费鲁拉assafoetida通过JNK/MAPK信号通路激活诱导了结肠癌细胞的分化
Hani M Abdelsalam1,2, Aya M Abdelghany1, Wafaa A Ahmed3
1Department of Zoology, Zagazig University, Zagazig 44519, Egypt.
World journal of experimental medicine
|January 7, 2026
概括
费鲁拉assafoetida通过诱导细胞分化和亡,显示出作为结肠癌治疗的潜力. 这种天然化合物有效地增加细胞死亡,并使结肠癌细胞正常化.
科学领域:
- 在瘤学瘤学.
- 药理学 药理学是指药理学的学科.
- 细胞生物学 细胞生物学
背景情况:
- 结肠癌是一个重大的全球健康挑战,死亡率不断上升.
- 对结肠癌的新型治疗药物的研究至关重要.
研究的目的:
- 评估Ferula assafoetida (F. assafoetida) 作为结肠癌分化剂的疗效.
- 评估F. assafoetida在结肠癌中恢复正常细胞功能的潜力.
主要方法:
- 用MTT测定测量Caco细胞来测量细胞毒性.
- 分析了细胞周期,细胞亡,抗氧化剂水平 (TA,GSH,MDA) 和性酸酶 (ALP) 活性.
- 量化了c-Jun N-终端激酶 (JNK) 和基因激活蛋白激酶 (MAPK) 的基因表达.
主要成果:
- F. assafoetida显著增加了Caco细胞中的细胞亡和细胞死亡.
- 治疗导致了总抗氧化剂和谷氨水平的增加,并减少了甲.
- 观察到JNK和MAPK表达的显著上调,同时增加了ALP活性.
结论:
- 费鲁拉 (Ferula assafoetida) 显示出作为结肠癌治疗剂的潜力.
- F. assafoetida 作为差异化剂,促进正常细胞功能.
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