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受体酪氨酸激酶样孤儿受体1(ROR1)在癌症干细胞信号传导中的作用

The Role of Receptor Tyrosine Kinase-like Orphan Receptor 1 (ROR1) in Cancer Stem Cell Signaling.

作者信息

Jung Matthew S, Choi Won-Young, Zhang Wenjing, Barrera Francisco N, Perkins Rachel S

机构信息

Department of Pathology, College of Medicine, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

College of Graduate Health Sciences, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

出版信息

Int J Mol Sci. 2025 Aug 13;26(16):7828. doi: 10.3390/ijms26167828.

Abstract

Receptor tyrosine kinase-like orphan receptor 1 (ROR1) is a key regulator of cancer stem cell (CSC) biology and signaling. In CSCs, ROR1 acts as a receptor or co-receptor, interacting with non-canonical WNT ligands, and forming complexes with proteins like CD19 and HER2, to activate diverse downstream signaling pathways. ROR1 signaling in CSCs promotes proliferation, maintains stemness, and enhances migration, invasion, and the epithelial-to-mesenchymal transition (EMT). While minimally expressed after embryogenesis, ROR1 is aberrantly upregulated in numerous cancers, including ovarian, breast, pancreatic, and hematologic malignancies. ROR1 overexpression drives tumor progression, resistance to chemotherapies, disease recurrence, and ultimately metastasis. This expression pattern positions ROR1 as a promising target for CSC-specific therapies. High ROR1 expression is consistently linked to aggressive disease and poor patient outcomes. Here, we review ROR1's role in CSCs and highlight the complex signaling that is observed in the CSC population. Further, we evaluate the gaps in the current understanding of ROR1 signaling in CSCs and describe how ROR1 regulates the associated signaling pathways. Finally, we provide an up-to-date summary of the promising therapeutic strategies targeting ROR1 that overcome conventional cancer treatment limitations. This review highlights the role of ROR1 as a critical, functional driver of CSCs and adverse patient outcomes across various malignancies.

摘要

受体酪氨酸激酶样孤儿受体1(ROR1)是癌症干细胞(CSC)生物学和信号传导的关键调节因子。在癌症干细胞中,ROR1作为受体或共受体,与非经典WNT配体相互作用,并与CD19和HER2等蛋白质形成复合物,以激活多种下游信号通路。癌症干细胞中的ROR1信号传导促进增殖、维持干性,并增强迁移、侵袭和上皮-间质转化(EMT)。虽然ROR1在胚胎发育后表达极低,但在包括卵巢癌、乳腺癌、胰腺癌和血液系统恶性肿瘤在内的多种癌症中异常上调。ROR1的过表达驱动肿瘤进展、化疗耐药、疾病复发,并最终导致转移。这种表达模式使ROR1成为癌症干细胞特异性治疗的一个有前景的靶点。ROR1的高表达一直与侵袭性疾病和患者预后不良相关。在这里,我们综述了ROR1在癌症干细胞中的作用,并强调了在癌症干细胞群体中观察到的复杂信号传导。此外,我们评估了目前对癌症干细胞中ROR1信号传导理解上的差距,并描述了ROR1如何调节相关信号通路。最后,我们提供了针对ROR1的有前景的治疗策略的最新总结,这些策略克服了传统癌症治疗的局限性。这篇综述强调了ROR1作为癌症干细胞的关键功能驱动因子以及在各种恶性肿瘤中对患者不良预后的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1a9/12386924/303567bdc22d/ijms-26-07828-g001.jpg

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