Evidence map›Paper›PMID 38942821›Full record

ArticleScientific reports2024

Down-regulation of SLC14A1 in prostate cancer activates CDK1/CCNB1 and mTOR pathways and promotes tumor progression.

Jianbin Ma, Kaihua Xue, Yifan Jiang, Xinyang Wang, Dalin He, Peng Guo

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

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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.

Jianbin Ma *Department of Urology, Qujiang Hospital, Northwest Corner of Huang Qutou Road Number Two and Changming Road, Xi'an, 710061, Shaanxi, China.
Kaihua Xue *Department of Urology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yan-Ta West Road, Xi'an, 710061, Shaanxi, China.
Yifan JiangDepartment of Urology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yan-Ta West Road, Xi'an, 710061, Shaanxi, China.
Xinyang WangDepartment of Urology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yan-Ta West Road, Xi'an, 710061, Shaanxi, China.
Dalin HeDepartment of Urology, Qujiang Hospital, Northwest Corner of Huang Qutou Road Number Two and Changming Road, Xi'an, 710061, Shaanxi, China. hedl@mail.xjtu.edu.cn.
Peng GuoDepartment of Urology, The First Affiliated Hospital of Xi'an Jiaotong University, 277 Yan-Ta West Road, Xi'an, 710061, Shaanxi, China. guopeng661@mail.xjtu.edu.cn.

Funding

National Natural Science Foundation of China 82172797National Natural Science Foundation of China 82303836
6 · The paper itself

Abstract

Prostate cancer (PCa) is the most common cancer among men in the United States and the leading cause of cancer-related death. The Solute Carrier Family 14 Member 1 (SLC14A1) is a member of urea transporters which are important for the regulation of urine concentration. However, the physiological significance of SLC14A1 in PCa still remains unclear. In the present study, via bioinformatics analysis and experiments, we found that expression of SLC14A1 is significantly decreased in PCa progression, which could be attributed to hypermethylation on SLC14A1 promoter region. Moreover, its low expression and hypermethylation on SLC14A1 promoter are closely related to the poor prognosis of PCa patients. On the other hand, overexpression of SLC14A1 inhibited cell proliferation and metastasis while its overexpression also suppressed CDK1/CCNB1 pathway and mTOR/MMP-9 signaling pathway. Additionally, SLC14A1 expression is enriched in prostate basal-type cells. In summary, our study indicates that its low expression level and promoter hypermethylation of SLC14A1 may represent novel indicators for PCa progression and prognosis, and SLC14A1 could inhibit the progression of PCa.

Indexed as

CDC2 Protein KinaseDisease ProgressionDNA MethylationGene Expression Regulation, NeoplasticPromoter Regions, GeneticProstatic NeoplasmsSignal TransductionTOR Serine-Threonine KinasesCell Line, TumorCell MovementCell ProliferationDown-RegulationHumansMalePrognosisCDC2 Protein KinaseCDK1 protein, humanMTOR protein, humanTOR Serine-Threonine Kinases

Identifiers

PMID38942821
PMCPMC11213927

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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.