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Single-cell transcriptome analysis reveals the potential heterogeneous mechanism of CD8 T cell immune dysfunction in thyroid cancer.

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Scientific reports 📖 저널 OA 98.8% 2021: 24/24 OA 2022: 32/32 OA 2023: 45/45 OA 2024: 140/140 OA 2025: 938/938 OA 2026: 738/767 OA 2021~2026 2025 Vol.15(1) p. 35861
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Zhang Q, Song K, Li C, Song X, Zhou J

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Anaplastic thyroid cancer (ATC) and papillary thyroid carcinoma (PTC) exhibit significant differences in clinical behavior and immune microenvironments, particularly concerning the mechanisms underlyi

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APA Zhang Q, Song K, et al. (2025). Single-cell transcriptome analysis reveals the potential heterogeneous mechanism of CD8 T cell immune dysfunction in thyroid cancer.. Scientific reports, 15(1), 35861. https://doi.org/10.1038/s41598-025-19995-4
MLA Zhang Q, et al.. "Single-cell transcriptome analysis reveals the potential heterogeneous mechanism of CD8 T cell immune dysfunction in thyroid cancer.." Scientific reports, vol. 15, no. 1, 2025, pp. 35861.
PMID 41087654 ↗

Abstract

Anaplastic thyroid cancer (ATC) and papillary thyroid carcinoma (PTC) exhibit significant differences in clinical behavior and immune microenvironments, particularly concerning the mechanisms underlying CD8 T cell dysfunction. However, these specific mechanisms have yet to be thorThe original blots and abbreviations are presented in Supplemeoughly investigated. The present study utilized single-cell RNA sequencing (scRNA-seq) data to conduct a comprehensive analysis of CD8 T cells in the thyroid tissues of patients diagnosed with ATC and PTC. The results of the study indicate that CD8 T cells in ATC display disruptions in energy supply and marked signs of exhaustion. Conversely, CD8 T cells in PTC are more prone to maintaining a stable expression of immunosuppression-related membrane proteins through posttranslational modifications. This study highlights the distinct mechanisms of CD8 T cell exhaustion in two types of thyroid cancer, offering valuable insights into the regulation of their immune microenvironments.

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