4.7 Review

Ruthenium Complexes: An Alternative to Platinum Drugs in Colorectal Cancer Treatment

期刊

PHARMACEUTICS
卷 13, 期 8, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics13081295

关键词

ruthenium; nanoparticles; colorectal cancer; treatment; diagnosis

资金

  1. Research Creativity and Management (RCMO), Universiti Sains Malaysia (USM)
  2. School of Medical Sciences, USM

向作者/读者索取更多资源

Ru-based compounds exhibit promising anticancer activity in CRC cells and may serve as alternatives to Pt-based anticancer drugs. Ru nanoparticles coupled with photosensitizers or anticancer agents have therapeutic and diagnostic potential for CRC. Clinical trials of Ru (III)-based drug NKP-1339 have been conducted in CRC treatment.
Colorectal cancer (CRC) is one of the intimidating causes of death around the world. CRC originated from mutations of tumor suppressor genes, proto-oncogenes and DNA repair genes. Though platinum (Pt)-based anticancer drugs have been widely used in the treatment of cancer, their toxicity and CRC cells' resistance to Pt drugs has piqued interest in the search for alternative metal-based drugs. Ruthenium (Ru)-based compounds displayed promising anticancer activity due to their unique chemical properties. Ru-complexes are reported to exert their anticancer activities in CRC cells by regulating different cell signaling pathways that are either directly or indirectly associated with cell growth, division, proliferation, and migration. Additionally, some Ru-based drug candidates showed higher potency compared to commercially available Pt-based anticancer drugs in CRC cell line models. Meanwhile Ru nanoparticles coupled with photosensitizers or anticancer agents have also shown theranostic potential towards CRC. Ru-nanoformulations improve drug efficacy, targeted drug delivery, immune activation, and biocompatibility, and therefore may be capable of overcoming some of the existing chemotherapeutic limitations. Among the potential Ru-based compounds, only Ru (III)-based drug NKP-1339 has undergone phase-Ib clinical trials in CRC treatment.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据