Resveratrol and capsaicin as safer radiosensitizers for colorectal cancer compared to 5-fluorouracil

IF 6.9 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biomedicine & Pharmacotherapy Pub Date : 2025-02-01 DOI:10.1016/j.biopha.2024.117799
Samuel Amintas , Charles Dupin , Marie-Alix Derieppe , Isabelle Moranvillier , Isabelle Lamrissi , Corine Bourdié , Zoe Feurer , Benjamin Fernandez , Tyty Heng-Pradère , François Moreau-Gaudry , Aurélie Bedel , Véronique Vendrely , Sandrine Dabernat
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Abstract

Background and aim

Standard rectal cancer treatment includes neoadjuvant radiotherapy sensitized by 5-fluorouracil (5-FU) chemotherapy. However, 5-FU increased chemoradiotherapy response rate comes with significant toxicity, especially in older, frail patients. The development of alternatives to chemotherapy enabling radiosensitization with limited systemic toxicity is therefore needed to improve patient management. Bioactive food components (BFCs) can exhibit chemo or radio-sensitizing properties against cancer cells. Moreover, the cytotoxic action of BFCs may be tumor-specific, with reduced impact on healthy cells. We hypothesized that BFCs, in particular resveratrol and capsaicin, alone or in association, could lead to specific radio-sensitization of colorectal tumors while offering reduced toxicity compared to 5-FU.

Experimental procedure

Colorectal tumor and non-tumor cell lines were treated with resveratrol, capsaicin, or 5-FU, alone or in combination, then irradiated; survival, cell cycle, and apoptosis were analyzed. RAGγ2C−/− mice with xenografts received oral resveratrol, resveratrol + capsaicin, or 5-FU, followed by radiotherapy, with tumor growth and systemic toxicity evaluated.

Key results

Resveratrol alone or in association with capsaicin radio-potentiates colorectal tumor cells in vitro, impacting both cell cycle and apoptosis. In a preclinical mouse model, the oral administration of resveratrol and capsaicin, but not resveratrol alone, allowed the radio-sensitization of subcutaneous colorectal tumors with similar efficiency to 5-FU. Moreover, the global as well as the hematological toxicity of the BFC association was lower than those of 5-FU.

Conclusion

This work establishes BFCs as effective enhancers of radiotherapy, offering a safer alternative to traditional radiosensitization with chemotherapy.
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与5-氟尿嘧啶相比白藜芦醇和辣椒素是更安全的结直肠癌放射增敏剂。
背景与目的:标准的直肠癌治疗包括5-氟尿嘧啶(5-FU)化疗致敏的新辅助放疗。然而,5-FU增加的放化疗反应率伴随着显著的毒性,特别是对年老体弱的患者。因此,需要开发化疗的替代方案,使放射增敏与有限的全身毒性,以改善患者管理。生物活性食品成分(BFCs)可以表现出对癌细胞的化学或放射增敏特性。此外,BFCs的细胞毒性作用可能是肿瘤特异性的,对健康细胞的影响较小。我们假设BFCs,特别是白藜芦醇和辣椒素,单独或联合可导致结直肠肿瘤的特异性放射增敏,同时与5-FU相比毒性降低。实验步骤:用白藜芦醇、辣椒素或5-FU单独或联合治疗结直肠肿瘤和非肿瘤细胞系,然后照射;分析存活、细胞周期和凋亡情况。异种移植物RAGγ2C-/-小鼠分别口服白藜芦醇、白藜芦醇+ 辣椒素或5-FU,随后进行放疗,评估肿瘤生长和全身毒性。关键结果:白藜芦醇单独或与辣椒素联合可增强体外结直肠癌肿瘤细胞,影响细胞周期和凋亡。在临床前小鼠模型中,口服白藜芦醇和辣椒素,而不是白藜芦醇单独给药,可以使皮下结直肠肿瘤的放射增敏效果与5-FU相似。此外,BFC的整体毒性和血液学毒性均低于5-FU。结论:本研究确立了BFCs作为有效的放疗增强剂,为传统的放疗增敏提供了一种更安全的替代方案。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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