Evidence map›Paper›PMID 35475476›Full record

ArticleClinical science (London, England : 1979)2022

ANGPTL1 attenuates cancer migration, invasion, and stemness through regulating FOXO3a-mediated SOX2 expression in colorectal cancer.

Ting-Yu Chang, Kuo-Cheng Lan, Chen-Yuan Chiu, Meei-Ling Sheu, Shing-Hwa Liu

Open access · greenAbstract read
In one paragraph

Article in Clinical science (London, England : 1979), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

16 citing papers in PubMed, 13 citations in OpenAlex.

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  11. Non-alcoholic fatty liver disease and liver secretome.Archives of pharmacal research · 2022
    Review
  12. Article
  13. ANGPTL1, Foxo3a-Sox2, and colorectal cancer metastasis.Clinical science (London, England : 1979) · 2022
    Article
  14. Article
  15. Article
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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

5 authors at 5 institutions in 1 country.

Ting-Yu ChangGraduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Kuo-Cheng LanDepartment of Emergency Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Chen-Yuan ChiuCenter of Consultation, Center for Drug Evaluation, Taipei, Taiwan.
Meei-Ling SheuInstitute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan.
Shing-Hwa LiuGraduate Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan.ORCID 0000-0002-9976-1197
Development Center for Biotechnology · TWNational Defense Medical Center · TWNational Taipei University · TWNational Taiwan University · TWNational Taiwan University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiopoietin-like protein 1 (ANGPTL1) is a member of the ANGPTL family that suppresses angiogenesis, cancer invasion, metastasis, and cancer progression. ANGPTL1 is down-regulated in various cancers including colorectal cancer (CRC); however, the effects and mechanisms of ANGPTL1 on liver metastasis and cancer stemness in CRC are poorly understood. In the present study, we identified that ANGPTL1 was down-regulated in CRC and inversely correlated with metastasis and poor clinical outcomes in CRC patients form the ONCOMINE database and Human Tissue Microarray staining. ANGPTL1 significantly suppressed the migration/invasion abilities, the expression of cancer stem cell (CSC) markers, and sphere formation by enhancing FOXO3a expression, which contributed to the reduction of stem cell transcription factor SOX2 expression in CRC cells. Consistently, overexpression of ANGPTL1 reduced liver metastasis, tumor growth, and tumorigenicity in tumor-bearing mice. ANGPTL1 expression was negatively correlated with CSC markers expression and poor clinical outcomes in CRC patients. Taken together, these findings demonstrate that the molecular mechanisms of ANGPTL1 in colorectal cancer stem cell progression may provide a novel therapeutic strategy for CRC.

Indexed as

Colorectal NeoplasmsLiver NeoplasmsAngiopoietin-Like Protein 1Angiopoietin-like ProteinsAnimalsCell Line, TumorCell ProliferationForkhead Box Protein O3Gene Expression Regulation, NeoplasticHumansMiceNeoplastic Stem CellsSOXB1 Transcription FactorsAngiopoietin-Like Protein 1Angiopoietin-like ProteinsANGPTL1 protein, humanForkhead Box Protein O3FOXO3 protein, humanSOX2 protein, humanSOXB1 Transcription FactorsANGPTL1cancer stem cellcolorectal cancerFOXO3aliver metastasisSOX2

Identifiers

PMID35475476
PMCPMC9093149
OpenAlexW4225003155

What OpenQuestion holds

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LicenceCC BY-NC-ND
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 OpenQuestion graph.