工程化益生菌用于肿瘤靶向联合化学免疫治疗
Engineered probiotics for tumor-targeted combination chemoimmunotherapy.
我们的方法将酶/前药治疗和免疫治疗整合到一个单一的细菌递送系统中,通过提供合理设计的空间控制化学免疫治疗框架,克服了传统疗法的关键局限性。
英文原题:ROR1 protein: a pseudokinase at the crossroads of cancer progression and therapy.
ROR1 protein: a pseudokinase at the crossroads of cancer progression and therapy.
假激酶是人类激酶组的一个亚类,尽管缺乏酶活性,却在细胞调控中发挥关键作用。
假激酶是人类激酶组的一个亚类,尽管缺乏酶活性,仍在细胞调控中发挥关键作用。其中,受体酪氨酸激酶样孤儿受体1(ROR1)已成为癌症生物学的重要调节因子。ROR1最初因参与胚胎发育而被发现,现已知其在多种恶性肿瘤(包括血液系统癌症和实体瘤)中异常表达,而在正常成人组织中基本缺失。其独特表达模式及其在肿瘤存活、转移、治疗耐药和干性中的作用,使ROR1成为有吸引力的治疗靶点。本综述深入分析ROR1的结构和功能特征、其与致癌信号通路的相互作用及其对肿瘤进展的影响。作者还探讨了当前治疗策略,包括单克隆抗体、抗体药物偶联物(ADC)、嵌合抗原受体(CAR)T细胞疗法和小分子抑制剂,并指出其临床潜力和局限。阐明ROR1驱动致癌作用的机制并克服治疗挑战,对于开发靶向这一假激酶的有效抗癌策略至关重要。
Pseudokinases, a subclass of the human kinome, play critical roles in cellular regulation despite their lack of enzymatic activity. Among these, the Receptor Tyrosine Kinase-Like Orphan Receptor 1 (ROR1) has emerged as a pivotal regulator in cancer biology. ROR1, initially identified for its role in embryonic development, is aberrantly expressed in various malignancies, including hematologic cancers and solid tumors, while being largely absent in normal adult tissues. Its unique expression profile, coupled with its role in tumor survival, metastasis, therapy resistance, and stemness, makes ROR1 an attractive therapeutic target. This review provides an in-depth analysis of the structural and functional attributes of ROR1, its interaction with oncogenic signaling pathways, and its implications in tumor progression. We also explore current therapeutic strategies, including monoclonal antibodies, antibody-drug conjugates (ADCs), chimeric antigen receptor (CAR) T-cell therapy, and small-molecule inhibitors, highlighting their clinical potential and limitations. Understanding the mechanistic underpinnings of ROR1-driven oncogenesis and overcoming therapeutic challenges will be crucial for developing effective anti-cancer strategies targeting this pseudokinase.
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