Evidence map›Paper›PMID 38918720›Full record

ArticleClinical proteomics2024

Proteomic profiling of prostate cancer reveals molecular signatures under antiandrogen treatment.

Yurun Huang, Guanglin Yang, Xinpeng Yao, Yue Fang, Qiliang Lin, Menghan Zhou, Yiping Yang, Qinggui Meng, Qingyun Zhang, Shan Wang

Abstract read
In one paragraph

Article in Clinical proteomics, 2024. 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
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Cellular Signaling of Amino Acid Metabolism in Prostate Cancer.International journal of molecular sciences · 2025
    Review
  4. 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

10 authors.

Yurun Huang *Department of Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Guanglin Yang *Department of Urology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Xinpeng Yao *The First Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Yue FangThe First Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Qiliang LinThe First Clinical Medical College, Guangxi Medical University, Nanning, Guangxi, China.
Menghan ZhouDepartment of Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Yiping YangDepartment of Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Qinggui MengDepartment of Urology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China.
Qingyun ZhangDepartment of Urology, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China. zqy628@163.com.
Shan WangDepartment of Research, Guangxi Medical University Cancer Hospital, Nanning, Guangxi, China. wangshan@sr.gxmu.edu.cn.

Funding

Natural Science Foundation of Guangxi 2020GXNSFAA297265
6 · The paper itself

Abstract

backgroundTumorigenesis and progression of prostate cancer (PCa) are indispensably dependent on androgen receptor (AR). Antiandrogen treatment is the principal preference for patients with advanced PCa. However, the molecular characteristics of PCa with antiandrogen intervention have not yet been fully uncovered.

methodsWe first performed proteome analysis with 32 PCa tumor samples and 10 adjacent tissues using data-independent acquisition (DIA)- parallel accumulation serial fragmentation (PASEF) proteomics. Then label-free quantification (LFQ) mass spectrometry was employed to analyze protein profiles in LNCaP and PC3 cells.

resultsM-type creatine kinase CKM and cartilage oligomeric matrix protein COMP were demonstrated to have the potential to be diagnostic biomarkers for PCa at both mRNA and protein levels. Several E3 ubiquitin ligases and deubiquitinating enzymes (DUBs) were significantly altered in PCa and PCa cells under enzalutamide treatment, and these proteins might reprogram proteostasis at protein levels in PCa. Finally, we discovered 127 significantly varied proteins in PCa samples with antiandrogen therapy and further uncovered 4 proteins in LNCaP cells upon enzalutamide treatment.

conclusionsOur research reveals new potential diagnostic biomarkers for prostate cancer and might help resensitize resistance to antiandrogen therapy.

Indexed as

AntiandrogenDeubiquitinaseDiagnostic biomarkersE3 ubiquitin ligaseProstate CancerProteomics

Identifiers

PMID38918720
PMCPMC11202386

What Socratic holds

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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 Socratic graph.