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铱基配合物抗肺癌的研究现状

Current status of iridium-based complexes against lung cancer.

作者信息

Yang Tongfu, Zhu Minghui, Jiang Ming, Yang Feng, Zhang Zhenlei

机构信息

State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources/Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), Collaborative Innovation Center for Guangxi Ethnic Medicine, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin, Guangxi, China.

School of food and biochemical engineering, Guangxi Science and Technology Normal University, Laibin, Guangxi, China.

出版信息

Front Pharmacol. 2022 Sep 23;13:1025544. doi: 10.3389/fphar.2022.1025544. eCollection 2022.

Abstract

Lung cancer is one of the most common malignant tumors, with the highest mortality rate in the world, and its incidence is second only to breast cancer. It has posed a serious threat to human health. Cisplatin, a metal-based drug, is one of the most widely used chemotherapeutic agents for the treatment of various cancers. However, its clinical efficacy is seriously limited by numerous side effects and drug resistance. This has led to the exploration and development of other transition metal complexes for the treatment of malignant tumors. In recent years, iridium-based complexes have attracted extensive attention due to their potent anticancer activities, limited side effects, unique antitumor mechanisms, and rich optical properties, and are expected to be potential antitumor drugs. In this review, we summarize the recent progress of iridium complexes against lung cancer and introduce their anti-tumor mechanisms, including apoptosis, cycle arrest, inhibition of lung cancer cell migration, induction of immunogenic cell death, etc.

摘要

肺癌是最常见的恶性肿瘤之一,是全球死亡率最高的癌症,其发病率仅次于乳腺癌。它对人类健康构成了严重威胁。顺铂作为一种金属基药物,是治疗各种癌症最广泛使用的化疗药物之一。然而,其临床疗效受到众多副作用和耐药性的严重限制。这促使人们探索和开发其他用于治疗恶性肿瘤的过渡金属配合物。近年来,铱基配合物因其强大的抗癌活性、有限的副作用、独特的抗肿瘤机制和丰富的光学性质而受到广泛关注,有望成为潜在的抗肿瘤药物。在本综述中,我们总结了铱配合物抗肺癌的最新进展,并介绍了它们的抗肿瘤机制,包括细胞凋亡、周期阻滞、抑制肺癌细胞迁移、诱导免疫原性细胞死亡等。

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