한빛사논문
- 조회264
Hyewon Chung1,2, Park Gyu-mi1,3, Yi Rang Na4, Yun-Sang Lee5,6, Hongyoon Choi5,6, Seung Hyeok Seok1,3,7
1Macrophage Lab, Department of Microbiology and Immunology, and Institute of Endemic Disease, Seoul National University College of Medicine, Seoul 110-799, South Korea.
2Institute of Endemic Diseases, Seoul National University Medical Research Center (SNUMRC), Seoul, Republic of Korea.
3Department of Biomedical Sciences and Seoul National University College of Medicine, Seoul, Republic of Korea.
4Transdisciplinary Department of Medicine and Advanced Technology, Seoul National University Hospital, Seoul, South Korea.
5Department of Nuclear Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
6Department of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
7Cancer Research Institute, Seoul National University, Seoul, South Korea.
Corresponding authors: Hongyoon Choi, M.D., Ph.D.; Seung Hyeok Seok, DVM, Ph.D.
Abstract
Background: In recent years, there has been considerable interest in the therapeutic targeting of tumor-associated macrophages (TAMs) to modulate the tumor microenvironment (TME), resulting in antitumoral phenotypes. However, key mediators suitable for TAM-mediated remodeling of the TME remain poorly understood.
Methods: In this study, we used single-cell RNA sequencing analyses to analyze the landscape of the TME modulated by TAMs in terms of a protumor microenvironment during early tumor development.
Results: Our data revealed that the depletion of TAMs leads to a decreased epithelial-to-mesenchymal transition (EMT) signature in cancer cells and a distinct transcriptional state characterized by CD8+ T cell activation. Moreover, notable alterations in gene expression were observed upon the depletion of TAMs, identifying Galectin-1 (Gal-1) as a crucial molecular factor responsible for the observed effect. Gal-1 inhibition reversed immune suppression via the reinvigoration of CD8+ T cells, impairing tumor growth and potentiating immune checkpoint inhibitors in breast tumor models.
Conclusion: These results provide comprehensive insights into TAM-mediated early tumor microenvironments and reveal immune evasion mechanisms that can be targeted by Gal-1 to induce antitumor immune responses.
논문정보
- Research article
- 2024년 01월 (BRIC 등록일 2024-01-04)
- 국내 연구진
- 의약학 > 면역의학
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