Network-based assessment of HDAC6 activity is highly predictive of pre-clinical and clinical responses to the HDAC6 inhibitor ricolinostat

生物标志物 HDAC6型 乳腺癌 医学 临床试验 肿瘤科 体内 内科学 组蛋白脱乙酰基酶 癌症研究 药理学 癌症 生物 组蛋白 基因 生物化学 生物技术
作者
Tizita Zeleke,Qingfei Pan,Codruța Chiuzan,Maika Onishi,Mariano J. Alvarez,Erin Honan,Min Yang,Pei Ling Chia,Partha Mukhopadhyay,Sean Kelly,Ruby Wu,Kathleen Fenn,Meghna S. Trivedi,Melissa Accordino,Katherine D. Crew,Dawn L. Hershman,Matthew Maurer,Simon Jones,Andrea Califano,Kevin Kalinsky
出处
期刊:Cold Spring Harbor Laboratory - medRxiv 被引量:4
标识
DOI:10.1101/2020.04.23.20066928
摘要

ABSTRACT Despite the anticancer activity of pan-histone deacetylase (HDAC) inhibitors, their clinical use has been limited due to toxicity. However, the development of more specific inhibitors that selectively inhibit individual HDACs is emerging as a novel and well-tolerated alternative. Here, we present the results of the first clinical trial evaluating the activity of ricolinostat (the leading HDAC6 inhibitor) in breast cancer (BC) patients. We have developed a computational network-based algorithm to evaluate the activity of the HDAC6 protein, based on the enrichment of its transcriptional targets in differentially expressed genes (HDAC6 score). Through preclinical in vitro and in vivo studies, we confirmed that the HDAC6 score can stratify the sensitivity of BC cells to ricolinostat treatment and may thus have value as a predictive biomarker. Moreover, analysis of ∼3,000 primary human breast cancers showed that ∼30% of them present high HDAC6 scores. Based on these results, we designed a phase Ib clinical trial to evaluate the activity of ricolinostat plus nab-paclitaxel in metastatic BC patients. Study results showed that the two agents can be safely combined, that clinical activity is identified specifically in patients with HR+/HER2-disease, and that the HDAC6 score was predictive of response. Expansion of our analysis to other tumor types identified multiple cohorts enriched in high HDAC6 score samples. These results suggest that the HDAC6 score may provide an effective, CLIA certified predictive biomarker of ricolinostat sensitivity in multiple human cancers. SIGNIFICANCE The clinical use of HDAC inhibitors is hampered by the toxicity associated with blocking multiple HDACs. Here, we show that the specific HDAC6 inhibitor ricolinostat is safe and presents clinical activity in breast cancers and that the HDAC6 score has predictive biomarker potential to identify patients who can benefit from this therapy.
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