Evidence map›Paper›PMID 34401050›Full record

ArticleJournal of extracellular vesicles2021

TPI1-reduced extracellular vesicles mediated by Rab20 downregulation promotes aerobic glycolysis to drive hepatocarcinogenesis.

Bonnie Hei Man Liu, Sze Keong Tey, Xiaowen Mao, Angel Po Yee Ma, Cherlie Lot Sum Yeung, Samuel Wan Ki Wong, Tung Him Ng, Yi Xu, Yue Yao, Eva Yi Man Fung and 8 more

Open access · goldAbstract read
In one paragraph

Article in Journal of extracellular vesicles, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.7field-weighted citation impact, top 5% 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

33 citing papers in PubMed, 58 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

18 authors at 6 institutions in 2 countries.

Bonnie Hei Man LiuDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Sze Keong TeyDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Xiaowen MaoDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Angel Po Yee MaDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Cherlie Lot Sum YeungDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Samuel Wan Ki WongDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Tung Him NgDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Yi XuDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Yue YaoDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Eva Yi Man FungDepartment of Chemistry State Key Laboratory of Synthetic Chemistry The University of Hong Kong Hong Kong China.
Kel Vin TanDepartment of Diagnostic Radiology Queen Mary Hospital the University of Hong Kong Hong Kong China.
Pek-Lan KhongDepartment of Diagnostic Radiology Queen Mary Hospital the University of Hong Kong Hong Kong China.
Daniel Wai-Hung HoDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Irene Oi-Lin NgDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Alexander Hin Ning TangDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.
Shao Hang CaiDepartment of Infectious Diseases Nanfang Hospital Southern Medical University Guangzhou China.
Jing Ping YunDepartment of Pathology Sun Yat-sen University Cancer Centre Guangzhou China.
Judy Wai Ping YamDepartment of Pathology Li Ka Shing Faculty of Medicine The University of Hong Kong Hong Kong China.ORCID 0000-0002-5637-121X
University of Hong Kong · HKHarbin Medical University · CNQueen Mary Hospital · CNNanfang Hospital · CNState Key Laboratory of Synthetic Chemistry · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rab GTPases are major mediators that ensure the proper spatiotemporal regulation of intracellular trafficking. Functional impairment and altered expression of Rab proteins have been revealed in various human cancers. There is an emerging evidence about the role of Rab proteins in the biogenesis of extracellular vesicles (EVs). In hepatocellular carcinoma (HCC), using RNA sequencing comparing expression profiles of adjacent non-tumorous tissues and HCC, Rab20 is identified to be the most frequently downregulated Rab member in HCC. Functionally, restoration of Rab20 in metastatic HCC cells results in the release of EVs with a diminished activity to promote cell growth, motility and metastasis. Conversely, EVs released from normal liver cells with Rab20 knockdown loses suppressive effect on HCC cell growth and motility. Proteomic profiling revealed the level of triosephosphate isomerase 1 (TPI1), a glycolytic enzyme, in EVs to be positively associated with Rab20 expression of the releasing cells. TPI1 targeted to be expressed in EVs released by Rab20 knockdown cells compromises the oncogenic activity of EVs. Besides, EVs released by TPI1 knockdown cells recapitulates the promoting effect of EVs derived from HCC cells with Rab20 underexpression. Aerobic glycolysis is beneficial to the survival and proliferation of tumour cells. Here, we observed that the enhanced cell growth and motility are driven by the enhanced aerobic glycolysis induced by EVs with reduced TPI1. The addition of glycolytic inhibitor blocks the promoting effect of EVs with reduced TPI1. Taken together, our study provides a mechanistic link among tumour cell-derived EVs and glucose metabolism in HCC with Rab20 deregulation.

Indexed as

GlycolysisCarcinogenesisCarcinoma, HepatocellularCell Line, TumorCell MovementExtracellular VesiclesGene Expression ProfilingGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansLiver Neoplasmsrab GTP-Binding ProteinsSequence Analysis, RNATriose-Phosphate IsomeraseRab20 protein, humanrab GTP-Binding ProteinsTriose-Phosphate Isomeraseextracellular vesiclesglycolysishepatocellular carcinomaRab20 GTPasetriosephosphate isomerase 1

Identifiers

PMID34401050
PMCPMC8357635
OpenAlexW3190817209

What OpenQuestion holds

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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.