated Girdin knockout markedly suppressed cell proliferation, migration and invasion in HCC while down-regulation of miR-101 significantly restored the inhibitory effect. Our findings suggested that miR-101/Girdin axis could be a potential application of HCC treatment.

Indexed as

Gene Expression Regulation, NeoplasticBase SequenceCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationHep G2 CellsHumansLiver NeoplasmsMicrofilament ProteinsMicroRNAsMolecular Sequence DataRNA, Small InterferingSignal TransductionVesicular Transport ProteinsCCDC88A protein, humanMicrofilament ProteinsMicroRNAsMIRN101 microRNA, humanRNA, Small InterferingVesicular Transport ProteinsGirdininvasion and metastasismiR-101primary hepatocellular carcinoma cellproliferation

Identifiers

PMID26743900
PMCPMC4757808
OpenAlexW2278365221

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.