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单细胞 RNA 测序揭示了与上尿路上皮癌发生和转移相关的肿瘤微环境异质性。

ScRNA-seq revealed the tumor microenvironment heterogeneity related to the occurrence and metastasis in upper urinary tract urothelial carcinoma.

机构信息

Department of Urology, Shanghai East Hospital, School of Medicine, Tongji University, Shanghai, 200120, China.

Department of Urology, The First Affiliated Hospital and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471000, China.

出版信息

Cancer Gene Ther. 2024 Aug;31(8):1201-1220. doi: 10.1038/s41417-024-00779-3. Epub 2024 Jun 14.

Abstract

Metastasis is the greatest clinical challenge for UTUCs, which may have distinct molecular and cellular characteristics from earlier cancers. Herein, we provide single-cell transcriptome profiles of UTUC para cancer normal tissue, primary tumor lesions, and lymphatic metastases to explore possible mechanisms associated with UTUC occurrence and metastasis. From 28,315 cells obtained from normal and tumor tissues of 3 high-grade UTUC patients, we revealed the origin of UTUC tumor cells and the homology between metastatic and primary tumor cells. Unlike the immunomicroenvironment suppression of other tumors, we found no immunosuppression in the tumor microenvironment of UTUC. Moreover, it is imperative to note that stromal cells are pivotal in the advancement of UTUC. This comprehensive single-cell exploration enhances our comprehension of the molecular and cellular dynamics of metastatic UTUCs and discloses promising diagnostic and therapeutic targets in cancer-microenvironment interactions.

摘要

转移是 UTUC 面临的最大临床挑战,其可能具有与早期癌症不同的分子和细胞特征。在此,我们提供 UTUC 癌旁正常组织、原发肿瘤病变和淋巴转移的单细胞转录组图谱,以探索与 UTUC 发生和转移相关的可能机制。从 3 名高级别 UTUC 患者的正常和肿瘤组织中获得的 28315 个细胞中,我们揭示了 UTUC 肿瘤细胞的起源以及转移和原发肿瘤细胞之间的同源性。与其他肿瘤的免疫微环境抑制不同,我们在 UTUC 的肿瘤微环境中没有发现免疫抑制。此外,值得注意的是,间质细胞在 UTUC 的进展中起着关键作用。这种全面的单细胞探索增强了我们对转移性 UTUC 的分子和细胞动力学的理解,并揭示了癌症-微环境相互作用中具有前景的诊断和治疗靶点。

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