综合单细胞和批量转录组分析揭示了乳腺癌和甲状腺癌的共享病原和预后生物标志物
Bingbing Shen1,2, Jiayi Jiang3, Xinyue Zhang4
1Division of Thyroid Surgery, Department of General Surgery, Laboratory of Thyroid and Parathyroid Diseases, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Chengdu, China.
Frontiers in immunology
|January 28, 2026
概括
这项研究揭示了乳腺癌 (BC) 和甲状腺癌 (TC) 之间的共享分子通路,包括JAK-STAT信号传输. SMR3B被确定为这些相关恶性瘤的关键预后生物标志物和治疗标.
科学领域:
- 在瘤学瘤学.
- 生物信息学是一种生物信息学.
- 分子生物学分子生物学
背景情况:
- 乳腺癌 (BC) 和甲状腺癌 (TC) 是激素调控的恶性瘤,并随之增加.
- 它们的共同发生背后的分子机制尚不清楚.
研究的目的:
- 为了阐明BC和TC之间的共享病原体.
- 为两种癌症确定共同的预后生物标志物和治疗点.
主要方法:
- 单细胞和大量RNA测序数据的综合生物信息学分析.
- 进行了功能丰富,单细胞转录组,CNV,NMF和WGCNA分析.
- 使用机器学习和功能测试进行验证的预测签名构建.
主要成果:
- 确定了JAK-STAT信号通路和细胞因子-细胞因子受体相互作用作为共享的致病机制.
- 关键的基因表达模块 (MP2,MP4,MP5) 和细胞群 (SFRP2+纤维细胞,HLA_DPB1+髓状细胞) 在两种癌症中都至关重要.
- SMR3B被验证为一种共同的预后基因,影响繁殖,迁移和入侵.
结论:
- 对BC和TC的共同分子机制的全面见解.
- SMR3B是一种有前途的预后生物标志物和双重风险患者的治疗标.
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