Anti-tumor effects of Thymus Caramanicus Jalas extract in mice through oxidative stress, inflammation and apoptosis

Author:

Hassanshahi Jalal12,Hajializadeh Zahra3,Niknia Seddigheh4,Mahmoodi Mehdi56,Kaeidi Ayat12ORCID

Affiliation:

1. Physiology-Pharmacology Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences , Rafsanjan , Iran

2. Department of Physiology and Pharmacology, School of Medicine, Rafsanjan University of Medical Sciences , Rafsanjan , Iran

3. Physiology Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences , Kerman , Iran

4. Department of Biochemistry, School of Medicine, Fasa University of Medical Sciences , Fasa , Iran

5. Department of Clinical Biochemistry, Afzalipoor Faculty of Medicine, Kerman University of Medical Sciences , Kerman , Iran

6. Molecular Medicine Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences , Rafsanjan , Iran

Abstract

Abstract Objective Breast cancer causes death in women. Thymus Caramanicus Jalas (TCJ) as a polyphenolic plant has an antiproliferative effect. Accordingly, this investigation studied the TCJ extract anti-tumor effects in a breast cancer model. Methods Twenty-four female BALB/c mice were used in 4 groups including (1) breast cancer (control); (2), (3) and (4) breast cancer + 100, 300 and 500 mg/kg of TCJ extract (once daily for 20-days after breast tumor induction). The breast tumour was induced by 4T1 cell carcinoma injection. Then tumor size and weight were measured. Tumor necrosis factor-α (TNF-α), nuclear factor κ-B (NF-κB), interleukin-6 (IL-6) as inflammatory markers and also Bcl-2, Bax, cytosolic cytochrome-c, apoptosis-inducing factor, and cleaved caspase-3 as biochemical apoptosis markers were evaluated in tumor tissue with western blotting analysis. Also, malondialdehyde (MDA) concentration, hydrogen peroxidase (H2O2), catalase, glutathione peroxidase (GPx) and superoxide dismutase (SOD) activities were exanimated. Key findings Treatment with TCJ extract (500 mg/kg) decreased the tumor volume, tumor weight, GPx, SOD, and catalase enzyme activity versus the control group (P < 0.05). Also, TCJ (500 mg/kg) extract increased MDA, H2O2, inflammatory and apoptosis markers versus control (P < 0.05). Conclusions Current study showed that TCJ can induce anti-tumour effects via promoting inflammation, apoptosis, and oxidative stress in breast tumour tissue.

Funder

Rafsanjan University of Medical Sciences

Publisher

Oxford University Press (OUP)

Subject

Pharmaceutical Science,Pharmacology

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