Evidence map›Paper›PMID 40891362›Full record

ReviewJournal of enzyme inhibition and medicinal chemistry2025

The key enzyme PYCR1 in proline metabolism: a dual driver of cancer progression and fibrotic remodeling.

Peng Guo, Chenchun Wu, Tong Wang, Yajuan Song, Xiaozi Liu, Xiang Wang, Yuhan Zhu, Binyu Song, Yifu Zhu, Juan Zhang and 4 more

Abstract readReview
In one paragraph

Review in Journal of enzyme inhibition and medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  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
  7. 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

14 authors.

Peng GuoDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.ORCID 0009-0009-6873-5971
Chenchun WuThe First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, Henan Province, China.
Tong WangDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yajuan SongDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xiaozi LiuDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xiang WangDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yuhan ZhuDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Binyu SongDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yifu ZhuDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Juan ZhangDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Lei GuoDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Rui TaoDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Zhou YuDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Baoqiang SongDepartment of Plastic Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pyrroline-5-Carboxylate Reductase 1 (PYCR1), a member of the PYCR family, is a key enzyme in the proline biosynthesis pathway. Notably, PYCR1 was originally identified via genetic disease research, linking its mutations to the occurrence of cutis laxa. PYCR1 contributes to the pathogenesis of malignancies and fibrotic diseases via mechanisms involving metabolic reprogramming, Extracellular Matrix (ECM) remodelling, and redox homeostasis maintenance. PYCR1 upregulation has been reported in multiple malignancies including Hepatocellular Carcinoma (HCC), Lung Cancer (LC), Breast Cancer (BC), Bladder Cancer (BlC), and Gastric Cancer (GC), where it has been shown to promote cancer proliferation, migration, and therapy resistance, correlating significantly with advanced cancer stages and poor prognosis. On the other hand, in fibrotic disorders, PYCR1-mediated proline metabolism has been linked to the progression of pulmonary, myocardial, and cutaneous fibroses. Notably, although PYCR1-targeted small-molecule inhibitors have demonstrated therapeutic potential in preclinical studies, their clinical translation is yet to be validated.

Indexed as

Enzyme InhibitorsFibrosisNeoplasmsProlinePyrroline Carboxylate ReductasesAnimalsdelta-1-Pyrroline-5-Carboxylate ReductaseDisease ProgressionHumansMolecular Structuredelta-1-Pyrroline-5-Carboxylate ReductaseEnzyme InhibitorsProlinePyrroline Carboxylate Reductasescancerfibrosismetabolic reprogrammingproline metabolismPYCR1

Identifiers

PMID40891362
PMCPMC12406333

What OpenQuestion holds

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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 OpenQuestion graph.