癌症干细胞靶向的新见解:CAR-T疗法和表观遗传学药物是癌症治疗的新支柱

Frontiers in molecular medicine Pub Date : 2023-05-18 eCollection Date: 2023-01-01 DOI:10.3389/fmmed.2023.1120090
Veronica Veschi, Alice Turdo, Giorgio Stassi
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摘要

癌症干细胞(CSCs)是肿瘤中最具攻击性的亚群,保留了侵袭能力、转移潜力和导致治疗耐药性的高表达水平的药物外排泵。癌症仍然是一种不治之症,因为标准治疗方案的无效性使这一亚群得以生存。选择性靶向CSCs仍然是癌症研究领域未满足的需求。异常的表观遗传学重编程促进CSC的启动和维持,CSC能够逃脱免疫系统的防御。能够诱导对这种干细胞样小亚群的选择性抑制的有前景的治疗方法包括单独的免疫疗法或与表观遗传化合物联合的免疫疗法。这些策略基于表位的特异性表达和/或表观遗传学改变,这些改变仅存在于CSC中,而不存在于其他癌症细胞或正常细胞中。因此,利用CAR-T免疫疗法和表观遗传学探针的联合方法可以克服治疗无效的障碍,在已知CSCs特异性改变的患者中采用更精确的药物方法。在这篇前瞻性的文章中,我们将对表观免疫疗法在富含CSCs的肿瘤中的未来应用,以及其潜在的副作用、局限性和耐药性的发展提供新的见解。
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Novel insights into cancer stem cells targeting: CAR-T therapy and epigenetic drugs as new pillars in cancer treatment.

Cancer stem cells (CSCs) represent the most aggressive subpopulation present in the tumor bulk retaining invasive capabilities, metastatic potential and high expression levels of drug efflux pumps responsible for therapy resistance. Cancer is still an incurable disease due to the inefficacy of standard regimens that spare this subpopulation. Selective targeting of CSCs is still an unmet need in cancer research field. Aberrant epigenetic reprogramming promotes the initiation and maintenance of CSCs, which are able to escape the immune system defense. Promising therapeutic approaches able to induce the selective inhibition of this stem-like small subset include immunotherapy alone or in combination with epigenetic compounds. These strategies are based on the specific expression of epitopes and/or epigenetic alterations present only in the CSC and not in the other cancer cells or normal cells. Thus, the combined approach utilizing CAR-T immunotherapy along with epigenetic probes may overcome the barriers of treatment ineffectiveness towards a more precision medicine approach in patients with known specific alterations of CSCs. In this perspective article we will shed new lights on the future applications of epi-immunotherapy in tumors enriched in CSCs, along with its potential side-effects, limitations and the development of therapy resistance.

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