KIT Gene as an Angiogenesis Marker in Sporadic Breast Cancer
محل انتشار: هفدهمین همایش سالانه آسیب شناسی و طب آزمایشگاه
سال انتشار: 1394
نوع سند: مقاله کنفرانسی
زبان: انگلیسی
مشاهده: 443
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شناسه ملی سند علمی:
ACPLMED17_080
تاریخ نمایه سازی: 20 آبان 1397
چکیده مقاله:
Introduction: CD117 (KIT) is a type III receptor tyrosine kinase operating in cell signal transduction in several cell types. Normally KIT is activated (phosphorylated) by binding of its ligand, the stem cell factor. Phosphorylation cascade activation is followed by activation of various transcription factors that regulates apoptosis, cell differentiation, proliferation, and angiogenesis. Angiogenesis, the process of new blood vessel formation, plays a key role in both local tumor growth and distant metastasis in breast cancer. By inhibiting Angiogenesis Genes such as KIT gene, the suppression of malignant tumors such as breast cancer could be possible.Material and Methods: In this study, we investigated association between copy number variation of KIT gene and increased risk of Sporadic Breast Cancer in 30 female patients, using MLPA kit p354.Result: In this study 13% of patients had deletion in exon 1 of KIT, while other patients had no changes in KIT copy numbers.Discussion & Conclusions: CD117 (KIT) gene could be an important factor in cancer development, and in association with increased risk of developing sporadic breast cancer, as a result utilizing angiogenesis inhibitor drugs could suppress Sporadic Breast Cancer. Further studies with more detailed data are needed to verify these initial findings.
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نویسندگان
Maryam Rahimi
Genetics Research Center,University of Social Welfare and Rehabilitation Sciences,Tehran,Iran
Elahe Keyhani
Assistant Professor, Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
Farkhondeh Behjati
Genetics Research Center,University of Social Welfare and Rehabilitation Sciences,Tehran,Iran
Fereidoon Sirati
Mehrad General Hospital, Tehran, Iran