CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Therapeutic Role of Carotenoids in Blood Cancer: Mechanistic Insights and Therapeutic Potential.
Therapeutic Role of Carotenoids in Blood Cancer: Mechanistic Insights and Therapeutic Potential.
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血液癌症的特征是导致造血细胞不受控制分裂的病理性疾病。此前已探索了多种治疗血液癌症的策略,包括化疗、CAR-T 疗法、靶向嵌合抗原受体以及血小板疗法。
然而,所有这些疗法都面临严重挑战,限制了它们在血液癌症治疗中的应用,例如代谢不良。此外,抗癌药物的溶解性和稳定性限制了疗效和生物分布,并导致毒性。在CAR-T 细胞治疗过程中,NK 细胞的分离和纯化是一个主要挑战。为应对这些挑战,来自植物药物支架的治疗策略已被评估用于血液癌症治疗。类胡萝卜素代表了一类多功能的植物化学物质,在癌症尤其是血液癌症的治疗中具有治疗效力。类胡萝卜素通过各种信号通路和机制,例如激活AMPK、表达自噬生化标志物(p62/LC3-II)、激活Keap1-Nrf2/EpRE/ARE信号通路、核因子κ轻链增强子活化B细胞(NF-κB)、活性氧水平升高、裂解的聚(ADP-核糖)聚合酶(c-PARP)、c-caspase-3、-7、Bcl-xL水平降低、细胞周期阻滞于G0/G1期以及降低STAT3表达,从而诱导凋亡并抑制癌细胞增殖。本综述文章聚焦类胡萝卜素在血液癌症中的治疗潜力,探讨介导其治疗效力的各种机制和信号通路。
Blood cancers are characterized by pathological disorders causing uncontrolled hematological cell division. Various strategies were previously explored for the treatment of blood cancers, including chemotherapy, Car-T therapy, targeting chimeric antigen receptors, and platelets therapy.
However, all these therapies pose serious challenges that limit their use in blood cancer therapy, such as poor metabolism.
Furthermore, the solubility and stability of anticancer drugs limit efficacy and bio-distribution and cause toxicity. The isolation and purification of natural killer cells during Car-T cell therapy is a major challenge. To cope with these challenges, treatment strategies from phyto-medicine scaffolds have been evaluated for blood cancer treatments. Carotenoids represent a versatile class of phytochemical that offer therapeutic efficacy in the treatment of cancer, and specifically blood cancer.
Carotenoids, through various signaling pathways and mechanisms, such as the activation of AMPK, expression of autophagy biochemical markers (p62/LC3-II), activation of Keap1-Nrf2/EpRE/ARE signaaling pathway, nuclear factor kappa-light-chain-enhancer of activated B cells (NF- B), increased level of reactive oxygen species, cleaved poly (ADP-ribose) polymerase (c-PARP), c-caspase-3, -7, decreased level of Bcl-xL, cycle arrest at the G0/G1 phase, and decreasing STAT3 expression results in apoptosis induction and inhibition of cancer cell proliferation.
This review article focuses the therapeutic potential of carotenoids in blood cancers, addressing various mechanisms and signaling pathways that mediate their therapeutic efficacy.
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