Evidence map›Paper›PMID 39859489›Full record

ReviewInternational journal of molecular sciences2025

Cellular Signaling of Amino Acid Metabolism in Prostate Cancer.

Ping Yao, Shiqi Cao, Ziang Zhu, Yunru Wen, Yawen Guo, Wenken Liang, Jianling Xie

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. 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

7 authors.

Ping YaoSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.ORCID 0009-0006-0392-6046
Shiqi CaoSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.
Ziang ZhuSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.
Yunru WenSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.
Yawen GuoSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.
Wenken LiangSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.
Jianling XieSchool of Biology and Biological Engineering, South China University of Technology, University Town, Guangzhou 510006, China.ORCID 0000-0002-0588-8016

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer is one of the most common malignancies affecting men worldwide and a leading cause of cancer-related mortality, necessitating a deeper understanding of its underlying biochemical pathways. Similar to other cancer types, prostate cancer is also characterised by aberrantly activated metabolic pathways that support tumour development, such as amino acid metabolism, which is involved in modulating key physiological and pathological cellular processes during the progression of this disease. The metabolism of several amino acids, such as glutamine and methionine, crucial for tumorigenesis, is dysregulated and commonly discussed in prostate cancer. And the roles of some less studied amino acids, such as histidine and glycine, have also been covered in prostate cancer studies. Aberrant regulation of two major signalling pathways, mechanistic target of rapamycin (mTOR) and general amino acid control non-depressible 2 (GCN2), is a key driver of reshaping the amino acid metabolism landscape in prostate cancer. By summarising our current understanding of how amino acid metabolism is modulated in prostate cancer, here, we provide further insights into certain potential therapeutic targets for managing prostate cancer through metabolic interventions.

Indexed as

Amino AcidsProstatic NeoplasmsSignal TransductionAnimalsHumansMaleMetabolic Networks and PathwaysTOR Serine-Threonine KinasesAmino AcidsTOR Serine-Threonine Kinasesamino acidGCN2metabolic reprogrammingmTORprostate cancer

Identifiers

PMID39859489
PMCPMC11765784

What Socratic holds

Textmetadata
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 Socratic graph.