他玛西汀通过靶向dpp7介导的WNT3A/β-Catenin信号通路抑制结直肠癌进展

IF 4.2
Peng Ouyang, Jin Gong, Jinlin Nie, Sridhar Kandala, Yangdong Shi, Yao Tian, Zhijing Zhang, Sifu Fang, Fan Pan, Lin Qiu, Zhen Bao
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引用次数: 0

摘要

结直肠癌(CRC)患者从传统化疗中获益有限,这突出了改进治疗策略的必要性。天然化合物因其有效的抗癌特性和较少的副作用而成为有希望的替代品。他玛西汀是一种从印楝中提取的o -甲基化黄酮醇,但其抑制结直肠癌进展的潜力和临床应用尚不清楚。为探讨其作用机制,采用体外实验评价他玛西汀对结直肠癌的抑制作用;他马西汀介导的肿瘤抑制在CRC异种移植和患者来源的类器官中进行了验证。我们的研究结果表明,他马西汀以剂量依赖的方式显著降低CRC细胞(HT-29和HCT-116)的增殖,对正常结肠上皮细胞的影响最小(NCM460)。此外,他玛西汀抑制CRC细胞的增殖、迁移和侵袭,导致异种移植肿瘤生长减少,并使CRC对奥沙利铂敏感。机制上,他玛西汀抑制CRC细胞中DPP7的表达和蛋白水平,导致WNT3A/β-catenin信号通路下调。本研究强调,他玛西汀通过干扰dpp7介导的WNT3A/β-catenin信号通路,是一种很有前景的CRC治疗天然化合物。这些发现为改善结直肠癌的预后提供了一种新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tamarixetin Suppresses Colorectal Cancer Progression by Targeting DPP7-Mediated WNT3A/β-Catenin Signalling Pathway

Tamarixetin Suppresses Colorectal Cancer Progression by Targeting DPP7-Mediated WNT3A/β-Catenin Signalling Pathway

Colorectal cancer (CRC) patients have had limited benefits from conventional chemotherapy, highlighting the need for improved therapeutic strategies. Natural compounds have emerged as promising alternatives due to their potent anti-cancer properties and reduced side effects. Tamarixetin is an O-methylated flavonol derived from Azadirachta indica, but its potential and clinical utility to suppress CRC progression remain unknown. To figure out the underlying mechanism, the inhibitory effects of Tamarixetin on CRC were evaluated by in vitro assays; the validation of Tamarixetin-mediated tumour suppression was performed with CRC xenografts and patient-derived organoids. Our results demonstrated that Tamarixetin significantly reduced the proliferation of CRC cells (HT-29 and HCT-116) in a dose-dependent manner, with minimal effects on normal colonic epithelial cells (NCM460). Furthermore, Tamarixetin inhibited proliferation, migration, and invasion of CRC cells, leading to reduced xenograft tumour growth and sensitising CRC to Oxaliplatin. Mechanistically, The expression and protein levels of DPP7 in CRC cells were suppressed by Tamarixetin, which lead to the downregulation of WNT3A/β-catenin signalling pathway. This study highlights Tamarixetin as a promising natural compound for CRC treatment by interfering with DPP7-mediated WNT3A/β-catenin signalling pathway. These findings provide a novel therapeutic strategy to improve outcomes of CRC.

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来源期刊
CiteScore
11.50
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0.00%
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期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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