Endosomal recycling inhibitors downregulate the androgen receptor and synergise with enzalutamide.

IF 3 3区 医学 Q2 ONCOLOGY
Investigational New Drugs Pub Date : 2024-02-01 Epub Date: 2023-11-14 DOI:10.1007/s10637-023-01407-x
Kelsey A Fletcher, Mai H Alkurashi, Andrew J Lindsay
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引用次数: 0

Abstract

Prostate cancer is the second most frequent cancer diagnosed in men, and accounts for one-fifth of cancer associated deaths worldwide. Despite the availability of effective prostate cancer therapies, if it is not cured by radical local treatment, progression to drug resistant metastatic prostate cancer is inevitable. Therefore, new drugs and treatment regimens are urgently required to overcome resistance. We have recently published research demonstrating that targeting the endosomal recycling pathway, a membrane transport pathway that recycles internalised cell surface proteins back to the plasma membrane, may be a novel means to downregulate clinically relevant cell surface proteins and potentially overcome drug resistance. A reverse phase protein array (RPPA) assay of breast cancer cells treated with an endosomal recycling inhibitor identified the androgen receptor (AR) as one of the top downregulated proteins. We confirmed that endosomal recycling inhibitors also downregulated AR in prostate cancer cells and show that this occurs at the transcriptional level. We also found that endosomal recycling inhibitors synergise with enzalutamide, a standard-of-care therapy for prostate cancer. Our data suggest that combining recycling inhibitors with hormone receptor antagonists may enhance their efficacy and reduce the emergence of drug resistance.

Abstract Image

内体再循环抑制剂下调雄激素受体并与恩杂鲁胺协同作用。
前列腺癌是男性中第二常见的癌症,占全球癌症相关死亡人数的五分之一。尽管有有效的前列腺癌治疗方法,但如果不能通过根治性局部治疗治愈,发展为耐药转移性前列腺癌是不可避免的。因此,迫切需要新的药物和治疗方案来克服耐药性。我们最近发表的研究表明,靶向内体再循环途径(一种将内化的细胞表面蛋白再循环回质膜的膜运输途径)可能是下调临床相关细胞表面蛋白并潜在克服耐药性的新手段。用内体再循环抑制剂处理的乳腺癌细胞的逆相蛋白阵列(RPPA)检测发现雄激素受体(AR)是下调最多的蛋白之一。我们证实,内体再循环抑制剂也下调前列腺癌细胞中的AR,并表明这发生在转录水平。我们还发现内体再循环抑制剂与恩杂鲁胺协同作用,恩杂鲁胺是前列腺癌的一种标准治疗方法。我们的数据表明,将再循环抑制剂与激素受体拮抗剂联合使用可以提高其疗效并减少耐药性的出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.60
自引率
0.00%
发文量
121
审稿时长
1 months
期刊介绍: The development of new anticancer agents is one of the most rapidly changing aspects of cancer research. Investigational New Drugs provides a forum for the rapid dissemination of information on new anticancer agents. The papers published are of interest to the medical chemist, toxicologist, pharmacist, pharmacologist, biostatistician and clinical oncologist. Investigational New Drugs provides the fastest possible publication of new discoveries and results for the whole community of scientists developing anticancer agents.
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