利用蜂胶及其多酚/类黄酮化合物与化疗和放疗相结合克服抗药性途径的潜在策略。

IF 4.8 2区 医学 Q1 NUTRITION & DIETETICS
Nutrients Pub Date : 2024-10-31 DOI:10.3390/nu16213741
Nada Oršolić, Maja Jazvinšćak Jembrek
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引用次数: 0

摘要

传统的癌症治疗方法包括手术切除、化疗、热疗、免疫疗法、激素疗法以及放疗等局部靶向疗法。标准的癌症疗法通常需要使用多种药物,这可能会激活肿瘤细胞中的核因子卡巴B(NF-κB),导致细胞死亡减少和耐药性增强。此外,使用多种药物还会增加毒性,导致治疗效果不佳。癌细胞通过各种机制逐渐对几乎所有化疗药物产生耐药性,如药物外流、药物代谢和转运改变、信号转导通路改变、DNA 修复能力增强、逃避凋亡、突变增加、药物靶点重新激活、与癌症微环境相互作用、癌细胞-间质相互作用、上皮-间质转化(EMT)介导的化疗耐药性、表观遗传修饰、代谢改变以及癌症干细胞(CSCs)的影响。要取得更好的治疗效果并提高患者的生活质量,就必须开发新的策略来提高化疗的敏感性,同时最大限度地减少副作用。一种很有前景的方法是将传统的癌症治疗方法与蜂胶及其黄酮类化合物相结合。这些天然化合物可增强肿瘤对治疗的反应,同时降低毒性。蜂胶及其成分可使癌细胞对化疗药物敏感,这可能是通过抑制NF-κB活化、重编程肿瘤相关巨噬细胞(TAMs;一种类似M2的表型),从而减少基质金属蛋白酶(MMP)-9、细胞因子、趋化因子和血管内皮生长因子(VEGF)的释放。通过减少TAMs,蜂胶及其成分还可以克服EMT介导的化疗抗性,破坏巨噬细胞和CSCs之间的串联,抑制干性的维持,逆转获得性免疫抑制,从而促进细胞毒性T细胞介导的抗肿瘤反应。这篇综述强调了类黄酮调节癌症对传统治疗方式反应的潜力。有证据表明,可以开发出结合类黄酮的新型治疗策略,以改善治疗效果。蜂胶与化疗药物结合的积极作用包括降低对外周血白细胞、肝脏和肾脏细胞的细胞毒性。因此,多酚/类黄酮成分在临床治疗各类癌症中与化疗药物结合使用可能具有潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential Strategies for Overcoming Drug Resistance Pathways Using Propolis and Its Polyphenolic/Flavonoid Compounds in Combination with Chemotherapy and Radiotherapy.

Conventional cancer treatments include surgical resection, chemotherapy, hyperthermia, immunotherapy, hormone therapy, and locally targeted therapies such as radiation therapy. Standard cancer therapies often require the use of multiple agents, which can activate nuclear factor kappa B (NF-κB) in tumor cells, leading to reduced cell death and increased drug resistance. Moreover, the use of multiple agents also contributes to added toxicity, resulting in poor treatment outcomes. Cancer cells gradually develop resistance to almost all chemotherapeutics through various mechanisms, such as drug efflux, alterations in drug metabolism and transport, changes in signal transduction pathways, enhanced DNA repair capacity, evasion of apoptosis, increased mutations, reactivation of drug targets, interaction with the cancer microenvironment, cancer cell-stroma interactions, epithelial-mesenchymal transition (EMT)-mediated chemoresistance, epigenetic modifications, metabolic alterations, and the effect of cancer stem cells (CSCs). Developing new strategies to improve chemotherapy sensitivity while minimizing side effects is essential for achieving better therapeutic outcomes and enhancing patients' quality of life. One promising approach involves combining conventional cancer treatments with propolis and its flavonoids. These natural compounds may enhance tumor response to treatment while reducing toxicity. Propolis and its components can sensitize cancer cells to chemotherapeutic agents, likely by inhibiting NF-κB activation, reprogramming tumor-associated macrophages (TAMs; an M2-like phenotype), and thereby reducing the release of matrix metalloproteinase (MMP)-9, cytokines, chemokines, and the vascular endothelial growth factor (VEGF). By reducing TAMs, propolis and its components may also overcome EMT-mediated chemoresistance, disrupt the crosstalk between macrophages and CSCs, inhibit the maintenance of stemness, and reverse acquired immunosuppression, thus promoting an antitumor response mediated by cytotoxic T-cells. This review highlights the potential of flavonoids to modulate the responsiveness of cancer to conventional treatment modalities. The evidence suggests that novel therapeutic strategies incorporating flavonoids could be developed to improve treatment outcomes. The positive effects of combining propolis with chemotherapeutics include reduced cytotoxicity to peripheral blood leukocytes, liver, and kidney cells. Therefore, polyphenolic/flavonoid components may hold potential for use in combination with chemotherapeutic agents in the clinical treatment of various types of cancers.

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来源期刊
Nutrients
Nutrients NUTRITION & DIETETICS-
CiteScore
9.20
自引率
15.30%
发文量
4599
审稿时长
16.74 days
期刊介绍: Nutrients (ISSN 2072-6643) is an international, peer-reviewed open access advanced forum for studies related to Human Nutrition. It publishes reviews, regular research papers and short communications. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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