Biography
Biography: Suraiya Rasheed
Abstract
Melanomas are a group of heterogeneous tumors that arise in the epithelial cells of the skin, eye, meninges and other parts of the body. Patients with highly malignant melanomas do not respond well to the conventional therapies because most of these tumors are detected aft er they have invaded multiple tissues. For a number of years, we have studied a highly malignant cat melanoma cell line (CT1413) and examined its genome-wide proteomes at diff erent stages of tumor growth by mass spectrometry. Subtractive proteomics analyses and comparisons of protein profi les of tumor cells with normal cat embryo fi broblasts and a human leukemia cells indicated that CT1413 had a unique profi le, which did not match any other cells. Extensive bioinformatics analysis of all proteins indicated that >95% of proteins expressed in this melanoma are similar to proteins that are normally expressed during the growth and development of mammalian embryos. Proteomics analyses of several single cell clones of the cat melanoma indicated that this is a clonal tumor which is most likely derived from a single embryonic stem cell that transformed into tumor cell due to abnormal cell signaling events during the embryonic development. Each of the clones tested in multiple experiments conducted over one year period exhibited embryonic proteins. Th is phenomenon is in contrast to many human cancer stem cells that are diff erent areas of the tumor mass and exhibit only a few stem cell markers. Our bioinformatics analyses have identifi ed proteins/enzymes and transcriptional regulators that are essential for diff erentiation of diff erent tissue types/organ systems, development of neural network in the brain and proteins that regulate self-renewal and maintain stemness in these tumor cells. Th ese proteins provide unique biomarkers for the early detection of malignant melanomas and/or as targets for the development of novel therapeutic strategies for treating stem-cellderived melanomas.