Carob pod aqueous extract potentiates cisplatin efficacy and reduces toxicity in experimental hepatocellular carcinoma via mitochondrial and inflammatory pathway modulation.

IF 6.3 3区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Wael Sobhy Darwish, Abada El Sayed Khadr, Maher Abd El Naby Kamel, Tamer A Addissouky, Ahmed Zaki Ghareeb, Mabrouk A Abd Eldaim, Mohand K Razzaq, Ibrahim El Tantawy El Sayed, Hamed Mohamed Abdel-Bary, Doaa Ahmed Ghareeb
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引用次数: 0

Abstract

Background: Hepatocellular carcinoma (HCC) is a global health challenge with limited therapeutic options. The effectiveness of conventional medication like cisplatin is often compromised by their severe toxicity. This study investigated carob pod aqueous extract (CPAE), a polyphenol-rich natural product, as a potential adjunct therapy to enhance efficacy and mitigate cisplatin toxicity in a preclinical HCC animal model.

Methods: A rat model of HCC was established using diethylnitrosamine (DEN) and carbon tetrachloride (CCl₄). Forty-two Wistar rats were divided into seven groups, receiving various treatments: control, CPAE, vehicle, HCC only, HCC+CPAE, HCC+cisplatin, and HCC+CPAE+cisplatin. Liver and kidney function, metabolic profiles, oxidative stress/antioxidant parameters, gene and protein expression (AMPK, PGC-1α, TFAM, SIRT1, iNOS, NF-κB, IκK, p53, SREBP-2), histopathology, and statistical analyses were performed.

Results: HCC induction caused significant liver dysfunction, metabolic disturbances, oxidative stress, alongside dysregulation of AMPK/PGC-1α/TFAM and NF-κB/iNOS pathways. CPAE, alone or with cisplatin, markedly ameliorated these changes, improving liver and kidney function, restoring antioxidant status, reducing the tumor marker AFP, suppressing pro-inflammatory and oncogenic signaling, and enhancing histological architecture. Furthermore, Combination therapy demonstrated synergistic benefits, with CPAE reducing cisplatin-induced nephrotoxicity and enhancing its antitumor efficacy, primarily via modulation of mitochondrial biogenesis, redox balance, and inflammatory signaling.

Conclusions: CPAE exhibits potent hepatoprotective and anti-HCC activity, especially when combined with cisplatin. This combination modulates mitochondrial and inflammatory pathways while mitigating cisplatin-induced toxicity. These finding position CPAE as a promising natural adjuvant for integrative HCC management. Further translational studies are warranted to validate these findings and explore clinical applicability.

角豆豆荚水提取物通过线粒体和炎症通路调节增强顺铂疗效并降低实验性肝细胞癌的毒性。
背景:肝细胞癌(HCC)是一个全球性的健康挑战,治疗选择有限。像顺铂这样的传统药物的有效性往往因其严重的毒性而受到损害。本研究研究了角豆荚水提取物(CPAE),一种富含多酚的天然产物,作为一种潜在的辅助疗法,在临床前HCC动物模型中提高疗效并减轻顺铂毒性。方法:用二乙基亚硝胺(DEN)和四氯化碳(CCl₄)建立大鼠肝细胞癌模型。42只Wistar大鼠分为对照组、CPAE组、载药组、单纯HCC组、HCC+CPAE组、HCC+顺铂组、HCC+CPAE+顺铂组。进行肝肾功能、代谢谱、氧化应激/抗氧化参数、基因和蛋白表达(AMPK、PGC-1α、TFAM、SIRT1、iNOS、NF-κB、i -κ k、p53、SREBP-2)、组织病理学和统计学分析。结果:HCC诱导引起明显的肝功能障碍、代谢紊乱、氧化应激,同时AMPK/PGC-1α/TFAM和NF-κB/iNOS通路失调。CPAE单独或与顺铂联合使用可显著改善这些变化,改善肝肾功能,恢复抗氧化状态,降低肿瘤标志物AFP,抑制促炎和致癌信号,增强组织结构。此外,联合治疗显示出协同效益,CPAE主要通过调节线粒体生物发生、氧化还原平衡和炎症信号来降低顺铂诱导的肾毒性并增强其抗肿瘤功效。结论:CPAE具有有效的肝保护和抗hcc活性,特别是与顺铂联合使用时。这种组合调节线粒体和炎症途径,同时减轻顺铂诱导的毒性。这些发现表明CPAE是HCC综合治疗的一种很有前景的天然佐剂。需要进一步的转化研究来验证这些发现并探索临床适用性。
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来源期刊
Bioresources and Bioprocessing
Bioresources and Bioprocessing BIOTECHNOLOGY & APPLIED MICROBIOLOGY-
CiteScore
7.20
自引率
8.70%
发文量
118
审稿时长
13 weeks
期刊介绍: Bioresources and Bioprocessing (BIOB) is a peer-reviewed open access journal published under the brand SpringerOpen. BIOB aims at providing an international academic platform for exchanging views on and promoting research to support bioresource development, processing and utilization in a sustainable manner. As an application-oriented research journal, BIOB covers not only the application and management of bioresource technology but also the design and development of bioprocesses that will lead to new and sustainable production processes. BIOB publishes original and review articles on most topics relating to bioresource and bioprocess engineering, including: -Biochemical and microbiological engineering -Biocatalysis and biotransformation -Biosynthesis and metabolic engineering -Bioprocess and biosystems engineering -Bioenergy and biorefinery -Cell culture and biomedical engineering -Food, agricultural and marine biotechnology -Bioseparation and biopurification engineering -Bioremediation and environmental biotechnology
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