Evidence map›Paper›PMID 37520264›Full record

ArticlePeerJ2023

DNAJ heat shock protein family member C1 can regulate proliferation and migration in hepatocellular carcinoma.

Yu-Chun Fan, Zhi-Yong Meng, Chao-Sheng Zhang, De-Wei Wei, Wan-Shuo Wei, Xian-Dong Xie, Ming-Lu Huang, Li-He Jiang

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 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

8 authors at 4 institutions in 1 country.

Yu-Chun FanMedical College, Guangxi University, Nanning, Guangxi, China.
Zhi-Yong MengFirst Clinical Medical College, Guangxi Traditional Chinese Medical University, Nanning, China.
Chao-Sheng ZhangSchool of Basic Medical Sciences, Youjiang Medical University for Nationalities, Baise, China.
De-Wei WeiSchool of Stomatology, Youjiang Medical University for Nationalities, Baise, China.
Wan-Shuo WeiSchool of Basic Medical Sciences, Youjiang Medical University for Nationalities, Baise, China.
Xian-Dong XieSchool of Basic Medical Sciences, Youjiang Medical University for Nationalities, Baise, China.
Ming-Lu HuangSchool of Stomatology, Youjiang Medical University for Nationalities, Baise, China.
Li-He JiangMedical College, Guangxi University, Nanning, Guangxi, China.
Affiliated Hospital of Youjiang Medical University for Nationalities · CNBlood Center of Zhejiang Province · CNGuangxi University · CNGuangxi University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: DNAJ heat shock protein family (Hsp40) member C1(DNAJC1) is a member of the DNAJ family. Some members of the DNAJ gene family had oncogenic properties in many cancers. However, the role of DNAJC1 in hepatocellular carcinoma (HCC) was unclear. Methods: In this study, expression and prognostic value of DNAJC1 in HCC were analyzed by bioinformatics. Quantitative real-time PCR and Western blotting were used to verify DNAJC1 expression in liver cancer cell lines. Furthermore, immunohistochemical (IHC) was used to detect DNAJC1 expression in liver cancer tissues. Subsequently, the effect of DNAJC1 on the proliferation, migration, invasion and apoptosis of HCC cells was detected by knocking down DNAJC1. Finally, gene set enrichment analysis (GSEA) was used to investigate the potential mechanism of DNAJC1 and was verified by Western blotting. Results: DNAJC1 was highly expressed in HCC and was significantly associated with the prognosis of patients with HCC. Importantly, the proliferation, migration and invasion of Huh7 and MHCC97H cells were inhibited by the knockdown of DNAJC1 and the knockdown of DNAJC1 promoted Huh7 and MHCC97H cell apoptosis. Furthermore, compared to the negative control group, DNAJC1 knockdown in Huh7 and MHCC97H cells promoted the expression of p21, p53, p-p53(Ser20), Bax and E-cadherin proteins, while inhibiting the expression of PARP, MMP9, Vimentin, Snai1, Bcl-2 and N-cadherin proteins. Conclusions: DNAJC1 had a predictive value for the prognosis of HCC. Knockdown of DNAJC1 may inhibit HCC cell proliferation, migration and invasion and promote the HCC cell apoptosis through p53 and EMT signaling pathways.

Indexed as

Carcinoma, HepatocellularCell MovementCell ProliferationHSP40 Heat-Shock ProteinsLiver NeoplasmsApoptosisCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisHSP40 Heat-Shock ProteinsBioinformatic analysisDNAJC1Hepatocellular carcinoma

Identifiers

PMID37520264
PMCPMC10386825
OpenAlexW4385281311

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LicenceCC BY
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Registered trials

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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.