CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Rethinking cancer targeting strategies in the era of smart cell therapeutics.
Rethinking cancer targeting strategies in the era of smart cell therapeutics.
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在过去的几十年里,癌症治疗的发展主要集中于对单一癌症相关分子的精准靶向。尽管取得了巨大进展,这类靶向治疗仍表现出不完全的精准性,并最终因靶点异质性或突变而产生耐药。
然而,近年来基于细胞的疗法(如嵌合抗原受体(CAR)T细胞)的发展提供了一个革命性的机会,可重新构建靶向癌症的策略。配备合成回路的免疫细胞本质上是活体计算机,可被编程为基于多种信号识别肿瘤,这些信号既包括肿瘤细胞内在信号,也包括微环境信号。
此外,细胞可被编程为启动广泛但高度局部化的治疗反应,从而在保持高精准性的同时限制逃逸的可能性。尽管这些新兴的智能细胞工程能力尚未在临床中充分实现,但我们在此认为,当它们与基因组数据的机器学习分析相结合时,将变得更加强大,因为后者可以指导最具区分度和可操作性的治疗性识别程序的设计。癌症分析与合成生物学的融合可能带来更精细的肿瘤识别范式,更类似于面部识别,从而能够更有效地应对癌症治疗中的复杂挑战。
In the past several decades, the development of cancer therapeutics has largely focused on precision targeting of single cancer-associated molecules. Despite great advances, such targeted therapies still show incomplete precision and the eventual development of resistance due to target heterogeneity or mutation.
However, the recent development of cell-based therapies such as chimeric antigen receptor (CAR) T cells presents a revolutionary opportunity to reframe strategies for targeting cancers. Immune cells equipped with synthetic circuits are essentially living computers that can be programmed to recognize tumours based on multiple signals, including both tumour cell-intrinsic and microenvironmental.
Moreover, cells can be programmed to launch broad but highly localized therapeutic responses that can limit the potential for escape while still maintaining high precision. Although these emerging smart cell engineering capabilities have yet to be fully implemented in the clinic, we argue here that they will become much more powerful when combined with machine learning analysis of genomic data, which can guide the design of therapeutic recognition programs that are the most discriminatory and actionable.
The merging of cancer analytics and synthetic biology could lead to nuanced paradigms of tumour recognition, more akin to facial recognition, that have the ability to more effectively address the complex challenges of treating cancer.
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