Evidence map›Paper›PMID 37351671›Full record

ArticleDiscover oncology2023

HSF1 is a novel prognostic biomarker in high-risk prostate cancer that correlates with ferroptosis.

GaoZhen Jia, WenBo Wu, Lei Chen, Yang Yu, QiLin Tang, HaiTao Liu, Qi Jiang, BangMin Han

Open access · goldAbstract read
In one paragraph

Article in Discover oncology, 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
3.9field-weighted citation impact, top 6% 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, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Important molecular mechanisms in ferroptosis.Molecular and cellular biochemistry · 2025
    Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Mechanisms and regulations of ferroptosis.Frontiers in immunology · 2023
    Review
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 2 institutions in 1 country.

GaoZhen Jia *Department of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
WenBo Wu *Department of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
Lei Chen *Department of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
Yang YuDepartment of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
QiLin TangDepartment of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
HaiTao LiuDepartment of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China.
Qi JiangDepartment of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China. jqjq2007@126.com.
BangMin HanDepartment of Urology, Shanghai General Hospital (Shanghai Peoples Hospital 1), Shanghai JiaoTong University School of Medicine, Shanghai, 200080, China. hanbm@163.com.
Shanghai Jiao Tong University · CNShanghai First People's Hospital · CN

Funding

National Natural Science Foundation of China 81972371National Natural Science Foundation of China 81972407
6 · The paper itself

Abstract

backgroundProstate cancer (PC) is the most common cancer in older men in Europe and the United States and has the second highest death rate among male cancers. The transcription of heat shock proteins by Heat shock factor 1 (HSF1) is known to regulate cell growth and stress. Nevertheless, the impact of HSF1 on ferroptosis in PC through heat shock protein 10 (HSPE1) remains unexplored.

methodsThis study employed a range of analytical techniques, including proteomics sequencing, LC-MS/MS, CHIP-qPCR, Western blotting, immunohisto -chemistry, JC-1, CKK-8, MDA, and ROS assays. Bioinformatics analysis was performed using the UALCAN,GEPIA, PCaDB and Metascape platforms.

resultsCompared with levels observed in tumor-adjacent tissue, the levels of proteins associated with fatty acids, amino acids and the oxidative phosphorylation metabolic pathway were significantly upregulated in high-risk PC tissue (Gleason score ≥ 8). HSF1 mRNA and protein levels in high-risk PC tissues were significantly higher than those observed in medium-risk PC (Gleason score = 7) and low-risk PC (Gleason score ≤ 6) tissues. ssGSEA showed that HSF1 was involved in the proliferation and anti-apoptotic processes of PC. Further bioinformatics analysis showed that HSF1 potentially affects the mitochondrial oxidative phosphorylation (OXPHOS) system by targeting HSPE1. In addition, HSF1 alleviates ROS and MDA levels to enhance the resistance of prostate cancer cells to ferroptosis by regulating HSPE1 in vitro, and HSF1 knockout promotes the susceptibility of PC to RSL3 treatment by increasing ferroptosis in vivo.

conclusionCollectively, our findings suggest that HSF1 exerts a significant influence on PC. HSF1 may represent a promising biomarker for identifying high-risk PC, and the elimination of HSF1 could potentially enhance the therapeutic effectiveness of RSL3.

Indexed as

FerroptosisHigh-risk prostate cancerHSF1HSPE1RSL3

Identifiers

PMID37351671
PMCPMC10290025
OpenAlexW4381715731

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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.