Evidence map›Paper›PMID 34002462›Full record

ArticleThe Kaohsiung journal of medical sciences2021

miRNA-10a-5p inhibits cell metastasis in hepatocellular carcinoma via targeting SKA1.

Duo Shen, Hong-Yu Zhao, Ai-Dong Gu, Yin-Wei Wu, Yu-Hang Weng, Shu-Jie Li, Jin-Yun Song, Xue-Feng Gu, Jie Qiu, Wei Zhao

Open access · goldAbstract read
In one paragraph

Article in The Kaohsiung journal of medical sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
1.3field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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 2 institutions in 1 country.

Duo ShenMedical School, Southeast University, Nanjing, China.ORCID https://orcid.org/0000-0002-2715-1090
Hong-Yu ZhaoDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0003-3244-9921
Ai-Dong GuDepartment of Hepatobiliary and Pancreatic Surgery, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-8955-2124
Yin-Wei WuDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-9465-2437
Yu-Hang WengDepartment of Hepatology, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0002-9988-6758
Shu-Jie LiDepartment of Hepatobiliary and Pancreatic Surgery, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0002-0396-568X
Jin-Yun SongDepartment of Clinical Research Center, The Second Hospital of Nanjing, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0002-3694-894X
Xue-Feng GuMedical School, Southeast University, Nanjing, China.ORCID https://orcid.org/0000-0002-7044-5502
Jie QiuMedical School, Southeast University, Nanjing, China.ORCID https://orcid.org/0000-0002-2238-9323
Wei ZhaoMedical School, Southeast University, Nanjing, China.ORCID https://orcid.org/0000-0001-5698-4844
Nanjing University of Chinese Medicine · CNSoutheast University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A variety of microRNAs (miRNAs) are involved in the occurrence and development of hepatocellular carcinoma (HCC). However, the role of miR-10a-5p in the progression of HCC remains unclear. Therefore, the purpose of this study was to determine the role of miR-10a-5p in the development of HCC and the possible molecular mechanism. miR-10a-5p expression in HCC tissues and plasma from patients was detected by quantitative real-time polymerase chain reaction. Migratory changes in HCC cells were detected after the overexpression of miR-10a-5p. Epithelial-mesenchymal transition (EMT)-related proteins were detected by Western blot. Finally, through luciferase assay and rescue experiments, the mechanism by which miR-10a-5p regulates its downstream gene, human spindle and kinetochore-associated complex subunit 1, SKA1 and the interaction between these molecules in the development of HCC were determined. The expression of miR-10a-5p was markedly downregulated in HCC tissues, cell lines, and plasma. The overexpression of miR-10a-5p significantly inhibited the migration, invasion, and EMT of HCC cells. Furthermore, SKA1 was shown to be a downstream gene of miR-10a-5p. SKA1 silencing had the same effect as miR-10a-5p overexpression in HCC. In particular, the overexpression of SKA1 reversed the inhibitory effects of miR-10a-5p in HCC. Taken together, low miR-10a-5p expression is associated with HCC progression. miR-10a-5p inhibits the malignant development of HCC by negatively regulating SKA1.

Indexed as

AdolescentCarcinoma, HepatocellularChromosomal Proteins, Non-HistoneDisease ProgressionEpithelial-Mesenchymal TransitionFemaleHumansLiver NeoplasmsMaleMicroRNAsNeoplasm MetastasisChromosomal Proteins, Non-HistoneMicroRNAsMIRN10 microRNA, humanSKA1 protein, humanepithelial-mesenchymal transitionhepatocellular carcinomamiR-10a-5pSKA1

Identifiers

PMID34002462
PMCPMC11896280
OpenAlexW3162481657

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.