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An organotin indomethacin derivative inhibits cancer cell proliferation and synergizes the antiproliferative effects of lapatinib in breast cancer cells

机译:有机汀吲哚美辛衍生物抑制癌细胞增殖并协同rapatinib在乳腺癌细胞中的抗增殖作用

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摘要

It is known that an inflammatory condition in different types of cancer provides a sustained microenvironment that favors tumor growth, invasion, and metastasis. Non-steroidal anti-inflammatory drugs such as indomethacin have demonstrated chemo-preventive, anti-proliferative and cytotoxic effects in a variety of tumors. The aim of this study was to investigate the effects of an organotin indomethacin derivative (OID) on the proliferation of breast and prostate cancer cell lines and the possible mechanisms of action of this compound. Different cancer cell lines were treated in the presence of OID and cell proliferation was measured by quantification of the DNA content, changes in the cell cycle profile and the activation of caspase 3 were evaluated by flow cytometry, interleukin 6 (IL-6) gene expression was evaluated by qPCR and protein expression was analyzed by ELISA and Western blot assays. OID inhibited the cell proliferation of a panel of cancer cell lines in a concentration-dependent manner. Moreover, the addition of OID to lapatinib treatment, targeted therapy for breast cancer, significantly enhanced its antiproliferative response. The effects on cell proliferation of these compounds involved, among others, the induction of apoptosis, the downregulation of IL-6 and a decrease of the MAPK activation pathway. Our results suggest that the use of OID alone or in combination with tyrosine kinase inhibitors could be considered as adjuvants in the treatment of cancer.
机译:众所周知,不同类型癌症中的炎症病症提供了持续的微环境,可伴随肿瘤生长,侵袭和转移。非甾体抗炎药,如吲哚美辛,在各种肿瘤中表现出化学预防,抗增殖和细胞毒性作用。本研究的目的是探讨有机素吲哚美辛衍生物(OID)对乳腺癌和前列腺癌细胞系的增殖以及该化合物的可能作用机制的影响。在oid的存在下处理不同的癌细胞系,通过定量DNA含量测量细胞增殖,通过流式细胞术,白细胞介素6(IL-6)基因表达评估细胞周期曲线的变化和胱天蛋白3的活化通过QPCR和蛋白质表达通过ELISA和Western印迹测定评估。 OID以浓度依赖性方式抑制癌细胞系的细胞增殖。此外,对Lapatinib治疗的oid oid靶向治疗乳腺癌,显着增强了其抗增殖反应。对涉及这些化合物的细胞增殖的影响,其中诱导细胞凋亡,IL-6的下调和MAPK活化途径的降低。我们的研究结果表明,单独使用OID或与酪氨酸激酶抑制剂的使用可以被认为是治疗癌症的佐剂。

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