Half-Sandwich Ru(II) Complexes Bearing 2-(2-quinoly)benzimidazoles with Anticancer Activity

In this article, cytotoxic and apoptotic properties of previously synthesized and characterized four different half‐sandwich ruthenium (II) complexes (C1-C4) with 2-(2-quinoly) benzimidazole frameworks (L1-L5) were described. These Ru (II) complexes (C1-C4) had strong cytotoxic activity towards the human glioblastoma (U373) cancer cell line with low toxicity to the non-cancerous human embryonic kidney (HEK293) cell line. Mechanistic studies revealed that all complexes caused apoptosis induction by activating caspases with upregulation of Bax and downregulation of Bcl-2. Our results indicate that ruthenium (II) complexes with 2-(2-quinoly) benzimidazole frameworks, especially C1 and C4, had a higher cytotoxic and apoptotic activity in human glioblastoma cells, and they should be further evaluated in detail for its anticancer properties as a new therapeutical strategy for glioblastoma.

Publication Details

Journal
Biointerface Research in Applied Chemistry
Published
2024-08-15
DOI
https://doi.org/10.33263//briac144.082
Primary Topic
Metal complexes synthesis and properties
Type
article
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article

Half-Sandwich Ru(II) Complexes Bearing 2-(2-quinoly)benzimidazoles with Anticancer Activity

Biointerface Research in Applied Chemistry
Metal complexes synthesis and properties
article

Half-Sandwich Ru(II) Complexes Bearing 2-(2-quinoly)benzimidazoles with Anticancer Activity

article en

Abstract

In this article, cytotoxic and apoptotic properties of previously synthesized and characterized four different half‐sandwich ruthenium (II) complexes (C1-C4) with 2-(2-quinoly) benzimidazole frameworks (L1-L5) were described. These Ru (II) complexes (C1-C4) had strong cytotoxic activity towards the human glioblastoma (U373) cancer cell line with low toxicity to the non-cancerous human embryonic kidney (HEK293) cell line. Mechanistic studies revealed that all complexes caused apoptosis induction by activating caspases with upregulation of Bax and downregulation of Bcl-2. Our results indicate that ruthenium (II) complexes with 2-(2-quinoly) benzimidazole frameworks, especially C1 and C4, had a higher cytotoxic and apoptotic activity in human glioblastoma cells, and they should be further evaluated in detail for its anticancer properties as a new therapeutical strategy for glioblastoma.

Biointerface Research in Applied ChemistryVol. 14(4)
Good health and well-being
Openalex Percentile: Top 58%
Metal complexes synthesis and properties
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Half-Sandwich Ru(II) Complexes Bearing 2-(2-quinoly)benzimidazoles with Anticancer Activity · Biointerface Research in Applied Chemistry (2024) | TGRS Research Map | TGRS