鼻咽癌
微泡
间质细胞
生物
细胞外基质
癌症研究
基质
爱泼斯坦-巴尔病毒
转移
肿瘤进展
细胞培养
上皮-间质转换
肿瘤微环境
病理
癌症
免疫组织化学
小RNA
免疫学
病毒
细胞生物学
医学
基因
内科学
放射治疗
生物化学
遗传学
肿瘤细胞
作者
Hirotomo Dochi,Satoru Kondo,Shigetaka Komura,Makiko Moriyama‐Kita,Takeshi Komori,Asuka Nanbo,Miako Sakaguchi,Masaki Fukuyo,Toshihide Hamabe‐Horiike,Mariko Tanaka,Harue Mizokami,Makoto Kano,Yuki Kitagawa,Eiji Kobayashi,Nobuyuki Hirai,Takayoshi Ueno,Yosuke Nakanishi,Kazuhira Endo,Hisashi Sugimoto,Rikinari Hanayama
摘要
Abstract Epstein‐Barr virus (EBV)‐associated nasopharyngeal carcinoma (NPC) cells have high metastatic potential. Recent research has revealed that the interaction of between tumor cells and the surrounding stroma plays an important role in tumor invasion and metastasis. In this study, we showed the prognostic value of expression of SPARC, an extracellular matrix protein with multiple cellular functions, in normal adjacent tissues (NAT) surrounding NPC. In the immunohistochemical analysis of 51 NPC biopsy specimens, SPARC expression levels were significantly elevated in the NAT of EBER (EBV‐encoded small RNA)‐positive NPC compared to that in the NAT of EBER‐negative NPC. Moreover, increased SPARC expression in NAT was associated with a worsening of overall survival. The enrichment analysis of RNA‐seq of publicly available NPC and NAT surrounding NPC data showed that high SPARC expression in NPC was associated with epithelial mesenchymal transition promotion, and there was a dynamic change in the gene expression profile associated with interference of cellular proliferation in NAT, including SPARC expression. Furthermore, EBV‐positive NPC cells induce SPARC expression in normal nasopharyngeal cells via exosomes. Induction of SPARC in cancer‐surrounding NAT cells reduced intercellular adhesion in normal nasopharyngeal structures and promoted cell competition between cancer cells and normal epithelial cells. These results suggest that epithelial cells loosen their own binding with the extracellular matrix as well as stromal cells, facilitating the invasion of tumor cells into the adjacent stroma by activating cell competition. Our findings reveal a new mechanism by which EBV creates a pro‐metastatic microenvironment by upregulating SPARC expression in NPC.
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