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Astaxanthin as an Anticancer Agent against Breast Cancer: An In Vivo and In Vitro Investigation.
Shokrian Zeini, Maryam; Pakravesh, Seyyed Mohammad; Jalili Kolour, Seyed Mostafa; Soghala, Shahrad; Dabbagh Ohadi, Mohammad Amin; Ghanbar Ali Akhavan, Haniyeh; Sayyahi, Zeinab; Mahya, Lena; Jahani, Saleheh; Shojaei Baghini, Sadegh; Farkhondeh, Tahereh; Kabiri, Mahboubeh; Samarghandian, Saeed.
Afiliación
  • Shokrian Zeini M; Department of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND, United States.
  • Pakravesh SM; Department of Biotechnology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
  • Jalili Kolour SM; Cellular and Molecular Biology master student, Department of Life Sciences and Systems Biology, University of Turin, Italy.
  • Soghala S; Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran.
  • Dabbagh Ohadi MA; Students'Scientific Research Center, Tehran University of Medical Sciences, Tehran, Iran.
  • Ghanbar Ali Akhavan H; School of Medicine, Arak University of Medical Sciences, Arak, Iran.
  • Sayyahi Z; Department of Physiology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
  • Mahya L; Coenzyme R Research Institute, Tehran, Iran.
  • Jahani S; Coenzyme R Research Institute, Tehran, Iran.
  • Shojaei Baghini S; Plant Biotechnology Department, National Institute of Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran.
  • Farkhondeh T; Department of Toxicology and Pharmacology, School of Pharmacy, Birjand University of Medical Sciences, Birjand, Iran.
  • Kabiri M; Department of Biotechnology, College of Science, University of Tehran, Tehran, Iran.
  • Samarghandian S; Healthy Ageing Research Centre, Neyshabur University of Medical Sciences, Neyshabur, Iran.
Curr Med Chem ; 2024 Apr 17.
Article en En | MEDLINE | ID: mdl-38638038
ABSTRACT

AIM:

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:

ASX could inhibit some tumor progression by using in vivo and in vitro models.

OBJECTIVE:

The effect of ASX on breast cancer was not fully understood till now.

METHOD:

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:

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:

ASX can be considered a promising alternative treatment for breast cancer.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Curr Med Chem Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Curr Med Chem Asunto de la revista: QUIMICA Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos
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