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海蜇刺细胞毒液的化学成分及对人腺癌细胞 A549 的实验和计算模拟的抗癌作用。

Chemical Compositions and Experimental and Computational Modeling of the Anticancer Effects of Cnidocyte Venoms of Jellyfish and on Human Adenocarcinoma A549 Cells.

机构信息

Student Research Committee, Bushehr University of Medical Sciences, Bushehr 75, Iran.

PerciaVista R&D Co., Shiraz 73, Iran.

出版信息

Mar Drugs. 2023 Mar 7;21(3):168. doi: 10.3390/md21030168.

Abstract

Nowadays, major attention is being paid to curing different types of cancers and is focused on natural resources, including oceans and marine environments. Jellyfish are marine animals with the ability to utilize their venom in order to both feed and defend. Prior studies have displayed the anticancer capabilities of various jellyfish. Hence, we examined the anticancer features of the venom of and in an in vitro situation against the human pulmonary adenocarcinoma (A549) cancer cell line. The MTT assay demonstrated that both mentioned venoms have anti-tumoral ability in a dose-dependent manner. Western blot analysis proved that both venoms can increase some pro-apoptotic factors and reduce some anti-apoptotic molecules that lead to the inducing of apoptosis in A549 cells. GC/MS analysis demonstrated some compounds with biological effects, including anti-inflammatory, antioxidant and anti-cancer activities. Molecular docking and molecular dynamic showed the best position of each biologically active component on the different death receptors, which are involved in the process of apoptosis in A549 cells. Ultimately, this study has proven that both venoms of and have the capability to suppress A549 cells in an in vitro condition and they might be utilized in order to design and develop brand new anticancer agents in the near future.

摘要

如今,人们主要关注治疗各种癌症,并专注于自然资源,包括海洋和海洋环境。水母是具有利用毒液进食和防御能力的海洋动物。先前的研究已经显示出各种水母具有抗癌能力。因此,我们在体外环境下研究了 和 毒液对人肺腺癌细胞系(A549)的抗癌特性。MTT 分析表明,这两种毒液都具有剂量依赖性的抗肿瘤能力。Western blot 分析证明,这两种毒液都可以增加一些促凋亡因子,减少一些抗凋亡分子,从而导致 A549 细胞凋亡。GC/MS 分析表明,一些具有生物活性的化合物,包括抗炎、抗氧化和抗癌活性。分子对接和分子动力学显示了每个具有生物活性的成分在不同死亡受体上的最佳位置,这些受体参与了 A549 细胞凋亡的过程。最终,这项研究证明了 和 这两种毒液都有能力在体外抑制 A549 细胞,它们可能被用于设计和开发新型抗癌药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/226b/10057638/ed2cc66f2730/marinedrugs-21-00168-g001.jpg

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