Evidence map›Paper›PMID 37436074›Full record

ArticleJournal of cellular and molecular medicine2023

PSMC4 promotes prostate carcinoma progression by regulating the CBX3-EGFR-PI3K-AKT-mTOR pathway.

Kaifeng Liu, Shengmin Zhang, Yongzhan Gong, Panyan Zhu, Weigan Shen, Qi Zhang

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

13 citing papers in PubMed, 31 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

6 authors at 3 institutions in 1 country.

Kaifeng LiuDepartment of Andrology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Shengmin ZhangDepartment of Andrology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Yongzhan GongDepartment of Andrology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Panyan ZhuDepartment of Andrology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Weigan ShenDepartment of Andrology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, China.
Qi ZhangDepartment of Urology, Zhejiang Provincial People's Hospital, Hangzhou, China.ORCID 0000-0003-3257-4351
Nanjing Drum Tower Hospital · CNNorthern Jiangsu People's Hospital · CNZhejiang Provincial People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteasome 26S subunit ATPase 4 (PSMC4) could regulate cancer progression. However, the function of PSMC4 in prostate carcinoma (PCa) progression requires further clarification. In the study, PSMC4 and chromobox 3 (CBX3) levels were verified by TCGA data and tissue microarrays. Cell counting kit-8, cell apoptosis, cell cycle, wound healing, transwell and xenograft tumour model assays were performed to verify biological functions of PSMC4 in PCa. RNA-seq, PCR, western blotting and co-IP assays were performed to verify the mechanism of PSMC4. Results showed that PSMC4 level was significantly increased in PCa tissues, and patients with PCa with a high PSMC4 level exhibited shorter overall survival. PSMC4 knockdown markedly inhibited cell proliferation, cell cycle and migration in vitro and in vivo, and significantly promoted cell apoptosis. Then further study revealed that CBX3 was a downstream target of PSMC4. PSMC4 knockdown markedly reduced CBX3 level, and inhibited PI3K-AKT-mTOR signalling. CBX3 overexpression markedly promoted epidermal growth factor receptor (EGFR) level. Finally, PSMC4 overexpression showed reverse effect in DU145 cells, and the effects of PSMC4 overexpression on cell proliferation, migration and clonal formation were rescued by the CBX3 knockdown, and regulated EGFR-PI3K-AKT-mTOR signalling. In conclusion, PSMC4 could regulate the PCa progression by mediating the CBX3-EGFR-PI3K-AKT-mTOR pathway. These findings provided a new target for PCa treatment.

Indexed as

CarcinomaProstatic NeoplasmsATPases Associated with Diverse Cellular ActivitiesCell Line, TumorCell MovementCell ProliferationChromosomal Proteins, Non-HistoneErbB ReceptorsHumansMalePhosphatidylinositol 3-KinasesProstateProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktTOR Serine-Threonine KinasesATPases Associated with Diverse Cellular ActivitiesCBX3 protein, humanChromosomal Proteins, Non-HistoneEGFR protein, humanErbB ReceptorsPhosphatidylinositol 3-KinasesProteasome Endopeptidase ComplexProto-Oncogene Proteins c-aktPSMC4 protein, humanTOR Serine-Threonine KinasesCBX3PI3K-AKT-mTOR pathwayprostate carcinomaPSMC4

Identifiers

PMID37436074
PMCPMC10424298
OpenAlexW4383999073

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.