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诺多辛通过抑制增殖和引发复杂的细胞死亡发挥抗结直肠癌作用。

Nodosin Exerts an Anti-Colorectal Cancer Effect by Inhibiting Proliferation and Triggering Complex Cell Death and .

作者信息

Fan Huixia, Hao Xiaopeng, Gao Yuan, Yang Jian, Liu Aojun, Su Yarui, Xia Yong

机构信息

School of Life Sciences, Henan University, Kaifeng, China.

Key Laboratory of Precision Oncology of Shandong Higher Education, Institute of Precision Medicine, Jining Medical University, Jining, China.

出版信息

Front Pharmacol. 2022 Jul 22;13:943272. doi: 10.3389/fphar.2022.943272. eCollection 2022.

Abstract

Colorectal cancer (CRC) is one of the most common digestive system cancer in the world. Its incidence and mortality are increasing annually. Presently, CRC lacks long-term effective treatment methods and drugs. Therefore, finding new treatment methods and drugs is of great significance for CRC treatment. Compounds derived from natural plants have been widely used in tumor research and treatment because of their good antitumor activity these years. This study found that nodosin, a diterpenoid extracted from the medicinal plant inhibited the growth of CRC cells SW480, HT-29 and LoVo in a dose- and time-dependent manner, with inhibitory concentrations (IC) of 7.4, 7.7, and 6.6 μM respectively. We selected highly metastatic and poorly differentiated SW480 cells for further studies. We found that nodosin could inhibit cell proliferation by inhibiting DNA synthesis and induce cell death by inducing oxidative stress, apoptosis and autophagy in cells. Through assays combined with transcriptomic analysis, it was found that nodosin could downregulate tribbles pseudokinase 3 and upregulate oxidative stress-induced growth inhibitor 1 to induce oxidative stress in cells; nodosin-induced reactive oxygen species were able to upregulate the expression of heme oxygenase 1 to induce apoptosis and the expression of cathepsin L. and light chain-3 to induce autophagy. , we found that nodosin inhibited tumor growth and induced cells to undergo apoptosis and autophagy without significant toxic effects. In conclusion, our findings suggest that nodosin exerts anti-CRC effects mainly through its ability to induce apoptosis and autophagy and . Therefore, our study contributes to the development of nodosin-based potential CRC therapeutic drugs.

摘要

结直肠癌(CRC)是世界上最常见的消化系统癌症之一。其发病率和死亡率逐年上升。目前,CRC缺乏长期有效的治疗方法和药物。因此,寻找新的治疗方法和药物对CRC治疗具有重要意义。近年来,天然植物来源的化合物因其良好的抗肿瘤活性而被广泛应用于肿瘤研究和治疗。本研究发现,从药用植物中提取的二萜类化合物诺多辛以剂量和时间依赖性方式抑制CRC细胞SW480、HT - 29和LoVo的生长,抑制浓度(IC)分别为7.4、7.7和6.6μM。我们选择高转移性和低分化的SW480细胞进行进一步研究。我们发现诺多辛可通过抑制DNA合成来抑制细胞增殖,并通过诱导细胞内氧化应激、凋亡和自噬来诱导细胞死亡。通过实验结合转录组分析发现,诺多辛可下调 Tribbles 假激酶3并上调氧化应激诱导生长抑制剂1以诱导细胞内氧化应激;诺多辛诱导的活性氧能够上调血红素加氧酶1的表达以诱导凋亡以及组织蛋白酶L和轻链3的表达以诱导自噬。我们发现诺多辛抑制肿瘤生长并诱导细胞发生凋亡和自噬,且无明显毒性作用。总之,我们的研究结果表明,诺多辛主要通过其诱导凋亡和自噬的能力发挥抗CRC作用。因此,我们的研究有助于开发基于诺多辛的潜在CRC治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/caa5/9353177/edf2e4815b19/fphar-13-943272-g001.jpg

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