| Literature DB >> 26300395 |
Vahid Khori1, Sadegh Amani Shalamzari2, Amin Isanejad3, Ali Mohammad Alizadeh4, Shaban Alizadeh5, Saeed Khodayari2, Hamid Khodayari6, Shirin Shahbazi7, Ali Zahedi2, Hamid Sohanaki8, Mahmood Khaniki9, Reza Mahdian10, Mojtaba Saffari11, Raja Fayad12.
Abstract
Exercise training has an anti-tumor effect and can reduce tumor growth; however, the exact underlying mechanisms of its protective effects are still obscure. MicroRNA (miR)-21 is a predictor in cancer survival, and has a potential use as an indicator of therapeutic outcome in breast malignancies. Forty-eight female BALB/c mice were equally divided into six groups to investigate the effects of interval exercise training with tamoxifen on miR-21 expression and its possible assumed mechanisms in an estrogen receptor-positive breast cancer model. ELISA, immunohistochemistry, western blot, qRT-PCR assays were performed at the end of the study. Tumor size was significantly declined in exercise training and tamoxifen groups compared to tumor group (P<0.05). Expression of miR-21 was significantly down-regulated in trained and tamoxifen treated mice in comparison with tumor group (P<0.05). Exercise training was as effective as tamoxifen treatment in decreasing serum estradiol and ER-α expression (P<0.05). Exercise training and tamoxifen reduced tumor IL-6 levels, NF-kB and STAT3 expressions, and up-regulated TPM1 and PDCD4 expressions (P<0.05). Both exercise and tamoxifen had synergistic effects in reducing miR-21 and Bcl-2, and up-regulating PDCD4 expression. Results showed that interval exercise training may reduce mammary tumor burden in mice through possible underlying pathway of miR-21.Entities:
Keywords: Breast cancer; Interval exercise training; Tamoxifen; miR-21
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Year: 2015 PMID: 26300395 DOI: 10.1016/j.ejphar.2015.08.031
Source DB: PubMed Journal: Eur J Pharmacol ISSN: 0014-2999 Impact factor: 4.432