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:Combination of the First-in-Class Imipridone ONC201 and Standard Anticancer Therapies as a Rational Approach for Therapeutic Benefit.
Combination of the First-in-Class Imipridone ONC201 and Standard Anticancer Therapies as a Rational Approach for Therapeutic Benefit.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
癌症治疗药物的开发面临着癌症异质性、疾病的转移性、疗效不足、毒性以及耐药性等关键挑战。这使得理解癌症的复杂性以及可成药靶点的局限性变得相当重要。ONC201(也称为dordaviprone/TIC10/Modeyso TM)是imipridone家族的首创成员,已被证明能选择性杀伤癌细胞。最近,它已获得FDA批准,成为复发性H3K27M突变型弥漫性中线胶质瘤的首个也是唯一一个治疗药物。独特的药效团、良好的治疗指数、诱导TRAIL和整合应激反应(ISR)的能力、激活NK 细胞以及穿越血脑屏障的能力是ONC201的独特特征。ONC201已显示出对不同癌症的有效性,这在许多临床前研究中已得到证实。ONC201作为单药虽然有用,但存在一些局限性,这些局限性可以通过联合策略来解决。ONC201已显示出与其他药物的协同作用,导致更大的肿瘤细胞死亡或减少肿瘤生长。下一代imipridones,即ONC206和ONC212,是ONC201更强效的类似物,并表现出相似的特征。在这篇综述中,我们讨论了ONC201及其类似物在不同癌症中采用联合策略的治疗潜力。
The development of drugs for cancer treatment faces critical challenges due to the heterogeneity in cancers, metastatic nature of the disease, lack of efficacy, toxicity, and drug resistance. This makes it quite important to understand the complexities of cancer as well as the limitations of druggable targets. ONC201 (also known as dordaviprone/TIC10/Modeyso TM ), a first-in-class member of the imipridone family, has been shown to kill cancer cells selectively. Recently, it has received FDA approval as the first and only treatment for recurrent H3K27M-mutant diffuse midline glioma. The unique pharmacophore, favorable therapeutic index, ability to induce TRAIL and the integrated stress response (ISR), activation of natural killer cells, and ability to diffuse across the blood-brain barrier are the unique characteristics of ONC201.
ONC201 has shown effectiveness against various cancers, and this has been evident in many preclinical studies. ONC201 as a single agent, although useful, has some limitations, which could be addressed by using combination strategies. ONC201 has shown synergism with other drugs, leading to greater tumor cell death or reduced tumor growth.
Next-generation imipridones, viz. ONC206 and ONC212, are more potent analogs of ONC201 and exhibit similar characteristics. In this review, we discuss the therapeutic potential of ONC201 and its analogs using combination strategies across different cancers.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
MEMBER ACCOUNT
登录成功会直接打开下一页。