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Journal of the Arab Society for Medical Research. 2018; 13 (2): 113-118
em Inglês | IMEMR | ID: emr-202950

RESUMO

Background/aim: Breast carcinoma is a common, yet heterogeneous aggressive disease affecting relatively young patients. The androgen receptor [AR] is expressed in majority of breast cancers and across the main breast cancer subtypes. The aim of this study was to evaluate AR expression in hormone-negative breast cancer subtypes


Materials and methods: Sixty cases of breast cancer were involved in this study; the samples were received in the Department of Pathology of Kasr El-Aini Hospital, Cairo University, Egypt. The expression of AR and human epidermal growth factor receptor-2 receptors were studied by immunohistochemistry in 60 formalin-fixed paraffin-embedded selected hormone-negative breast cancer surgical specimens. The immunohistochemistry expression of the marker was correlated with the clinicopathological variables


Results: Of the hormone-negative cases, 61.6% show positive AR expression, 89% of which are invasive duct carcinoma, 68.3% are associated with ductal carcinoma in situ, and 55% are human epidermal growth factor receptor-2-enriched subtype. A significant correlation was found between the AR expression and tumor type. There is no evident significant correlation with tumor grade, multicentricity or lymphovascular invasion


Conclusion: The AR has recently emerged as a useful marker for the further refinement of breast cancer subtype classification. Antiandrogens are thought to markedly enhance treatments and to be the first targeted therapy in hormone-negative breast cancer cases

2.
Journal of the Arab Society for Medical Research. 2018; 13 (2): 129-143
em Inglês | IMEMR | ID: emr-202952

RESUMO

Background/aim: Liver fibrosis and its end-stage cirrhosis are the main reasons of morbidity and mortality all over the world. The current study aimed to evaluate the efficacy of Zilla spinosa [Z. spinosa] on CCl4-induced liver fibrosis, apoptosis, and oxidative stresses in rats


Materials and methods: Extract of aerial part of Z. spinosa was used in this study. Thirty male Sprague Dawley rats were enrolled in this study and divided into five groups [six each]: group 1 served as control and groups 2-5 were treated with CCl4 [1ml/kg intraperitoneal twice a week for 8 weeks], where group 2 served as a control positive, group 3 received silymarin [50?mg/kg] daily, and groups 4 and 5 were administrated with Z. spinosa [100 and 200 mg/kg, respectively] daily for 8 weeks. At the end of each experiment, liver function tests were analyzed in serum, whereas malondialdehyde [MDA], Nitric oxide [NO], Glutathione [GSH], and hydroxyproline [HA] were analyzed in liver tissues. Liver fibrosis was confirmed histopathologically, and collagen content, caspase-3, and alpha-smooth muscle actin [alpha-SMA] were assayed immunhistochemically


Results: Alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, total bilirubin, MDA, NO, and HA levels were increased [P<0.05], whereas total protein and GSH were decreased [P<0.05] in CCl4-administrated rats. Histopathological results showed loss of lobular structure, fibrosis with expansion of portal tract by fibrous tissue together with inflammatory changes confined to portal tract and central vein, and intense centrilobular necrosis and remarkable fatty hydropic degeneration. In addition, extensive accumulation of connective tissue, marked depletion of glycogen, strong expression of alpha-SMA, and increased of caspase-3 were found in CCl4-administrated rats. Oral administration of Z. spinosa at 100 or 200 mg/kg restored the normal levels of liver function parameters, MDA, NO and GSH; decreased HA; and reduced collagen, glycogen content, caspase-3, and alpha-SMA in liver tissue of rats. The high dose of 200 mg/kg showed more potent effect than low dose of 100 mg/kg when compared with silymarin treatment group


Conclusion:The present study clarified that Z. spinosa extract has antioxidant and antiapoptotic properties in CCl4-induced liver fibrosis in rats, and may be able to exert a therapeutic effect on developing hepatic fibrosis; moreover, high dose of 200?mg/kg appeared to be more potent than low dose [100 mg/kg]

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