Author/Authors :
mahmoudian, reihaneh alsadat mashhad university of medical sciences - immunology research center, avicenna research institute - division of human genetics, Mashhad, Iran , abbaszadegan, mohammad reza mashhad university of medical sciences - medical genetics research center, medical school, immunology research center, avicenna research institute - division of human genetics, Mashhad, Iran , forghanifard, mohammad mahdi islamic azad university, damghan branch - department of biology, Damghan, Iran , moghbeli, meysam mashhad university of medical sciences - immunology research center, avicenna research institute - division of human genetics, Mashhad, Iran , moghbeli, faezeh islamic azad university, mashhad branch - department biology, Mashhad, Iran , chamani, jamshidkhan islamic azad university, mashhad branch - faculty of sciences - department of biochemistry and biophysics, Mashhad, Iran , gholamin, mehran mashhad university of medical sciences - immunology research center, buali research institute, Mashhad, Iran
Abstract :
Background: Human Cripto-1, a member of the EGF-CFC family, is involved in embryonic development, embryonic stem cell maintenance, and tumor progression. It also participates in multiple cell signaling pathways including Wnt, Notch, and TGF-β. Remarkably, it is expressed in cancer stem cell (CSC) compartments, boosting tumor cell migration, invasion, and angiogenesis. Although Cripto-1 is overexpressed in a variety of human malignant tumors, its expression in esophageal squamous cell carcinoma (ESCC) remains unclear. Our aim in this study was to evaluate the possible oncogenic role of Cripto-1 in ESCC progression and elucidate its association with clinicopathological parameters in patients. Methods: In this study, Cripto-1 expression in 50 ESCC tissue samples was analyzed and compared to corresponding margin-normal esophageal tissues using quantitative real-time PCR. Results: Cripto-1 was overexpressed in nearly 40% of ESCC samples compared with normal tissue samples. Significant correlations were observed between Cripto-1 expression and tumor differentiation grade, progression stage, and location (p 0.05). Conclusions: Our results indicate that overexpression of Cripto-1 is involved in the development of ESCC. Further assessment will be necessary to determine the role of Cripto-1 cross talk in ESCC tumorigenesis.
Keywords :
Cancer stem cell , Cripto , 1 , ESCC , Expressional analysis , Real , time PCR
