Improving Tamoxifen Performance in Inducing Apoptosis and Hepatoprotection by Loading on a Dual Nanomagnetic Targeting System
- Authors: Zhao Y.1, Ding W.2, Zhang P.2, Deng L.2, Long Y.2, Lu J.2, Shiri F.3, Heidari Majd M.4
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Affiliations:
- Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology, YanAn Hospital Affiliated To Kunming Medical University
- Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
- Department of Chemistry, University of Zabol
- Department of Medicinal Chemistry, Faculty of Pharmacy, Zabol University of Medical Sciences
- Issue: Vol 24, No 13 (2024)
- Pages: 1016-1028
- Section: Oncology
- URL: https://rjsocmed.com/1871-5206/article/view/643822
- DOI: https://doi.org/10.2174/0118715206289666240423091244
- ID: 643822
Cite item
Full Text
Abstract
Background:Although tamoxifen (TMX) belongs to selective estrogen receptor modulators (SERMs) and selectively binds to estrogen receptors, it affects other estrogen-producing tissues due to passive diffusion and non-differentiation of normal and cancerous cells and leads to side effects.
Methods:The problems expressed about tamoxifen (TMX) encouraged us to design a new drug delivery system based on magnetic nanoparticles (MNPs) to simultaneously target two receptors on cancer cells through folic acid (FA) and hyaluronic acid (HA) groups. The mediator of binding of two targeting agents to MNPs is a polymer linker, including dopamine, polyethylene glycol, and terminal amine (DPN).
Results:Zeta potential, dynamic light scattering (DLS), and Field emission scanning electron microscopy (FESEM) methods confirmed that MNPs-DPN-HA-FA has a suitable size of ~105 nm and a surface charge of -41 mV, and therefore, it can be a suitable option for carrying TMX and increasing its solubility. The cytotoxic test showed that the highest concentration of MNPs-DPN-HA-FA-TMX decreased cell viability to about 11% after 72 h of exposure compared to the control. While the protective effect of modified MNPs on normal cells was evident, unlike tamoxifen, the survival rate of liver cells, even after 180 min of treatment, was not significantly different from the control group. The protective effect of MNPs was also confirmed by examining the amount of malondialdehyde, and no significant difference was observed in the amount of lipid peroxidation caused by modified MNPs compared to the control. Flow cytometry proved that TMX loaded onto modified MNPs can induce apoptosis by targeting the overexpressed receptors on cancer cells. Real-time PCR showed that the modified MNPs activated the intrinsic and extrinsic mitochondrial pathways of apoptosis, so the Bak1/Bclx ratio for MNPs-DPN-HAFA- TMX and free TMX was 70.82 and 0.38, respectively. Also, the expression of the caspase-3 gene increased 430 times compared to the control. On the other hand, only TNF gene expression, which is responsible for metastasis in some tumors, was decreased by both free TMX and MNPs-DPN-HA-FA-TMX. Finally, molecular docking proved that MNPs-DPN-HA-FA-TMX could provide a very stable interaction with both CD44 and folate receptors, induce apoptosis in cancer cells, and reduce hepatotoxicity.
Conclusion:All the results showed that MNPs-DPN-HA-FA-TMX can show good affinity to cancer cells using targeting agents and induce apoptosis in metastatic breast ductal carcinoma T-47D cell lines. Also, the protective effects of MNPs on hepatocytes are quite evident, and they can reduce the side effects of TMX.
About the authors
Yanfang Zhao
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology, YanAn Hospital Affiliated To Kunming Medical University
Email: info@benthamscience.net
Wanbao Ding
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
Email: info@benthamscience.net
Peixian Zhang
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
Email: info@benthamscience.net
Lei Deng
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
Email: info@benthamscience.net
Yi Long
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
Email: info@benthamscience.net
Jiuqin Lu
Key Laboratory of Tumor Immunological Prevention and Treatment, Department of Oncology,, YanAn Hospital Affiliated To Kunming Medical University
Author for correspondence.
Email: info@benthamscience.net
Fereshteh Shiri
Department of Chemistry, University of Zabol
Email: info@benthamscience.net
Mostafa Heidari Majd
Department of Medicinal Chemistry, Faculty of Pharmacy, Zabol University of Medical Sciences
Email: info@benthamscience.net
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