针对化疗耐药三阴性乳腺癌的奈德酰化和苏木酰化。

IF 6.5 2区 医学 Q1 ONCOLOGY
Reid T Powell, Amanda L Rinkenbaugh, Lei Guo, Shirong Cai, Jiansu Shao, Xinhui Zhou, Xiaomei Zhang, Sabrina Jeter-Jones, Chunxiao Fu, Yuan Qi, Faiza Baameur Hancock, Jason B White, Clifford Stephan, Peter J Davies, Stacy Moulder, W Fraser Symmans, Jeffrey T Chang, Helen Piwnica-Worms
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引用次数: 0

摘要

在美国,三阴性乳腺癌(TNBC)占乳腺癌病例的 15-20%。全身新辅助化疗(NACT)联合或不联合免疫疗法是目前治疗早期 TNBC 患者的标准疗法。然而,多达 70% 的 TNBC 患者在完成新辅助化疗后会有明显的疾病残留,这与手术切除后两到三年内复发的高风险有关。为了确定化疗耐药 TNBC 的可靶向漏洞,我们在患者接受 NACT 之前和之后从 TNBC 肿瘤中生成了纵向患者衍生异种移植 (PDX) 模型。然后,我们汇编了所有模型的转录组和药物反应谱。转录组分析发现,与接受 NACT 治疗前的肿瘤相比,接受 NACT 治疗后的肿瘤模型中异常蛋白稳态通路更为丰富。这一观察结果与体外靶向蛋白酶体、热休克蛋白和内酰化途径的抑制剂的敏感性增加有关。Pevonedistat是一种注释为NEDD8激活酶(NAE)抑制剂的药物,被优先用于体内验证,并在多个TNBC PDX模型中显示出单药疗效。药物转录组学分析确定了培伐尼司他的活性与翻译后修饰(PTM)机制之间的通路级相关性,特别是涉及neddylation和sumoylation靶点的相关性。与体内反应较差的模型相比,在对培伐尼司他反应良好的模型中观察到 NEDD8 和 SUMO1 水平升高。此外,Neddylation调控通路的表达与肿瘤对培伐尼司他的反应之间存在相关性,这表明靶向这些PTM通路可能会被证明是对抗化疗耐药TNBC的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targeting neddylation and sumoylation in chemoresistant triple negative breast cancer.

Targeting neddylation and sumoylation in chemoresistant triple negative breast cancer.

Triple negative breast cancer (TNBC) accounts for 15-20% of breast cancer cases in the United States. Systemic neoadjuvant chemotherapy (NACT), with or without immunotherapy, is the current standard of care for patients with early-stage TNBC. However, up to 70% of TNBC patients have significant residual disease once NACT is completed, which is associated with a high risk of developing recurrence within two to three years of surgical resection. To identify targetable vulnerabilities in chemoresistant TNBC, we generated longitudinal patient-derived xenograft (PDX) models from TNBC tumors before and after patients received NACT. We then compiled transcriptomes and drug response profiles for all models. Transcriptomic analysis identified the enrichment of aberrant protein homeostasis pathways in models from post-NACT tumors relative to pre-NACT tumors. This observation correlated with increased sensitivity in vitro to inhibitors targeting the proteasome, heat shock proteins, and neddylation pathways. Pevonedistat, a drug annotated as a NEDD8-activating enzyme (NAE) inhibitor, was prioritized for validation in vivo and demonstrated efficacy as a single agent in multiple PDX models of TNBC. Pharmacotranscriptomic analysis identified a pathway-level correlation between pevonedistat activity and post-translational modification (PTM) machinery, particularly involving neddylation and sumoylation targets. Elevated levels of both NEDD8 and SUMO1 were observed in models exhibiting a favorable response to pevonedistat compared to those with a less favorable response in vivo. Moreover, a correlation emerged between the expression of neddylation-regulated pathways and tumor response to pevonedistat, indicating that targeting these PTM pathways may prove effective in combating chemoresistant TNBC.

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来源期刊
NPJ Breast Cancer
NPJ Breast Cancer Medicine-Pharmacology (medical)
CiteScore
10.10
自引率
1.70%
发文量
122
审稿时长
9 weeks
期刊介绍: npj Breast Cancer publishes original research articles, reviews, brief correspondence, meeting reports, editorial summaries and hypothesis generating observations which could be unexplained or preliminary findings from experiments, novel ideas, or the framing of new questions that need to be solved. Featured topics of the journal include imaging, immunotherapy, molecular classification of disease, mechanism-based therapies largely targeting signal transduction pathways, carcinogenesis including hereditary susceptibility and molecular epidemiology, survivorship issues including long-term toxicities of treatment and secondary neoplasm occurrence, the biophysics of cancer, mechanisms of metastasis and their perturbation, and studies of the tumor microenvironment.
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