Combinatorial Effect of Abiraterone Acetate and NVP-BEZ235 on Prostate Tumor Progression in Rats.

IF 3 4区 医学 Q3 Biochemistry, Genetics and Molecular Biology Hormones & Cancer Pub Date : 2018-06-01 DOI:10.1007/s12672-018-0323-z
Bianca Facchim Gonçalves, Silvana Gisele Pegorin de Campos, Wagner José Fávaro, Joyce Zalotti Brandt, Cristiane Figueiredo Pinho, Luis Antônio Justulin, Sebastião Roberto Taboga, Wellerson Rodrigo Scarano
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引用次数: 6

Abstract

Use of drug combinations that target different pathways involved in the development and progression of prostate cancer (PCa) has emerged as an alternative to overcome the resistance caused by drug monotherapies. The antiandrogen abiraterone acetate and the PI3K/Akt inhibitor NVP-BEZ235 (BEZ235) may be suitable options for the prevention of drug resistance and the inhibition of PCa progression. The aim of the present study was to evaluate whether abiraterone acetate and BEZ235 achieve superior therapeutic effects to either drug administered as monotherapy, in the early stages of PCa in an androgen-dependent system. Our study showed that each drug might impair tumor growth by reducing proliferation and increasing cell death when administered as monotherapy. However, tumor growth continued to progress with each drug monotherapy and some important side effects were related to BEZ. Conversely, when used in combination, the drugs impaired the inflammatory response, decreased hyperplastic lesions, and blocked tumor progression from premalignant to a malignant stage. Our data showed that the strategy to block the androgenic and PI3K/AKT/mTOR pathway is an effective therapeutic option and should be investigated including distinct PI3K pathway inhibitors.

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醋酸阿比特龙联合NVP-BEZ235对大鼠前列腺肿瘤进展的影响。
针对前列腺癌(PCa)发生和发展的不同途径使用药物组合已经成为克服单一药物治疗引起的耐药性的一种替代方法。抗雄激素醋酸阿比特龙和PI3K/Akt抑制剂NVP-BEZ235 (BEZ235)可能是预防耐药和抑制PCa进展的合适选择。本研究的目的是评估醋酸阿比特龙和BEZ235是否在雄激素依赖系统的早期PCa中获得优于单药治疗的治疗效果。我们的研究表明,当单药治疗时,每种药物都可能通过减少增殖和增加细胞死亡来损害肿瘤生长。然而,随着每种药物的单一治疗,肿瘤的生长持续进展,一些重要的副作用与BEZ有关。相反,当联合使用时,这些药物会削弱炎症反应,减少增生性病变,并阻止肿瘤从恶性前期发展到恶性阶段。我们的数据显示,阻断雄激素和PI3K/AKT/mTOR通路的策略是一种有效的治疗选择,应该研究包括不同的PI3K通路抑制剂。
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来源期刊
Hormones & Cancer
Hormones & Cancer ONCOLOGY-ENDOCRINOLOGY & METABOLISM
CiteScore
4.60
自引率
0.00%
发文量
0
期刊介绍: Hormones and Cancer is a unique multidisciplinary translational journal featuring basic science, pre-clinical, epidemiological, and clinical research papers. It covers all aspects of the interface of Endocrinology and Oncology. Thus, the journal covers two main areas of research: Endocrine tumors (benign & malignant tumors of hormone secreting endocrine organs) and the effects of hormones on any type of tumor. We welcome all types of studies related to these fields, but our particular attention is on translational aspects of research. In addition to basic, pre-clinical, and epidemiological studies, we encourage submission of clinical studies including those that comprise small series of tumors in rare endocrine neoplasias and/or negative or confirmatory results provided that they significantly enhance our understanding of endocrine aspects of oncology. The journal does not publish case studies.
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