Evidence map›Paper›PMID 37845207›Full record

ArticleCell death & disease2023

Pyrroline-5-carboxylate reductase 1 reprograms proline metabolism to drive breast cancer stemness under psychological stress.

Bai Cui, Bin He, Yanping Huang, Cenxin Wang, Huandong Luo, Jinxin Lu, Keyu Su, Xiaoyu Zhang, Yuanyuan Luo, Zhuoran Zhao and 9 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

22 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  6. [Research Progress on the Role and Mechanisms of PYCR1 
in Tumorigenesis and Progression].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2026
    Review
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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

19 authors at 6 institutions in 3 countries.

Bai Cui *Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Bin He *Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yanping Huang *Department of Oncology, the First Affiliated Hospital of Dalian Medical University, Dalian, China.
Cenxin Wang *Institute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Huandong LuoInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Jinxin LuInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Keyu SuInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Xiaoyu ZhangInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yuanyuan LuoCAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian, China.
Zhuoran ZhaoInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yuqing YangInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Yunkun ZhangDepartment of Pathology, The Second Hospital of Dalian Medical University, Dalian, China.
Fan AnInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China.
Hong WangDepartment of Orthopaedics, The Central Hospital of Dalian University of Technology, Dalian, China.
Eric W-F LamDepartment of Surgery and Cancer, Imperial College London, London, UK.ORCID 0000-0003-1274-3576
Keith W KelleyDepartment of Pathology, College of Medicine and Department of Animal Sciences, College of ACES, University of Illinois at Urbana-Champaign, Urbana, Illinois, USA.
Ling WangDepartment of Oncology, the First Affiliated Hospital of Dalian Medical University, Dalian, China. wangling@firsthosp-dmu.com.
Quentin LiuInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China. liuq9@mail.sysu.edu.cn.ORCID 0000-0002-0999-9805
Fei PengInstitute of Cancer Stem Cell, Dalian Medical University, Dalian, China. pengfei@dmu.edu.cn.ORCID 0000-0003-0772-0273
Dalian Medical University · CNSun Yat-sen University · CNDalian Institute of Chemical Physics · CNDalian University of Technology · CNImperial College London · GBUniversity of Illinois Urbana-Champaign · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem-like cells (CSCs) contribute to cancer metastasis, drug resistance and tumor relapse, yet how amino acid metabolism promotes CSC maintenance remains exclusive. Here, we identify that proline synthetase PYCR1 is critical for breast cancer stemness and tumor growth. Mechanistically, PYCR1-synthesized proline activates cGMP-PKG signaling to enhance cancer stem-like traits. Importantly, cGMP-PKG signaling mediates psychological stress-induced cancer stem-like phenotypes and tumorigenesis. Ablation of PYCR1 markedly reverses psychological stress-induced proline synthesis, cGMP-PKG signaling activation and cancer progression. Clinically, PYCR1 and cGMP-PKG signaling components are highly expressed in breast tumor specimens, conferring poor survival in breast cancer patients. Targeting proline metabolism or cGMP-PKG signaling pathway provides a potential therapeutic strategy for breast patients undergoing psychological stress. Collectively, our findings unveil that PYCR1-enhanced proline synthesis displays a critical role in maintaining breast cancer stemness.

Indexed as

Breast Neoplasmsdelta-1-Pyrroline-5-Carboxylate ReductaseFemaleHumansNeoplasm Recurrence, LocalOxidoreductasesProlinePyrrolesdelta-1-pyrroline-5-carboxylatedelta-1-Pyrroline-5-Carboxylate ReductaseOxidoreductasesProlinePyrroles

Identifiers

PMID37845207
PMCPMC10579265
OpenAlexW4387668031

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.