Evidence map›Paper›PMID 35922412›Full record

ArticleCell death & disease2022

SOX15 transcriptionally increases the function of AOC1 to modulate ferroptosis and progression in prostate cancer.

Yinghui Ding, Yuankang Feng, Zhenlin Huang, Yu Zhang, Xiang Li, Ruoyang Liu, Hao Li, Tao Wang, Yafei Ding, Zhankui Jia and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 43 citations in OpenAlex.

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  16. [Functional study of amine oxidase copper-containing 1 (AOC1) in lipid metabolism].Sheng wu yi xue gong cheng xue za zhi = Journal of biomedical engineering = Shengwu yixue gongchengxue zazhi · 2024
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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

11 authors at 1 institution in 1 country.

Yinghui Ding *Department of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Yuankang Feng *Department of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Zhenlin Huang *Department of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Yu ZhangDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Xiang LiDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Ruoyang LiuDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Hao LiDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Tao WangDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Yafei DingDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China.
Zhankui JiaDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China. jiazhankui@126.com.
Jinjian YangDepartment of Urology, the First Affiliated Hospital of Zhengzhou University, 450052, Zhengzhou, China. hzlinok@126.com.ORCID 0000-0003-2089-4956
First Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amine oxidase copper-containing 1 (AOC1) is considered an oncogene in many types of tumors. Nevertheless, there have been no investigations of AOC1 and its regulatory mechanism in prostate cancer. Here, we reveal a novel action of AOC1 and a tumor suppressor mechanism in prostate cancer. AOC1 is downregulated in prostate cancer. Abatement of AOC1 in prostate cancer tissue is positively correlated with the tumor size, lymph node metastasis, and Gleason score for prostate cancer. Conversely, high expression of AOC1 is significantly associated with reduced proliferation and migration in prostate cancer both in vitro and in vivo. We show that the anticancer effect of AOC1 is mediated by its action on spermidine which leads to the activation of reactive oxygen species and ferroptosis. AOC1 expression in prostate cancer is positively regulated by the transcription factor SOX15. Therefore, SOX15 can transcriptionally promote AOC1 expression and strengthen this effect. Targeting AOC1 and SOX15 may be promising for the treatment of prostate cancer.

Indexed as

Amine Oxidase (Copper-Containing)FerroptosisProstatic NeoplasmsCell ProliferationGene Expression Regulation, NeoplasticHumansMaleSOX Transcription FactorsAmine Oxidase (Copper-Containing)SOX15 protein, humanSOX Transcription Factors

Identifiers

PMID35922412
PMCPMC9349193
OpenAlexW4289641871

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.