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Therapeutic efficiency of Tamoxifen/Orlistat nanocrystals against solid ehrlich carcinoma via targeting TXNIP/HIF1-α/MMP-9/P27 and BAX/Bcl2/P53 signaling pathways.
- Source :
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Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2024 Nov; Vol. 180, pp. 117429. Date of Electronic Publication: 2024 Sep 17. - Publication Year :
- 2024
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Abstract
- Background: Orlistat (Orli) is an anti-obesity medication that has been approved by the US Food and Drug Administration. It has relatively limited oral bioavailability with promising inhibitory effects on cell proliferation as well as reducing the growth of tumors.<br />Aims: This investigation was done to evaluate the potential protective effect of Tamoxifen/Orlistat nanocrystals alone or in combination against Solid Ehrlich Carcinoma (SEC) and to clarify the possible underlying influences.<br />Materials and Methods: The liquid antisolvent precipitation technique (bottom-up technology) was utilized to manufacture Orlistat Nanocrystals. To explore potential causes for the anti-tumor action, female Swiss Albino mice bearing SEC were randomly assigned into five equal groups (n = 6). Group 1: Tumor control group, group 2: Tam group: tamoxifen (0.01 g/kg, IP), group 3: Free-Orli group: orlistat (0.24 g/kg, IP), group 4: Nano-Orli: orlistat nanocrystals (0.24 g/kg, IP), group 5: Tam-Nano-Orli: Both doses of Tam and Nano-Orli. All treatments were administered for 16 days.<br />Key Findings: The untreated mice showed development in the tumor volume and weight. As well as histopathology results from these mice revealed many tumor large cells as well as solid sheets of malignant cells. Also, untreated mice showed raised VEGF and TGF-1beta content. Moreover, results of gene expression in the SEC-bearing mice noted upregulation in HIF-1α, MMP-9, Bcl-2, and P27 gene expression and downregulation of TXNIP, BAX, and P53 gene expression. On the other hand, administrated TAM, Free-Orli, Nano-Orli, and a combination of Tam-Nano-Orli distinctly suppressed the tumor effects on estimated parameters with special reference to Tam-Nano-Orli.<br />Significance: The developed Tamoxifen/Orlistat nanocrystals combination could be considered a promising approach to augment antitumor effects.<br />Competing Interests: Declaration of Competing Interest The authors declare that there is no conflict of interest.<br /> (Copyright © 2024. Published by Elsevier Masson SAS.)
- Subjects :
- Animals
Female
Mice
bcl-2-Associated X Protein metabolism
bcl-2-Associated X Protein genetics
Carrier Proteins metabolism
Carcinoma, Ehrlich Tumor drug therapy
Carcinoma, Ehrlich Tumor pathology
Nanoparticles chemistry
Hypoxia-Inducible Factor 1, alpha Subunit metabolism
Matrix Metalloproteinase 9 metabolism
Matrix Metalloproteinase 9 genetics
Signal Transduction drug effects
Tamoxifen pharmacology
Tumor Suppressor Protein p53 metabolism
Tumor Suppressor Protein p53 genetics
Proto-Oncogene Proteins c-bcl-2 metabolism
Proto-Oncogene Proteins c-bcl-2 genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 180
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 39293373
- Full Text :
- https://doi.org/10.1016/j.biopha.2024.117429