Evidence map›Paper›PMID 30158600›Full record

ReviewCell death & disease2018

Prolyl isomerase Pin1: a promoter of cancer and a target for therapy.

Yang Chen, Ya-Ran Wu, Hong-Ying Yang, Xin-Zhe Li, Meng-Meng Jie, Chang-Jiang Hu, Yu-Yun Wu, Shi-Ming Yang, Ying-Bin Yang

Open access · goldAbstract readReview
In one paragraph

Review in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 103 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 2 pooled it
6.0field-weighted citation impact, top 3% 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

103 citing papers in PubMed, 2 syntheses or guidelines pooled it, 154 citations in OpenAlex.

  1. Pooled it
  2. Prognostic value of peptidyl-prolyl cis-trans isomerase 1 (PIN1) in human malignant tumors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2020
    Pooled it
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  15. Programmable immunoprobiotics orchestrate antitumor immune response with Pin1 inhibition for pancreatic cancer treatment.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
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  19. Review
  20. Beneficial Effects of PIN1 Inhibition on Diabetes Mellitus: A Concise Review.Endocrine, metabolic & immune disorders drug targets · 2025
    Review

43 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Yang ChenSchool of Life Science, Southwest University. No.1, Tiansheng Road, Beibei District, 400715, Chongqing, China.
Ya-Ran WuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University. No.183, Xinqiao Main Street, Shapingba District, 400037, Chongqing, China.
Hong-Ying YangSchool of Life Science, Southwest University. No.1, Tiansheng Road, Beibei District, 400715, Chongqing, China.
Xin-Zhe LiDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University. No.183, Xinqiao Main Street, Shapingba District, 400037, Chongqing, China.
Meng-Meng JieDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University. No.183, Xinqiao Main Street, Shapingba District, 400037, Chongqing, China.
Chang-Jiang HuDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University. No.183, Xinqiao Main Street, Shapingba District, 400037, Chongqing, China.
Yu-Yun WuSchool of Life Science, Southwest University. No.1, Tiansheng Road, Beibei District, 400715, Chongqing, China.
Shi-Ming YangDepartment of Gastroenterology, Xinqiao Hospital, Third Military Medical University. No.183, Xinqiao Main Street, Shapingba District, 400037, Chongqing, China. shimingyang@yahoo.com.
Ying-Bin YangSchool of Life Science, Southwest University. No.1, Tiansheng Road, Beibei District, 400715, Chongqing, China. yybin@swu.edu.cn.
Southwest University · CNArmy Medical University · CNXinqiao Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pin1 is the only known peptidyl-prolyl cis-trans isomerase (PPIase) that specifically recognizes and isomerizes the phosphorylated Serine/Threonine-Proline (pSer/Thr-Pro) motif. The Pin1-mediated structural transformation posttranslationally regulates the biofunctions of multiple proteins. Pin1 is involved in many cellular processes, the aberrance of which lead to both degenerative and neoplastic diseases. Pin1 is highly expressed in the majority of cancers and its deficiency significantly suppresses cancer progression. According to the ground-breaking summaries by Hanahan D and Weinberg RA, the hallmarks of cancer comprise ten biological capabilities. Multiple researches illuminated that Pin1 contributes to these aberrant behaviors of cancer via promoting various cancer-driving pathways. This review summarized the detailed mechanisms of Pin1 in different cancer capabilities and certain Pin1-targeted small-molecule compounds that exhibit anticancer activities, expecting to facilitate anticancer therapies by targeting Pin1.

Indexed as

AnimalsAntineoplastic AgentsHumansNeoplasmsPeptidylprolyl IsomerasePromoter Regions, GeneticSignal TransductionSmall Molecule LibrariesAntineoplastic AgentsPeptidylprolyl IsomeraseSmall Molecule Libraries

Identifiers

PMID30158600
PMCPMC6115400
OpenAlexW2889021210

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.