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Enayatollah Asadmanesh, Maryam Koushkie Jahromi, Farhad Daryanoosh, Javad Neamati, Zahra Mojtahedi,
Volume 9, Issue 3 (9-2019)
Abstract

Background & Objective: Many cancer patients suffer from cachexia or cancer-induced muscle atrophy. Cachexia can have various causes one of which is the reduction of muscle regeneration. Resistance training has been suggested as one of the proper stimulator of increasing muscular regeneration. The present study aimed at evaluating the effect of resistance training on two factors of regeneration including PAX7 and eMHC, tumor-free weight and tumor weight of mice. 
Materials & Methods: This study was a kind of experimental intervention. Subjects of the study included 10 BALB-C mice (age: 6 weeks) which CT-26  tumor was transplanted to them. Mice were divided into two groups of resistance training (n=5) and control (n=5) randomly. Training group performed six-week progressive resistance training and control groups were kept in cages without any exercise intervention. At the end of the experiment, gastrocnemius muscle was taken for evaluating related factors. Data were analyzed using the independent t-test.
Results: There was no significant difference in PAX7 between two groups of training and control, but eMHC reduced significantly in training compared to the control group (P=0.038). Tumor-free bodyweight of training group increased significantly compared to the control group (P=0.0004) and there was no significant difference in tumor weight between two groups of training and control.
Conclusion: Although resistance training does not increase tumor growth but probably reduce some muscle regeneration factors in cancer-bearing mice. So, for improving muscular regeneration in cachexia bearing patients, probably resistance training is not a good choice. However, more future researches are required.

Mahsa Behjati Moghaddam, Ali Neamati, Pouran Ardalan,
Volume 9, Issue 4 (11-2019)
Abstract

 Background & Objective: Cancer is a kind of genetic disease caused by DNA mutation which makes disorder in normal pattern of division and differentiation of cells and eventually formation of a neoplasm. Breast cancer is the most common malignancy and the second leading cause of death in women aged 35-55 years. Surgery, radiotherapy and chemotherapy are the common methods of controlling cancer, but the side effects and lack of positive results especially in metastatic tumors has led us discover new treatments. Nowadays, nanotechnology has helped us to find and develop new therapies. The purpose of this study was to characterize the antioxidant and apoptotic properties of zinc oxide nanoparticles biosynthesized by Amaranthus cruentus plant on breast cancer cells (MDA-MB-231).
Materials & Methods: The Zinc oxide nanoparticles were green-synthesized by the extract of Amaranthus cruentus leaves. Size and morphological characteristics of ZnO NPs determined by DLS tests, FESEM and TEM. To investigate the effect of ZnO nanoparticles on induction apoptosis, cancer cells were seeded in T25 flasks and treated with different concentrations of nanoparticles (15, 30 and 60 μg/ml). After 48 hours, gene expression changes of Bax and Bcl-2 was investigated by Real time PCR technique. SPSS software and one-way ANOVA test were used to analyze the data. At the end, comparison of means did by least significant differences (LSD) method.
Results: The DLS test showed the average size of the synthesized ZnO NPs is about 30 to 38 nm. The results of gene expression by Real time PCR technique showed that ZnO nanoparticles reduced anti-apoptosis gene expression Bcl-2 and increases pro-apoptotic gene expression in MDA cell line.
Conclusion: In general, the results obtained from this study can claim that ZnO nanoparticles have anti-cancer properties and can be introduced after further studies as candidates for cancer treatment in the field of medicine and pharmacy.
 

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