Integrated proteomics and metabolomics analyses reveal new insights into the antitumor effects of valproic acid plus simvastatin combination in a prostate cancer xenograft model associated with downmodulation of YAP/TAZ signaling.

IF 5.3 2区 医学 Q1 ONCOLOGY Cancer Cell International Pub Date : 2024-11-16 DOI:10.1186/s12935-024-03573-1
Federica Iannelli, Rita Lombardi, Susan Costantini, Maria Serena Roca, Laura Addi, Francesca Bruzzese, Elena Di Gennaro, Alfredo Budillon, Biagio Pucci
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引用次数: 0

Abstract

Background: Despite advancements in therapeutic approaches, including taxane-based chemotherapy and androgen receptor-targeting agents, metastatic castration-resistant prostate cancer (mCRPC) remains an incurable tumor, highlighting the need for novel strategies that can target the complexities of this disease and bypass the development of drug resistance mechanisms. We previously demonstrated the synergistic antitumor interaction of valproic acid (VPA), an antiepileptic agent with histone deacetylase inhibitory activity, with the lipid-lowering drug simvastatin (SIM). This combination sensitizes mCRPC cells to docetaxel treatment both in vitro and in vivo by targeting the cancer stem cell compartment via mevalonate pathway/YAP axis modulation.

Methods: Here, using a combined proteomic and metabolomic/lipidomic approach, we characterized tumor samples derived from 22Rv1 mCRPC cell-xenografted mice treated with or without VPA/SIM and performed an in-depth bioinformatics analysis.

Results: We confirmed the specific impact of VPA/SIM on the Hippo-YAP signaling pathway, which is functionally related to the modulation of cancer-related extracellular matrix biology and metabolic reprogramming, providing further insights into the molecular mechanism of the antitumor effects of VPA/SIM.

Conclusions: In this study, we present an in-depth exploration of the potential to repurpose two generic, safe drugs for mCRPC treatment, valproic acid (VPA) and simvastatin (SIM), which already show antitumor efficacy in combination, primarily affecting the cancer stem cell compartment via MVP/YAP axis modulation. Bioinformatics analysis of the LC‒MS/MS and 1H‒NMR metabolomics/lipidomics results confirmed the specific impact of VPA/SIM on Hippo-YAP.

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蛋白质组学和代谢组学综合分析揭示了丙戊酸和辛伐他汀联合疗法在前列腺癌异种移植模型中的抗肿瘤作用与 YAP/TAZ 信号下调相关的新见解。
背景:尽管基于类固醇的化疗和雄激素受体靶向药物等治疗方法取得了进展,但转移性耐阉割前列腺癌(mCRPC)仍然是一种无法治愈的肿瘤,这凸显了人们对能够针对这种疾病的复杂性并绕过耐药机制发展的新型策略的需求。我们之前证明了丙戊酸(VPA)(一种具有组蛋白去乙酰化酶抑制活性的抗癫痫药)与降脂药辛伐他汀(SIM)的协同抗肿瘤作用。方法:在此,我们采用蛋白质组学和代谢组学/脂质组学相结合的方法,对接受或不接受VPA/SIM治疗的22Rv1 mCRPC细胞异种移植小鼠的肿瘤样本进行了表征,并进行了深入的生物信息学分析:结果:我们证实了VPA/SIM对Hippo-YAP信号通路的特定影响,而Hippo-YAP信号通路在功能上与癌症相关的细胞外基质生物学调控和代谢重编程有关,从而进一步揭示了VPA/SIM抗肿瘤作用的分子机制:在本研究中,我们深入探讨了将丙戊酸(VPA)和辛伐他汀(SIM)这两种通用安全药物重新用于mCRPC治疗的潜力,这两种药物联合使用已显示出抗肿瘤疗效,主要是通过调节MVP/YAP轴影响癌症干细胞区系。对 LC-MS/MS 和 1H-NMR 代谢组学/脂质组学结果的生物信息学分析证实了 VPA/SIM 对 Hippo-YAP 的特定影响。
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来源期刊
CiteScore
10.90
自引率
1.70%
发文量
360
审稿时长
1 months
期刊介绍: Cancer Cell International publishes articles on all aspects of cancer cell biology, originating largely from, but not limited to, work using cell culture techniques. The journal focuses on novel cancer studies reporting data from biological experiments performed on cells grown in vitro, in two- or three-dimensional systems, and/or in vivo (animal experiments). These types of experiments have provided crucial data in many fields, from cell proliferation and transformation, to epithelial-mesenchymal interaction, to apoptosis, and host immune response to tumors. Cancer Cell International also considers articles that focus on novel technologies or novel pathways in molecular analysis and on epidemiological studies that may affect patient care, as well as articles reporting translational cancer research studies where in vitro discoveries are bridged to the clinic. As such, the journal is interested in laboratory and animal studies reporting on novel biomarkers of tumor progression and response to therapy and on their applicability to human cancers.
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