Breast Cancer Synthesis

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Title: Altered HOX gene expression in Breast Cancer Introduction It is a very fascinating thought that a single cell zygote contains all information required for the development of an organism. HOX genes called Homeobox are family of 39 transcription factors divided into 4 clusters A, B, C and D and are located on different chromosomes 7p15, 17q21.2, 12q13 and 2q31 (De Souza et al., 2010). HOX genes control the body plan of embryo along anterior-posterior axis and are expressed during embryonic development in highly coordinated manner and continue to express in virtually all tissues and organ throughout adult life (Terence et al., 2006). In addition of its role in development and subsequently in stem cell differentiation the HOX genes are …show more content…

Ninety percent of deaths from tumor are due to metastasis making the pathophysiology of this process and study of genes involved regulating metastasis central to understand the mechanism of this disease (Boimel et al., 2011). Breast cancer seems to originate from changes in the architectural breast tissue organization consequent to interaction between cell genome and extracellular environment. Thus basic cellular processes and their molecular regulation play an important role on the onset of breast cancer. Various transcription factors are involved in regulation and expression of specific genes crucial for cellular mechanism; any alteration in these mechanisms may give rise to series of malignancies including breast cancer (Cantilte et al., …show more content…

Conversely overexpression of HOXB2 ORF in MDA-MB-231 and MTLn3-ErB1 breast cancer lines reduced primary tumor growth with increased percentage of cells in mitosis in HOXB2 shRNA tumors and decreased mitosis in HOXB2 ORF tumors compared to empty vector control. However the effects on in vitro growth properties were not significantly different from control with no significant difference in in vitro survival with HOXB2 knockdown, indicating an in vivo specific effect that may be dependent on the tumor microenvironment. A small increase in invasiveness of cells suppressed in expression of HOXB2 contributed to the possibility that increase in invasion may contribute to increase in vivo growth rate (Boimel et al.,

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