Evidence map›Paper›PMID 41132962›Full record

ArticleTranslational lung cancer research2025

The difference in tumor immune microenvironment and IFN-γ response between solid and non-solid adenocarcinoma.

Shuichi Shinohara, Daisuke Muraoka, Ayako Demachi-Okamura, Katsuhiro Masago, Eiichi Sasaki, Reina Nishida, Shin Shomura, Takashi Ohki, Yoshiki Shigematsu, Fumiaki Watanabe and 9 more

Abstract read
In one paragraph

Article in Translational lung cancer research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

19 authors.

Shuichi ShinoharaDivision of Translational Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Daisuke MuraokaDivision of Translational Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Ayako Demachi-OkamuraDivision of Translational Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Katsuhiro MasagoDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center Hospital, Nagoya, Japan.
Eiichi SasakiDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center Hospital, Nagoya, Japan.
Reina NishidaDivision of Translational Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Shin ShomuraDepartment of Thoracic Surgery, Mie Prefectural General Medical Center, Yokkaichi, Japan.
Takashi OhkiDepartment of Respiratory Surgery, Ichinomiya Nishi Hospital, Ichinomiya, Japan.
Yoshiki ShigematsuDepartment of Respiratory Surgery, Ichinomiya Nishi Hospital, Ichinomiya, Japan.
Fumiaki WatanabeDepartment of Thoracic Surgery, Mie-chuo Medical Center, Tsu, Japan.
Katsutoshi AdachiDepartment of Thoracic Surgery, Mie-chuo Medical Center, Tsu, Japan.
Kazuya FujinagaDepartment of Thoracic Surgery, Anjo Kosei Hospital, Anjo, Japan.
Shinji KanedaDepartment of Thoracic and Cardiovascular Surgery, Mie University Graduate School of Medicine, Tsu, Japan.
Motoshi TakaoDepartment of Thoracic and Cardiovascular Surgery, Mie University Graduate School of Medicine, Tsu, Japan.
Hiroaki KurodaDepartment of Respiratory Surgery, Teikyo University, Kanagawa, Japan.
Takashi OhtsukaDivision of Thoracic Surgery, Department of Surgery, The Jikei University School of Medicine, Tokyo, Japan.
Rui YamaguchiDivision of Cancer System Biology, Aichi Cancer Center Research Institute, Nagoya, Japan.
Tsukasa NabekuraDivision of Immune Response, Aichi Cancer Center Research Institute, Nagoya, Japan.
Hirokazu MatsushitaDivision of Translational Oncoimmunology, Aichi Cancer Center Research Institute, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Solid subtype adenocarcinomas have poor prognosis. Interferon-γ (IFN-γ) is a critical cytokine related to anti-tumor response in the tumor immune microenvironment. We aimed to identify the prognostic factors related to IFN-γ responsiveness. Methods: A total of 112 lung adenocarcinoma samples were obtained from patients who underwent surgery between 2014 and 2020. DNA and RNA were extracted and analyzed. Additionally, the Cancer Genome Atlas dataset of patients with lung cancer was accessed. We classified adenocarcinomas using single-sample gene set enrichment analysis based on IFN-γ response pathway expression to elucidate the genomic profile and prognosis. Results: The tumor immune microenvironment is immunologically hot, with higher immune cell infiltration in the solid subtype than in the non-solid subtype. The patients were divided into two groups [Gene Ontology Biological Process-Interferon-Gamma (GOBP-IFNG) high and low] according to IFN-γ response pathway expression. In the solid subtype, the GOBP-IFNG-low group showed poorer overall survival (OS) than the GOBP-IFNG-high group. Multivariate analysis demonstrated that low GOBP-IFNG level was an independent poor prognostic factor. The apoptosis score and MHC class II expression levels were lower in the low-GOBP-IFNG group than those in the high-GOBP-IFNG group. A proliferation assay using solid subtype adenocarcinoma cell lines demonstrated that one of the three cell lines did not respond to IFN-γ. The copy number alteration (CNA) in the low-GOBP-IFNG group was higher than that in the high-GOBP-IFNG group in the solid subtype. Conclusions: Solid subtype adenocarcinomas are immunologically prevalent. IFN-γ response pathway expression is associated with the OS of solid subtype adenocarcinoma and may provide key insights to improve prognosis.

Indexed as

interferon-γ response (IFN-γ response)Lung cancertumor immune microenvironment

Identifiers

PMID41132962
PMCPMC12541845

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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.