Evidence map›Paper›PMID 37452654›Full record

ArticleMolecular oncology2023

ANGPTL2-mediated epigenetic repression of MHC-I in tumor cells accelerates tumor immune evasion.

Tsuyoshi Kadomatsu, Chiaki Hara, Ryoma Kurahashi, Haruki Horiguchi, Jun Morinaga, Keishi Miyata, Sohtaro Kurano, Hisashi Kanemaru, Satoshi Fukushima, Kimi Araki and 4 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2023. 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
1.8field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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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

14 authors at 2 institutions in 2 countries.

Tsuyoshi KadomatsuDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.ORCID 0000-0003-3327-6954
Chiaki HaraDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.
Ryoma KurahashiDepartment of Urology, Graduate School of Medical Sciences, Kumamoto University, Japan.
Haruki HoriguchiDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.
Jun MorinagaDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.
Keishi MiyataDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.
Sohtaro KuranoDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.
Hisashi KanemaruDepartment of Dermatology and Plastic Surgery, Graduate School of Medical Sciences, Kumamoto University, Japan.
Satoshi FukushimaDepartment of Dermatology and Plastic Surgery, Graduate School of Medical Sciences, Kumamoto University, Japan.
Kimi ArakiCenter for Metabolic Regulation of Healthy Aging (CMHA), Graduate School of Medical Sciences, Kumamoto University, Japan.
Masaya BabaInternational Research Center for Medical Sciences (IRCMS), Kumamoto University, Japan.
W Marston LinehanUrologic Oncology Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD, USA.
Tomomi KambaDepartment of Urology, Graduate School of Medical Sciences, Kumamoto University, Japan.
Yuichi OikeDepartment of Molecular Genetics, Graduate School of Medical Sciences, Kumamoto University, Japan.ORCID 0000-0003-3245-5395
Kumamoto University · JPNational Cancer Institute · US

Funding

Ichiro Kanehara Foundation for the Promotion of Medical Sciences and Medical CareKato Memorial Bioscience FoundationMinistry of Education, Culture, Sports, Science and Technology 21K07101Ministry of Education, Culture, Sports, Science and Technology 21K15508
6 · The paper itself

Abstract

Loss or downregulation of major histocompatibility complex class I (MHC-I) contributes to tumor immune evasion. We previously demonstrated that angiopoietin-like protein 2 (ANGPTL2) promotes tumor progression using a Xp11.2 translocation renal cell carcinoma (tRCC) mouse model. However, molecular mechanisms underlying ANGPTL2 tumor-promoting activity in the tRCC model remained unclear. Here, we report that ANGPTL2 deficiency in renal tubular epithelial cells slows tumor progression in the tRCC mouse model and promotes activated CD8

Indexed as

Carcinoma, Renal CellKidney NeoplasmsAngiopoietin-Like Protein 2Angiopoietin-like ProteinsAnimalsDisease Models, AnimalEpigenetic RepressionHistocompatibility Antigens Class IMiceTumor EscapeAngiopoietin-Like Protein 2Angiopoietin-like ProteinsHistocompatibility Antigens Class IANGPTL2H3K27me3MHC-IPRC2tumor immune evasion

Identifiers

PMID37452654
PMCPMC10701769
OpenAlexW4384401262

What OpenQuestion 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 OpenQuestion graph.