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海洋生物活性化合物在癌症信号通路中的潜在作用:综述。

Potential role of Marine Bioactive Compounds in cancer signaling pathways: A review.

机构信息

Molecular Toxicology Laboratory, Department of Biotechnology, Bharathiar University, Coimbatore, 641046, Tamil Nadu, India.

Molecular Toxicology Laboratory, Department of Biotechnology, Bharathiar University, Coimbatore, 641046, Tamil Nadu, India.

出版信息

Eur J Pharmacol. 2022 Dec 5;936:175330. doi: 10.1016/j.ejphar.2022.175330. Epub 2022 Oct 17.

Abstract

Cancer is characterized by alterations that cause the over-proliferation of cells and hyperactivation of signaling pathways. Alterations of signaling molecules dysregulate physiological functions like cell growth, proliferation, metastasis, and cell death. Hence, the potential anticancer compounds primarily target signaling networks for therapeutic interventions in cancer. In the past few years, cancer therapy directed its focus on bioactive compounds that originated from marine sources considering their diverse and untapped nature. These Marine Bioactive Compounds (MBCs) are broadly classified into distinct categories such as alkaloids, carbohydrates, fatty acids, peptides, phenols, quinones, terpenes, and saponins. Bioactive compounds from each class initiate cell death via different signaling pathways. The primary objective of this review is to provide comprehensive information about the pathways that are predominantly targeted by every class of MBCs and integrating data from several marine anticancer research. Here, we studied the role of MBCs in signaling networks that inhibit various cancer types. As a result, we concluded that PI3K/AKT, ROS, and p53 are the three prime signaling pathways targeted by the MBCs to induce apoptosis in cancer cells. Carbohydrates, peptides, and terpenes are the major MBCs classes that regulate signaling pathways in cancer. Hence it is concluded that future anticancer research can be primarily focused on the MBCs derived from the scrutinized classes that adhere to pathways like PI3K/AKT, ROS, and p53 to achieve par excellence results.

摘要

癌症的特征是导致细胞过度增殖和信号通路过度激活的改变。信号分子的改变会使细胞生长、增殖、转移和细胞死亡等生理功能失调。因此,潜在的抗癌化合物主要针对信号网络,作为癌症治疗的干预靶点。在过去的几年中,癌症治疗将其重点放在了源自海洋来源的生物活性化合物上,因为它们具有多样性和未开发的特性。这些海洋生物活性化合物(MBCs)广泛分为不同的类别,如生物碱、碳水化合物、脂肪酸、肽、酚类、醌类、萜类和皂苷。每一类生物活性化合物都通过不同的信号通路引发细胞死亡。本综述的主要目的是提供关于每一类 MBCs 主要靶向的途径的综合信息,并整合来自多个海洋抗癌研究的数据。在这里,我们研究了 MBCs 在抑制各种癌症类型的信号网络中的作用。结果表明,PI3K/AKT、ROS 和 p53 是 MBCs 诱导癌细胞凋亡的三个主要信号通路。碳水化合物、肽和萜类是调节癌症中信号通路的主要 MBC 类。因此,可以得出结论,未来的抗癌研究可以主要集中在从经过仔细筛选的类别的 MBCs 中获得,这些 MBCs 遵循 PI3K/AKT、ROS 和 p53 等途径,以取得卓越的效果。

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