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紫色墨汁分泌物对人肝癌细胞系(HepG2)的细胞毒性作用:体外和计算机模拟研究。

Purple Ink Secretion Concentrate Exerts Cytotoxic Properties against Human Hepatocarcinoma Cell Line (HepG2): In Vitro and In Silico Studies.

机构信息

King Abdullah International Medical Research Center, King Saud bin Abdulaziz University for Health Sciences, Riyadh 11481, Saudi Arabia.

PG & Research Department of Biochemistry, Mohamed Sathak Arts and Science College, Tamil Nadu 600119, India.

出版信息

Molecules. 2022 Jan 26;27(3):826. doi: 10.3390/molecules27030826.

DOI:10.3390/molecules27030826
PMID:35164089
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8839718/
Abstract

Liver cancer is a leading cause of cancer death globally. Marine mollusc-derived drugs have gained attention as potential natural-based anti-cancer agents to overcome the side effects caused by conventional chemotherapeutic drugs during cancer therapy. Using liquid chromatography-mass spectrometry, the main biomolecules in the purple ink secretion released by the sea hare, named (), were identified as hectochlorin, malyngamide X, malyngolide S, bursatellin and lyngbyatoxin A. The cytotoxic effects of ink concentrate against human hepatocarcinoma (HepG2) cells were determined to be dose- and time-dependent, and further exploration of the underlying mechanisms causing the programmed cell death (apoptosis) were performed. The expression of cleaved-caspase-8 and cleaved-caspase-3, key cysteine-aspartic proteases involved in the initiation and completion of the apoptosis process, appeared after HepG2 cell exposure to the ink concentrate. The gene expression levels of pro-apoptotic , and were increased after treatment with the ink concentrate. Applying in silico approaches, the high scores predicted that bioactivities for the five compounds were protease and kinase inhibitors. The ADME and cytochrome profiles for the compounds were also predicted. Altogether, the ink concentrate has high pro-apoptotic potentials, suggesting it as a promising safe natural product-based drug for the treatment of liver cancer.

摘要

肝癌是全球癌症死亡的主要原因。海洋软体动物衍生的药物作为潜在的天然抗癌药物受到关注,以克服癌症治疗过程中常规化疗药物引起的副作用。利用液相色谱-质谱联用技术,鉴定出海兔紫色墨囊分泌物中的主要生物分子为海兔内酯、马良酰胺 X、马良醇 S、鲍鱼毒素和石房蛤毒素 A。墨囊浓缩物对人肝癌(HepG2)细胞的细胞毒性作用呈剂量和时间依赖性,并进一步探讨了导致程序性细胞死亡(细胞凋亡)的潜在机制。在 HepG2 细胞暴露于墨囊浓缩物后,出现了半胱天冬氨酸蛋白酶家族中参与凋亡过程起始和完成的关键蛋白酶裂解型 caspase-8 和裂解型 caspase-3 的表达。经墨囊浓缩物处理后,促凋亡基因 、 和 的表达水平增加。通过计算方法,高评分表明这 5 种化合物具有蛋白酶和激酶抑制剂的生物活性。还预测了化合物的 ADME 和细胞色素特征。总之,墨囊浓缩物具有较高的促凋亡潜力,表明它是一种有前途的基于天然产物的安全药物,可用于治疗肝癌。

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