Evidence map›Paper›PMID 30450735›Full record

ArticleJournal of cellular and molecular medicine2019

TSG101 promotes the proliferation, migration and invasion of hepatocellular carcinoma cells by regulating the PEG10.

Zhiyi Liu, Zilu Tian, Kuan Cao, Bin Zhang, Quan Wen, Xinyu Zhou, Weibin Yang, Tao Wang, Hengliang Shi, Renhao Wang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

21 citing papers in PubMed, 26 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

10 authors at 1 institution in 1 country.

Zhiyi LiuInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Zilu TianInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Kuan CaoInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Bin ZhangInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Quan WenInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xinyu ZhouThe Graduate School, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Weibin YangInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Tao WangInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Hengliang ShiInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.ORCID 0000-0002-9649-1910
Renhao WangInstitute of Digestive Diseases, Xuzhou Medical University, Xuzhou, Jiangsu, China.
Xuzhou Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tumour susceptibility gene 101 (TSG101) is reported to play important roles in the development and progression of several human cancers. However, its potential roles and underlined mechanisms in human hepatocellular carcinoma (HCC) are still needed to be further clarified. In the present study, we reported that knock down of TSG101 suppressed the proliferation, migration and invasion of HCC cells, while overexpression of TSG101 facilitated them. Molecularly, the results revealed that knock down of TSG101 significantly decreased the cell cycle related regulatory factor p53 and p21. In another point, knock down of TSG101 also obviously decreased the level of metallopeptidase inhibitor TIMP1 (Tissue inhibitors of metalloproteinases 1), which results in inhibition of MMP2, MMP7 and MMP9. In contrast, overexpression of TSG101 had opposite effects. The iTRAQ proteomics analysis identified that oncogenic protein PEG10 (Paternally expressed gene 10) might be a potential downstream target of TSG101. Further investigation showed that TSG101 interacted with PEG10 and protected it from proteasomal degradation thereby regulating the expression of p53, p21 and MMPs. Finally, we found that both TSG101 and PEG10 proteins are up-regulated and presented a direct correlation in HCC patients. In conclusion, these results suggest that TSG101 is up-regulated in human HCC patients, which may accelerate the proliferation, migration and invasion of HCC cells through regulating PEG10.

Indexed as

Gene Expression Regulation, NeoplasticApoptosis Regulatory ProteinsCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportHep G2 CellsHumansLiver NeoplasmsMatrix MetalloproteinasesNeoplasm InvasivenessRNA-Binding ProteinsRNA InterferenceApoptosis Regulatory ProteinsCDKN1A protein, humanCyclin-Dependent Kinase Inhibitor p21DNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportMatrix MetalloproteinasesPEG10 protein, humanRNA-Binding ProteinsTIMP1 protein, humanTissue Inhibitor of Metalloproteinase-1Transcription FactorsTsg101 ProteinTumor Suppressor Protein p53HCCMMPsp21p53PEG10TSG101

Identifiers

PMID30450735
PMCPMC6307771
OpenAlexW2900544588

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.