한빛사논문
Ji-Hye Choi1,2,6, Bok-Soon Lee3,6, Jeon Yeob Jang2,3,6, Yun Sang Lee3, Hyo Jeong Kim3,4, Jin Roh5, Yoo Seob Shin3, Hyun Goo Woo1,2 & Chul-Ho Kim3,5
1Departent of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea.
2Department of Biomedical Science, Graduate School, Ajou University, Suwon, Republic of Korea.
3Department of Otolaryngology, Ajou University School of Medicine, Suwon, Republic of Korea.
4Department of Molecular Science and Technology, Ajou University, Suwon, Republic of Korea.
5Department of Pathology, Ajou University School of Medicine, Suwon, Republic of Korea.
6These authors contributed equally: Ji-Hye Choi, Bok-Soon Lee, Jeon Yeob Jang.
Corresponding authors : Correspondence to Hyun Goo Woo or Chul-Ho Kim.
Abstract
Head and neck squamous cell carcinoma (HNSCC) undergoes stepwise progression from normal tissues to precancerous leukoplakia, primary HNSCC, and metastasized tumors. To delineate the heterogeneity of tumor cells and their interactions during the progression of HNSCC, we employ single-cell RNA-seq profiling for normal to metastasized tumors. We can identify the carcinoma in situ cells in leukoplakia lesions that are not detected by pathological examination. In addition, we identify the cell type subsets of the Galectin 7B (LGALS7B)-expressing malignant cells and CXCL8-expressing fibroblasts, demonstrating that their abundance in tumor tissue is associated with unfavorable prognostic outcomes. We also demonstrate the interdependent ligand-receptor interaction of COL1A1 and CD44 between fibroblasts and malignant cells, facilitating HNSCC progression. Furthermore, we report that the regulatory T cells in leukoplakia and HNSCC tissues express LAIR2, providing a favorable environment for tumor growth. Taken together, our results update the pathobiological insights into cell-cell interactions during the stepwise progression of HNSCCs.
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