单细胞转录组测序揭示了在清细胞细胞癌的发展中异常激活的瘤细胞间信号通路
Junfeng Zhang1,2, Fuzhong Liu3, Wenjia Guo3
1Department of Urology, Xinjiang Medical University Affiliated Tumor Hospital, Urumqi, China.
异常的细胞间信号通路,特别是从分泌SPP1的癌症干细胞,驱动清细胞细胞癌 (ccRCC) 的进展. 针对这些信号可以为ccRCC提供新的治疗策略.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 癌症研究 癌症研究
背景情况:
- 异常信号通路是癌症发展和进展的关键驱动因素.
- 清细胞细胞癌 (ccRCC) 发育中的细胞间通信在很大程度上仍然没有特征.
研究的目的:
- 在ccRCC发育过程中调查异常的瘤细胞对细胞通信信号.
- 确定参与ccRCC进展的特定信号分子和途径.
主要方法:
- 从ccRCC和正常脏组织中分析单细胞RNA测序 (scRNA-seq) 数据.
- 包括子集群,副本数变异 (CNV) 分析,单细胞轨迹,细胞间通信和转录因子分析.
- 在临床样本上使用多重免疫光学验证.
主要成果:
- 在ccRCC瘤集群中发现了11个异常激活的细胞间信号通路.
- MIF和SPP1被确定为POU5F1hiCD44hiE.T癌症干细胞亚群分泌的主要信号分子.
- SPP1通过激活ILK和JAK/STAT信号通路来促进ccRCC的发展和进展.
结论:
- 异常激活的细胞间信号通路对ccRCC的发展和进展有显著的贡献.
- 一个特定的癌症干细胞亚群 (POU5F1hiCD44hiE.T) 通过异常信号分子释放和细胞间相互作用驱动恶性转变和表型发展.
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