Organogallium(III) complexes as apoptosis promoting anticancer agents for head and neck squamous cell carcinoma (HNSCC) cell lines

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• 作者：Milena R. Kaluđ ; erović ; ^a ; Goran N. Kaluđ ; erović ; ^b ; ^c ; ^{goran.kaluderovic@chemie.uni-halle.de} ; Santiago Gó ; mez-Ruiz^d ; Reinhard Paschke^b ; Alexander Hemprich^a ; Jan Kü ; hling^e ; Torsten W. Remmerbach^a ; ^f
• 关键词：Anticancer drugs ; Cytotoxicity ; Apoptosis ; Caspase activity ; Cell cycle ; Gallium(III) complexes
• 刊名：Journal of Inorganic Biochemistry
• 出版年：2011
• 出版时间：February 2011
• 年：2011
• 卷：105
• 期：2
• 页码：164-170
• 全文大小：452 K

文摘

Organogallium(III) dinuclear (1–9) and tetranuclear (10) complexes present potential therapeutic agents for the treatment of various types of cancer. The antiproliferative activity of 1–10 was evaluated with cell lines of head and neck squamous cell carcinomas, e.g. HN (soft palate), Cal27, Cal33 (tongue) and FaDu (hypopharynx) cell lines. The activity of compound 8 is comparable with that of cisplatin on cell line Cal27 (IC₅₀ 4.6 μM for both compounds). The mode of cell death induced, caspase activity and cell cycle analysis were evaluated for potential hit compounds 3, 5 and 8 Potential hit compounds 3, 5 and 8 were further evaluated for the mode of cell death, caspase activity and cell cycle analysis. Apoptosis induced by compounds 3, 5 and 8 on Cal27 and FaDu cells was confirmed by DNA laddering , as well as acridine orange (AO) and ethidium bromide (EB) double staining. These compounds (3, 5 and 8) induced caspase-independent apoptosis (within 4 h of action) in cell line Cal27. Extrinsic-mediated apoptosis associated with caspase 8 and 3 activation is the main mode of cytotoxicity induced on FaDu cells by compounds 3, 5 and 8. Cell cycle perturbations caused by these compounds are also observed. Our data suggest that compounds 3, 5 and 8 should be studied further for the treatment of head and neck cancer.