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ATX-101 是一种靶向 PCNA 的穿膜蛋白,可作为静脉输注药物在患者中安全给药,并在 1 期研究中显示出临床活性。

ATX-101, a cell-penetrating protein targeting PCNA, can be safely administered as intravenous infusion in patients and shows clinical activity in a Phase 1 study.

机构信息

Scientia Clinical Research, Randwick, Australia and Prince of Wales Clinical School, UNSW Sydney, Sydney, NSW, Australia.

Southern Oncology Clinical Research Unit, Bedford Park, SA, Australia.

出版信息

Oncogene. 2023 Feb;42(7):541-544. doi: 10.1038/s41388-022-02582-6. Epub 2022 Dec 23.

DOI:10.1038/s41388-022-02582-6
PMID:36564469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9918429/
Abstract

Proliferating Cell Nuclear Antigen (PCNA) is a highly conserved protein essential for DNA replication, repair and scaffold functions in the cytosol. Specific inhibition of PCNA in cancer cells is an attractive anti-cancer strategy. ATX-101 is a first-in-class drug targeting PCNA, primarily in cellular stress regulation. Multiple in vivo and in vitro investigations demonstrated anti-cancer activity of ATX-101 in many tumor types and a potentiating effect on the activity of anti-cancer therapies. Healthy cells were less affected. Based on preclinical data, a clinical phase 1 study was initiated. Twenty-five patients with progressive, late-stage solid tumors were treated with weekly ATX-101 infusions at four dose levels (20, 30, 45, 60 mg/m). ATX-101 showed a favorable safety profile supporting that vital cellular functions are not compromised in healthy cells. Mild and moderate infusion-related reactions were observed in 64% of patients. ATX-101 was quickly cleared from blood with elimination half-lives of less than 30 min at all dose levels, probably due to both, a quick cell penetration and peptide digestion in serum, as demonstrated in vivo. No tumor responses were observed but stable disease was seen in 70% of the efficacy population (n = 20). Further studies have been initiated to provide evidence of efficacy. Trial registration numbers: ANZCTR 375262 and ANZCTR 375319.

摘要

增殖细胞核抗原(PCNA)是一种高度保守的蛋白质,对于细胞质中的 DNA 复制、修复和支架功能至关重要。在癌细胞中特异性抑制 PCNA 是一种有吸引力的抗癌策略。ATX-101 是一种针对 PCNA 的首创药物,主要用于细胞应激调节。多项体内和体外研究表明,ATX-101 在多种肿瘤类型中具有抗癌活性,并增强了抗癌疗法的活性。健康细胞受影响较小。基于临床前数据,启动了一项临床 I 期研究。25 名患有进展期晚期实体瘤的患者接受每周一次 ATX-101 输注,剂量水平为 4 个(20、30、45、60mg/m)。ATX-101 表现出良好的安全性特征,支持健康细胞中的重要细胞功能不受影响。64%的患者观察到轻度和中度输注相关反应。ATX-101 从血液中快速清除,所有剂量水平的消除半衰期均小于 30 分钟,这可能是由于细胞快速穿透和血清中肽的消化,如体内研究所示。未观察到肿瘤反应,但疗效人群(n=20)中 70%的患者疾病稳定。已启动进一步的研究以提供疗效证据。试验注册号:ANZCTR 375262 和 ANZCTR 375319。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8141/9918429/26dec16c0c5f/41388_2022_2582_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8141/9918429/26dec16c0c5f/41388_2022_2582_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8141/9918429/26dec16c0c5f/41388_2022_2582_Fig1_HTML.jpg

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