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海藻生物活性化合物的促凋亡作用:开发新型抗癌药物的有前景的来源。

Pro-Apoptotic Activity of Bioactive Compounds from Seaweeds: Promising Sources for Developing Novel Anticancer Drugs.

机构信息

Ingeniería Bioquímica, Escuela Nacional de Ciencias Biológicas (ENCB), Instituto Politécnico Nacional, Mexico City 07738, Mexico.

Consejo Nacional de Ciencia y Tecnología (CONACYT), Universidad Autónoma Metropolitana, Unidad Lerma (UAMLerma), Municipio Lerma de Villada C.P. 52005, Mexico.

出版信息

Mar Drugs. 2023 Mar 15;21(3):182. doi: 10.3390/md21030182.

Abstract

The process by which cancer cells evade or inhibit apoptosis is considered one of the characteristics of cancer. The ability of cancer cells to escape apoptosis contributes to tumor proliferation and promotes metastasis. The discovery of new antitumor agents is essential for cancer treatment due to the lack of selectivity of drugs and cellular resistance to anticancer agents. Several studies showed that macroalgae produce various metabolites with different biological activities among marine organisms. This review discusses multiple metabolites extracted from macroalgae and their pro-apoptotic effects through regulating apoptosis signaling pathway target molecules and the structure-activity relationship. Twenty-four promising bioactive compounds have been reported, where eight of these compounds exhibited values of maximum inhibitory concentration (IC50) of less than 7 μg/mL. Fucoxanthin was the only carotenoid reported that induced apoptosis in HeLa cells with an IC50 below 1 µg/mL. Se-PPC (a complex of proteins and selenylated polysaccharides) is the magistral compound because it is the only one with an IC50 of 2.5 µg/mL which regulates the primary proteins and critical genes of both apoptosis pathways. Therefore, this review will help provide the basis for further studies and the development of new anticancer drugs, both as single agents and adjuvants, decreasing the aggressiveness of first-line drugs and offering patients better survival and quality of life.

摘要

癌细胞逃避或抑制细胞凋亡的过程被认为是癌症的特征之一。癌细胞逃避细胞凋亡的能力有助于肿瘤增殖,并促进转移。由于药物缺乏选择性和细胞对抗癌药物的耐药性,因此发现新的抗肿瘤药物对于癌症治疗至关重要。多项研究表明,海藻在海洋生物中产生各种具有不同生物活性的代谢物。本综述讨论了从海藻中提取的多种代谢物及其通过调节凋亡信号通路靶分子的促凋亡作用,以及它们的结构-活性关系。报告了 24 种有前途的生物活性化合物,其中 8 种化合物的最大抑制浓度(IC50)值低于 7μg/mL。岩藻黄质是唯一一种被报道能以低于 1μg/mL 的 IC50 在 HeLa 细胞中诱导细胞凋亡的类胡萝卜素。Se-PPC(一种蛋白质和硒多糖的复合物)是一种主要化合物,因为它是唯一一种 IC50 为 2.5μg/mL 的化合物,可调节凋亡途径的主要蛋白质和关键基因。因此,本综述将有助于为进一步的研究和开发新的抗肿瘤药物提供基础,无论是作为单一药物还是辅助药物,降低一线药物的侵袭性,为患者提供更好的生存和生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c53/10057668/038cb63f93a0/marinedrugs-21-00182-g001.jpg

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