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Multicellular ecotypes shape progression of lung adenocarcinoma from ground-glass opacity toward advanced stages.

Authors :
Deng Y
Xia L
Zhang J
Deng S
Wang M
Wei S
Li K
Lai H
Yang Y
Bai Y
Liu Y
Luo L
Yang Z
Chen Y
Kang R
Gan F
Pu Q
Mei J
Ma L
Lin F
Guo C
Liao H
Zhu Y
Liu Z
Liu C
Hu Y
Yuan Y
Zha Z
Yuan G
Zhang G
Chen L
Cheng Q
Shen S
Liu L
Source :
Cell reports. Medicine [Cell Rep Med] 2024 Apr 16; Vol. 5 (4), pp. 101489. Date of Electronic Publication: 2024 Mar 29.
Publication Year :
2024

Abstract

Lung adenocarcinoma is a type of cancer that exhibits a wide range of clinical radiological manifestations, from ground-glass opacity (GGO) to pure solid nodules, which vary greatly in terms of their biological characteristics. Our current understanding of this heterogeneity is limited. To address this gap, we analyze 58 lung adenocarcinoma patients via machine learning, single-cell RNA sequencing (scRNA-seq), and whole-exome sequencing, and we identify six lung multicellular ecotypes (LMEs) correlating with distinct radiological patterns and cancer cell states. Notably, GGO-associated neoantigens in early-stage cancers are recognized by CD8 <superscript>+</superscript> T cells, indicating an immune-active environment, while solid nodules feature an immune-suppressive LME with exhausted CD8 <superscript>+</superscript> T cells, driven by specific stromal cells such as CTHCR1 <superscript>+</superscript> fibroblasts. This study also highlights EGFR(L858R) neoantigens in GGO samples, suggesting potential CD8 <superscript>+</superscript> T cell activation. Our findings offer valuable insights into lung adenocarcinoma heterogeneity, suggesting avenues for targeted therapies in early-stage disease.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2666-3791
Volume :
5
Issue :
4
Database :
MEDLINE
Journal :
Cell reports. Medicine
Publication Type :
Academic Journal
Accession number :
38554705
Full Text :
https://doi.org/10.1016/j.xcrm.2024.101489