RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Circulating tumor cells in pancreatic cancer: more than liquid biopsy.
Circulating tumor cells in pancreatic cancer: more than liquid biopsy.
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循环肿瘤细胞(CTCs)是脱离原发灶并外渗进入血液的肿瘤细胞。通过形成CTC簇并与其他循环细胞(血小板、NK细胞、巨噬细胞等)相互作用,CTCs能够在肿瘤患者的循环系统中存活并定植于转移器官。近年来,CTCs在多种类型肿瘤的诊断、预后评估和个体化治疗中的潜力逐渐被探索,而生物技术的进步使得从患者血液样本中提取CTCs成为可能。CTCs的这些生物学特征为我们提供了关于癌症脆弱性的新见解。随着新型免疫疗法和个体化药物的出现,破坏CTCs与循环细胞之间的异型相互作用以及直接靶向CTCs具有巨大前景。胰腺癌(PC)是最恶性的癌症之一,部分原因是其早期转移、诊断困难以及治疗选择有限。尽管CTCs作为生物标志物在从诊断到治疗影响PC方面具有显著潜力,但将CTCs常规应用于PC临床管理仍面临诸多挑战。在这篇综述中,我们总结了在理解CTCs生物学特征及卓越技术进展方面所取得的进展,并提供了利用这些发展来设计未来临床工具以改善PC诊断和治疗的见解。
Circulating tumor cells (CTCs) are tumor cells that slough off the primary lesions and extravasate into the bloodstream. By forming CTC clusters and interacting with other circulating cells (platelets, NK cells, macrophage, etc.) , CTCs are able to survive in the circulatory system of tumor patients and colonize to metastatic organs. In recent years, the potential of CTCs in diagnosis, prognostic assessment, and individualized therapy of various types of tumors has been gradually explored, while advances in biotechnology have made it possible to extract CTCs from patient blood samples. These biological features of CTCs provide us with new insights into cancer vulnerabilities.
With the advent of new immunotherapies and personalized medicines, disrupting the heterotypical interaction between CTCs and circulatory cells as well as direct CTCs targeting hold great promise. Pancreatic cancer (PC) is one of the most malignant cancers, in part because of early metastasis, difficult diagnosis, and limited treatment options.
Although there is significant potential for CTCs as a biomarker to impact PC from diagnosis to therapy, there still remain a number of challenges to the routine implementation of CTCs in the clinical management of PC. In this review, we summed up the progress made in understanding biological characteristics and exceptional technological advances of CTCs and provided insight into exploiting these developments to design future clinical tools for improving the diagnosis and treatment of PC.
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