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1.
Indian J Cancer ; 2014 Jul-Sep; 51(3): 358-362
Article in English | IMSEAR | ID: sea-154419

ABSTRACT

Background: Colorectal cancer is one of the most common causes of death in the world and third and fourth most common cancer among men and women in Iran respectively. Epidermal growth factor receptor (EGFR) is a tyrosine kinase receptor that shows over expression in epithelial tumors and regulates important processes in tumorigenesis. Incidence and characteristics of colorectal cancer are based on the geographic region and race. Aim: In this research work, the over expression of EGFR in formalin fixed paraffin-embedded (FFPE) colorectal cancer tumor tissue of patients was studied. Materials and Methods: Fifteen FFPE colorectal cancer tumor tissues (10 women and 5 men; 25-65 years old and stage IV) and 15 non-patients (nine women and six men; 25-65 years old) that were collected during 2006-2012. EGFR gene expression level was analyzed by real-time quantitative reverse transcriptase polymerase chain reaction (PCR). All PCR reactions were performed in triplicate for both target gene and internal control (18s ribosomal ribonucleic acid) with the 2−ΔΔCT method. Gene expression differences in patients and controls were evaluated with t-test. Results: The results were showed EGFR gene over expression in 12 (80%) of 15 patients. There was a statistically significant difference in the prevalence of EGFR expression between patients and control (P < 0.05). Conclusion: Our results demonstrated EGFR gene over expression in colorectal cancer tumor tissue compared with controls.


Subject(s)
Colorectal Neoplasms/genetics , Fixatives , Formaldehyde , Gene Expression/genetics , Gene Expression Profiling , Humans , Male , Paraffin Embedding , ErbB Receptors/genetics , Reverse Transcriptase Polymerase Chain Reaction , Tissue Fixation
2.
Braz. j. microbiol ; 41(1): 82-90, Jan.-Mar. 2010. ilus, graf
Article in English | LILACS | ID: lil-531738

ABSTRACT

In this study, we investigated the binding ability of Saccharomayces cerevisiae to aflatoxin in pistachio nuts. The obtained results indicate that S. cerevisiae has an aflatoxin surface binding ability of 40 percent and 70 percent (with initial aflatoxin concentrations of 10 and 20 ppb) in the exponential phase. Acid treatments increase this ability to approximately 60 percent and 73 percent for the two concentrations of aflatoxin, respectively. Heat treatments also enhance surface binding to 55 percent and 75 percent, respectively. Binding appears to be a physical phenomenon that saturates within the first 2-3 hours of the process. The obtained results indicate that yeast immobilization for toxin reduction on aflatoxin-contaminated pistachios had no effect on qualitative characteristics, such as color, texture, and peroxide value. Yeast cells, viable or nonviable, are effective for aflatoxin binding, and this property could lead to a promising solution to aflatoxin contamination in high-risk foods.


Subject(s)
Aflatoxins/analysis , Aflatoxins/isolation & purification , Biological Phenomena , Pistacia , Saccharomyces cerevisiae/isolation & purification , Food Contamination , Food Samples , Methods , Methods , Toxicity
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