Evidence map›Paper›PMID 36950649›Full record

ArticleHeliyon2023

The somatic mutational landscape and role of the ARID1A gene in hepatocellular carcinoma.

Guang-Xiao Meng, Chun-Cheng Yang, Lun-Jie Yan, Ya-Fei Yang, Yu-Chuan Yan, Jian-Guo Hong, Zhi-Qiang Chen, Zhao-Ru Dong, Tao Li

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Circulating tumor DNA and its role in detection, prognosis and therapeutics of hepatocellular carcinoma.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2024
    Article
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.

Guang-Xiao MengDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Chun-Cheng YangDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Lun-Jie YanDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Ya-Fei YangDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Yu-Chuan YanDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Jian-Guo HongDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Zhi-Qiang ChenDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Zhao-Ru DongDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Tao LiDepartment of General Surgery, Qilu Hospital of Shandong University, Jinan, 250012, China.
Qilu Hospital of Shandong University · CNSecond Hospital of Shandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hepatocellular carcinoma (HCC) is one of the most common malignant tumours worldwide. Clarification of the somatic mutational landscape of important genes could reveal new therapeutic targets and facilitate individualized therapeutic approaches for HCC patients. The mutation and expression changes in the ARID1A gene in HCC remain controversial. Methods: First, cBioPortal was used to visualize genetic alterations and DNA copy number alterations (CNAs) in ARID1A. The relationships between ARID1A mutation status and HCC patient clinicopathological features and overall survival (OS) were also determined. Then, a meta-analysis was performed to evaluate the effect of ARID1A mutation or expression on the prognosis of HCC patients. Finally, the role of ARID1A in HCC progression was verified by Results: ARID1A mutation was detected in 9.35% (33/353) of sequenced HCC cases, and ARID1A mutation decreased ARID1A mRNA expression. Patients with ARID1A alterations presented worse OS than those without ARID1A alterations. Meta-analysis and human HCC tissue microarray (TMA) analysis revealed that HCC patients with low ARID1A expression had worse OS and relapse-free survival (RFS), and low ARID1A expression was negatively correlated with tumour size. Then, ARID1A gain-of-function and loss-of-function experiments demonstrated the tumour suppressor role of ARID1A in HCC Conclusions: ARID1A can be considered a potential prognostic biomarker and candidate therapeutic target for HCC.

Indexed as

ARID1AARID1A, AT-rich interaction domain 1ACCK-8, Cell Counting Kit-8EdU, 5-Ethyl-2'-deoxyuridineHCC, Hepatocellular carcinomaHepatocellular carcinomaOS, overall survivalPrognosisPrognostic biomarkerRBL1, regulating retinoblastoma-like 1RFS, relapse-free survival

Identifiers

PMID36950649
PMCPMC10025035
OpenAlexW4323349200

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.