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Synthesis characterization and antitumor activity of Ln(III) complexes with hydrazone Schiff base derived from 2-acetylpyridine and isonicotinohydrazone

机译:n-席夫碱衍生自2-乙酰吡啶和异烟肼ino的Ln(III)配合物的合成表征和抗肿瘤活性

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摘要

In the present study, two isostructural lanthanide (Ln)(III) complexes, namely Ln(HL)2(NO3)(CH3OH)2)·CH3OH, where Ln = La in complex 1 and Ce in complex 2, and hydrogen ligand (HL) = (E)-N'-[1-(2-pyridinyl)ethylidene]isonicotinohydrazone, have been isolated and characterized by elemental analysis, infrared spectra and single-crystal X-ray diffraction analysis. The results revealed that the acylhydrazone ligand HL in each complex was deprotonated as an anionic ligand and coordinated to the central La(III) ion via enolization of oxygen and nitrogen atoms. Furthermore, the antitumor effects and potential mechanisms of the two complexes were explored in the human lung cancer cell line A549 and in the human gastric cancer cell lines BGC823 and SGC7901. In the present study, the roles the two complexes on the proliferation and apoptosis of the above tumor cell lines were determined by MTT assay and Annexin V/propidium iodide flow cytometry, respectively. Furthermore, various apoptosis-associated key genes, including caspase 3, B cell lymphoma (Bcl)-2-associated X protein (Bax) and Bcl-2, were detected by western blotting to explore the possible antitumor mechanisms of the two complexes. The results revealed that the two complexes had comparable antitumor activities in terms of inhibiting proliferation and inducing apoptosis in tumor cell lines. The changes in the protein expression levels of caspase 3, Bax and Bcl-2 further verified the apoptosis-promoting mechanisms of the two complexes in tumor cell lines. These findings have a great potential in biomedical applications of novel Ln(III) complexes.
机译:在本研究中,两种同构的镧系元素(Ln)(III)配合物,即Ln(HL)2(NO3)(CH3OH)2)·CH3OH,其中配合物1中的Ln = La和配合物2中的Ce,以及氢配体( HL)=(E)-N'-[1-(2-吡啶基)亚乙基]异烟酰胺hydr已通过元素分析,红外光谱和单晶X射线衍射分析进行了分离和表征。结果表明,每个配合物中的酰基hydr配体HL被去质子化为阴离子配体,并通过烯化氧和氮原子与中心La(III)离子配位。此外,在人肺癌细胞系A549和人胃癌细胞系BGC823和SGC7901中探索了这两种复合物的抗肿瘤作用及其潜在机制。在本研究中,分别通过MTT法和膜联蛋白V /碘化丙啶流式细胞术确定了两种复合物在上述肿瘤细胞系的增殖和凋亡中的作用。此外,通过蛋白质印迹法检测了各种凋亡相关的关键基因,包括胱天蛋白酶3,B细胞淋巴瘤(Bcl)-2-相关的X蛋白(Bax)和Bcl-2,以探索这两种复合物可能的抗肿瘤机制。结果表明,两种复合物在抑制肿瘤细胞系的增殖和诱导细胞凋亡方面具有可比的抗肿瘤活性。 caspase 3,Bax和Bcl-2蛋白表达水平的变化进一步证实了这两种复合物在肿瘤细胞系中的促凋亡机制。这些发现在新型Ln(III)配合物的生物医学应用中具有巨大的潜力。

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