Evidence map›Paper›PMID 35793868›Full record

ArticleJournal for immunotherapy of cancer2022

Inhibition of stearoyl-CoA desaturase 1 (SCD1) enhances the antitumor T cell response through regulating β-catenin signaling in cancer cells and ER stress in T cells and synergizes with anti-PD-1 antibody.

Yuki Katoh, Tomonori Yaguchi, Akiko Kubo, Takashi Iwata, Kenji Morii, Daiki Kato, Shigeki Ohta, Ryosuke Satomi, Yasuhiro Yamamoto, Yoshitaka Oyamada and 6 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
8.6field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 87 citations in OpenAlex.

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14 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

16 authors at 6 institutions in 1 country.

Yuki KatohDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0002-7467-3377
Tomonori YaguchiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan yutakawa@keio.jp yutakawa@iuhw.ac.jp yaguchi.tomonori.4m@kyoto-u.ac.jp.ORCID 0000-0002-2904-9030
Akiko KuboDepartment of Biochemistry, Keio University School of Medicine, Tokyo, Japan.
Takashi IwataDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Kenji MoriiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Daiki KatoDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Shigeki OhtaDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.
Ryosuke SatomiNational Hospital Organisation Tokyo Medical Center, Tokyo, Japan.
Yasuhiro YamamotoDepartment of Respiratory Medicine, The University of Tokyo, Tokyo, Japan.
Yoshitaka OyamadaNational Hospital Organisation Tokyo Medical Center, Tokyo, Japan.
Kota OuchiDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Shin TakahashiDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Chikashi IshiokaDepartment of Medical Oncology, Tohoku University Hospital, Sendai, Japan.
Ryo MatobaDNA Chip Research Inc, Tokyo, Japan.
Makoto SuematsuDepartment of Biochemistry, Keio University School of Medicine, Tokyo, Japan.
Yutaka KawakamiDivision of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan yutakawa@keio.jp yutakawa@iuhw.ac.jp yaguchi.tomonori.4m@kyoto-u.ac.jp.ORCID 0000-0002-0036-1186
Keio University · JPTohoku University · JPTokyo Medical Center · JPDNA Chip Research (Japan) · JPNihon University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUnderstanding the mechanisms of non-T cell inflamed tumor microenvironment (TME) and their modulation are important to improve cancer immunotherapies such as immune checkpoint inhibitors. The involvement of various immunometabolisms has recently been indicated in the formation of immunosuppressive TME. In this study, we investigated the immunological roles of stearoyl-CoA desaturase 1 (SCD1), which is essential for fatty acid metabolism, in the cancer immune response.

methodsWe investigated the roles of SCD1 by inhibition with the chemical inhibitor or genetic manipulation in antitumor T cell responses and the therapeutic effect of anti-programmed cell death protein 1 (anti-PD-1) antibody using various mouse tumor models, and their cellular and molecular mechanisms. The roles of SCD1 in human cancers were also investigated by gene expression analyses of colon cancer tissues and by evaluating the related free fatty acids in sera obtained from patients with non-small cell lung cancer who were treated with anti-PD-1 antibody.

resultsSystemic administration of a SCD1 inhibitor in mouse tumor models enhanced production of CCL4 by cancer cells through reduction of Wnt/β-catenin signaling and by CD8

conclusionsSCD1 expressed in cancer cells and immune cells causes immunoresistant conditions, and its inhibition augments antitumor T cells and therapeutic effects of anti-PD-1 antibody. Therefore, SCD1 is an attractive target for the development of new diagnostic and therapeutic strategies to improve current cancer immunotherapies including immune checkpoint inhibitors.

Indexed as

Carcinoma, Non-Small-Cell LungCD8-Positive T-LymphocytesColonic NeoplasmsLung NeoplasmsStearoyl-CoA DesaturaseAnimalsbeta CateninImmune Checkpoint InhibitorsMiceMice, KnockoutTumor MicroenvironmentWnt Signaling Pathwaybeta CateninCTNNB1 protein, mouseImmune Checkpoint InhibitorsScd1 protein, mouseStearoyl-CoA DesaturaseCD8-Positive T-LymphocytesDrug Therapy, CombinationImmunotherapyTumor Microenvironment

Identifiers

PMID35793868
PMCPMC9260842
OpenAlexW4284879432

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LicenceCC BY
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Registered trials

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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.