we performed xenograft experiments in NIH-III nude mice using HCT116 cells which either stably overexpress SBP1 or a control vector. Four weeks after cancer cell injection, tumors were isolated and tumor volume and weight was determined. SBP1 expression in explanted tumors derived from SBP1 overexpressing HCT116 cells was confirmed via RT-PCR showing 607-fold increase at mRNA level. Consistent with in vitro data, mice injected with SBP1 overexpressing HCT116 cells had a significantly smaller tumor volume and tumor weight than the mice injected with control cells, indicating that SBP1 has tumor suppressive functions in vivo as well. Taken above, we provide the first evidence that SBP1 promoter is hypermethylated in human colorectal cancer, and that demethylation via DAC increases SBP1 promoter activity as well as rescuing mRNA and protein expression. Gene silencing is a common mechanism found in many human cancers to inhibit tumor suppressor expression. Our data show that the SBP1 promoter is highly methylated in tumor tissues of colorectal cancer patients, indicating that SBP1 expression in colon cancer is in part controlled through gene silencing. It is critical to investigate whether SBP1 gene silencing is a common mechanism to reduce SBP1 expression in other types of cancer in which SBP1 has been shown to be MCE Company 84573-16-0 downregulated. Moreover, due to decreased expression of SBP1 in human cancers, SBP1 has been suggested to have tumor suppressive NSC 601980 activities. We believe that we are the first ones to provide evidence that this may indeed be true, in terms of that overexpression of SBP1 in HCT116 cells suppressed cell proliferation, increased apoptotic cell death and decreased cell migration in vitro, and inhibited tumor growth in vivo. However, the exact mechanisms of SBP1 regulation and anti-cancer action remain unknown and need further investigation. In fact, it is currently being investigated in our laboratory. Understanding the regulation and mechanisms of SBP1 tumor suppressor functions will have a great impact in revealing the molecular mechanism of carcinogenesis and in developing more effective chemoprevention and chemotherapies for human malignant diseases. There is growing evidence of an impaired inn
