肿瘤进展
间质细胞
生物
病理
纤维化
血管生成
转录组
恶性转化
癌症研究
细胞
基质
免疫系统
癌症
医学
免疫学
免疫组织化学
基因
基因表达
遗传学
生物化学
作者
Liang Zhong,Fei Wang,Dan Liu,Wenjing Kuang,Ning Ji,Jing Li,Xin Zeng,Taiwen Li,Hongxia Dan,Qianming Chen
摘要
Abstract Objective Proliferative verrucous leukoplakia (PVL) is characterized by a spectrum of clinicopathological features and a high risk of malignant transformation. In this study, we aimed to delineate the dynamic changes in molecular signature during PVL progression and identify the potential cell subtypes that play a key role in the premalignant evolution of PVL. Methods We performed single‐cell RNA sequencing on three biopsy samples from a large PVL lesion. These samples exhibited a histopathological continuum of PVL progression. Results By analyzing the transcriptome profiles of 27,611 cells from these samples, we identified ten major cell lineages and revealed that cellular remodeling occurred during the progression of PVL lesions, including epithelial, stromal, and immune cells. Epithelial cells are shifted to tumorigenic states and secretory patterns at the premalignant stage. Immune cells showed growing immunosuppressive phenotypes during PVL progression. Remarkably, two novel cell subtypes INSR + endothelial cells and ASPN + fibroblasts, were discovered and may play vital roles in microenvironment remodeling, such as angiogenesis and stromal fibrosis, which are closely involved in malignant transformation. Conclusion Our work is the first to depict the cellular landscape of PVL and speculate that disease progression may be driven by functional remodeling of multiple cell subtypes.
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