Evidence map›Paper›PMID 34664737›Full record

ArticleJournal of clinical laboratory analysis2021

Hsa_circ_0001806 promotes glycolysis and cell progression in hepatocellular carcinoma through miR-125b/HK2.

Xueyi Chen, Pengyun She, Caihua Wang, Lina Shi, Tieying Zhang, Yanfei Wang, Haixia Li, Lu Qian, Man Li

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

7 citing papers in PubMed, 15 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 2 institutions in 1 country.

Xueyi ChenCollege of Life Sciences, Northwest University, Xi'an, China.
Pengyun SheThe First Affliliated Hospital of Xi'an Jiao Tong University, Xi'an, China.
Caihua WangCollege of Life Sciences, Northwest University, Xi'an, China.
Lina ShiDepartment of Endocrinology, The Affiliated Hospital of Northwest University Xi'an NO.3 Hospital, Xi'an, China.
Tieying ZhangDepartment of Neurology, The Affiliated Hospital of Northwest University Xi'an NO.3 Hospital, Xi'an, China.
Yanfei WangDepartment of Neurology, The Affiliated Hospital of Northwest University Xi'an NO.3 Hospital, Xi'an, China.
Haixia LiDepartment of Geriatrics, Xianyang first people's Hospital, Xianyang, China.
Lu QianXi'an Key Laboratory of Cardiovascular and Cerebrovascular Diseases, The Affiliated Hospital of Northwest University Xi'an NO.3 Hospital, Xi'an, China.ORCID https://orcid.org/0000-0003-2382-0688
Man LiDepartment of Internal Medicine, The Affiliated Hospital of Northwest University Xi'an NO.3 Hospital, Xi'an, China.
Northwest University · CNXian Yang Central Hospital · CN

Funding

Science and Technology Planning Project of Xi'an of China 2019114613YX001SF035
6 · The paper itself

Abstract

objectiveHepatocellular carcinoma (HCC) is one of the most common malignant tumours and a leading cause of cancer death. Circular RNA (circRNA) has been demonstrated to play an important role in regulating tumour development. The current study aims to explore the specific role of hsa_circ_0001806 during HCC progression.

methodsThe expression of hsa_circ_0001806 in HCC tissues and cells was measured through qRT-PCR. Cell proliferation, apoptosis and migration were measured using CCK-8 and Annexin V/PI staining kits, and Transwell assay. Bioinformatics prediction and dual-luciferase reporter assay were adopted to explore the mechanism underlying the cell function of hsa_circ_0001806 in HCC cells. In addition, glycolysis was assessed by measuring the glucose uptake, lactate production and ATP level using a glucose assay kit, fluorometric lactate assay kit and ATP detection assay kit.

resultsHsa_circ_0001806 was up-regulated in HCC tissues and cells and positively associated with the advanced TNM stage, metastasis and poor overall survival. The overexpression of hsa_circ_0001806 promoted HCC cell proliferation, migration and glycolysis and inhibited cell apoptosis, while the silence of hsa_circ_0001806 showed an opposite effect. Furthermore, hsa_circ_0001806 acted as a sponge of miR-125b to up-regulate hexokinase II (HK2) expression. In addition, the inhibition of miR-125b and HK2 overexpression partly reversed the inhibitory effect of hsa_circ_0001806 silencing on HCC cell proliferation, migration and glycolysis.

conclusionThe inhibition of hsa_circ_0001806 suppressed HCC cell proliferation, migration and glycolysis through mediating miR-125b/HK2 axis.

Indexed as

AdultApoptosisCarcinoma, HepatocellularCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticGlycolysisHexokinaseHumansLiver NeoplasmsMaleMicroRNAsMiddle AgedPrognosisRNA, CircularHexokinaseHK2 protein, humanMicroRNAsMIRN125 microRNA, humanRNA, Circularglycolysishepatocellular carcinomaHK2hsa_circ_0001806miR-125b

Identifiers

PMID34664737
PMCPMC8649327
OpenAlexW3207328127

What OpenQuestion holds

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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.