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Two multifunctional zero-dimensional Gd(III) complexes: magnetocaloric effect and anticancer mechanisms for lung
Shouying Cao1, Yaqing Xie1, Xiaotong Lu1
1Department of Pharmaceutical Engineering, Anhui Provincial Key Laboratory of Tumor Evolution and Intelligent Diagnosis and Treatment, Bengbu Medical University, Bengbu 233030, PR China.
Two novel gadolinium(III) complexes, Gd1 and Gd2, synthesized using a Schiff base ligand, show significant potential as anticancer agents. They effectively inhibit tumor cell proliferation, migration, and induce apoptosis in A549 cells, outperforming cisplatin.
Area of Science:
- Inorganic Chemistry
- Materials Science
- Biomedical Applications
Background:
- Schiff base ligands are versatile building blocks for metal complexes.
- Gadolinium(III) complexes are explored for their magnetic and therapeutic properties.
- Developing new anticancer agents with improved efficacy and reduced side effects is crucial.
Purpose of the Study:
- To synthesize and characterize novel gadolinium(III) complexes (Gd1 and Gd2) using a Schiff base ligand.
- To investigate the magnetic properties and potential magnetocaloric effects of the synthesized complexes.
- To evaluate the antiproliferative, apoptosis-inducing, and anti-migration activities of Gd1 and Gd2 against tumor cell lines.
Main Methods:
- Synthesis and crystallographic analysis of Gd(III) complexes.
- Magnetic susceptibility measurements to determine magnetic properties.
- In vitro antiproliferative assays, apoptosis assays, cell migration assays, cell cycle analysis, and Western blotting.
Main Results:
- Gd1 and Gd2 were synthesized and structurally characterized as mononuclear and binuclear complexes, respectively.
- The complexes exhibit potential magnetocaloric effects due to Gd(III) ions.
- Gd1 and Gd2 demonstrated significant antiproliferative activity against A549 cells, surpassing cisplatin.
- Administration of Gd1 and Gd2 induced apoptosis, increased reactive oxygen species (ROS) levels, inhibited cell migration, and caused G0/G1 cell cycle arrest in A549 cells.
- Western blotting confirmed modulation of Bcl-2 and Bax protein expression, promoting apoptosis.
Conclusions:
- The synthesized Gd(III) complexes show promising anticancer properties.
- Gd1 and Gd2 represent potential therapeutic agents for cancer treatment, particularly for A549 lung cancer.
- Further research into their mechanism of action and in vivo efficacy is warranted.
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