Astaxanthin as an Anticancer Agent against Breast Cancer: An

Astaxanthin apoptosis breast cancer cytotoxicity in vitro. in vivo oxidative stress

Journal

Current medicinal chemistry
ISSN: 1875-533X
Titre abrégé: Curr Med Chem
Pays: United Arab Emirates
ID NLM: 9440157

Informations de publication

Date de publication:
17 Apr 2024
Historique:
received: 22 10 2023
revised: 16 02 2024
accepted: 26 02 2024
medline: 19 4 2024
pubmed: 19 4 2024
entrez: 19 4 2024
Statut: aheadofprint

Résumé

This study aimed to investigate the antioxidant properties, cytotoxic activity, and apoptotic effects of astaxanthin (ASX) on genes and pathways involved in breast cancer in Balb/c mice models injected with the 4T1 cell line. ASX could inhibit some tumor progression by using in vivo and in vitro models. The effect of ASX on breast cancer was not fully understood till now. In an in vivo model, 4T1 cells-injected mice were administered with different concentrations of ASX (100 and 200 mg/kg), and histopathological evaluations were done using an optical microscope and the hematoxylin and eosin (H&E) staining. The real- time PCR investigated the expression levels of B-cell lymphoma 2-associated X (Bax), B-cell lymphoma 2 (Bcl-2), and Caspase 3 genes in mice treated with 100 and 200 mg/kg ASX. Also, the level of superoxide dismutase (SOD) and malondialdehyde (MDA) were examined in ASX-treated cancer mice. ASX (200 mg/kg) caused a significant reduction in the mitotic cell count of tumor tissues compared to ASX (100 mg/kg). The antiproliferative effects of different concentrations of ASX were shown based on the MTT results. The treatment of breast tumor mice with both concentrations of ASX, especially 200 mg/kg, elevated the expression of Caspase 3, Bax, and SOD enzyme levels and decreased Bcl-2 expression and MDA enzyme levels. ASX can be considered a promising alternative treatment for breast cancer.

Sections du résumé

AIM OBJECTIVE
This study aimed to investigate the antioxidant properties, cytotoxic activity, and apoptotic effects of astaxanthin (ASX) on genes and pathways involved in breast cancer in Balb/c mice models injected with the 4T1 cell line.
BACKGROUND BACKGROUND
ASX could inhibit some tumor progression by using in vivo and in vitro models.
OBJECTIVE OBJECTIVE
The effect of ASX on breast cancer was not fully understood till now.
METHOD METHODS
In an in vivo model, 4T1 cells-injected mice were administered with different concentrations of ASX (100 and 200 mg/kg), and histopathological evaluations were done using an optical microscope and the hematoxylin and eosin (H&E) staining. The real- time PCR investigated the expression levels of B-cell lymphoma 2-associated X (Bax), B-cell lymphoma 2 (Bcl-2), and Caspase 3 genes in mice treated with 100 and 200 mg/kg ASX. Also, the level of superoxide dismutase (SOD) and malondialdehyde (MDA) were examined in ASX-treated cancer mice.
RESULTS RESULTS
ASX (200 mg/kg) caused a significant reduction in the mitotic cell count of tumor tissues compared to ASX (100 mg/kg). The antiproliferative effects of different concentrations of ASX were shown based on the MTT results. The treatment of breast tumor mice with both concentrations of ASX, especially 200 mg/kg, elevated the expression of Caspase 3, Bax, and SOD enzyme levels and decreased Bcl-2 expression and MDA enzyme levels.
CONCLUSION CONCLUSIONS
ASX can be considered a promising alternative treatment for breast cancer.

Identifiants

pubmed: 38638038
pii: CMC-EPUB-139810
doi: 10.2174/0109298673288774240406053607
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Maryam Shokrian Zeini (M)

Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND, United States.

Seyyed Mohammad Pakravesh (SM)

Department of Biotechnology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Seyed Mostafa Jalili Kolour (SM)

Cellular and Molecular Biology master student, Department of Life Sciences and Systems Biology, University of Turin, Italy.

Shahrad Soghala (S)

Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.

Mohammad Amin Dabbagh Ohadi (MA)

Students'Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran.

Haniyeh Ghanbar Ali Akhavan (H)

School of Medicine, Arak University of Medical Sciences, Arak, Iran.

Zeinab Sayyahi (Z)

Department of Physiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

Lena Mahya (L)

Coenzyme R Research Institute, Tehran, Iran.

Saleheh Jahani (S)

Coenzyme R Research Institute, Tehran, Iran.

Sadegh Shojaei Baghini (S)

Plant Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.

Tahereh Farkhondeh (T)

Department of Toxicology and Pharmacology, School of Pharmacy, Birjand University of Medical Sciences, Birjand, Iran.

Mahboubeh Kabiri (M)

Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.

Saeed Samarghandian (S)

Healthy Ageing Research Centre, Neyshabur University of Medical Sciences, Neyshabur, Iran.

Classifications MeSH