Page 2 - D. Cancer biology
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[D. Cancer biology-1]



                    Understanding functional roles of FAM86A in NF-kB


                             mediated gastric tumorigenic responses




          Yo Han Hong¹, Jieun Oh¹, Wooram Choi¹, Han Gyung Kim¹, Deok Jeong¹, Chaoran Song¹, Long You¹,

                                                     Jae Youl Cho¹˙*


                           ¹Integrative biotechnology, Sungkyunkwan University, Suwon 16419, Korea




        FAM86A as a non-histone protein lysine methyltransferase has novelty and conserved sequence in the various

        species. In this study, we investigated functional roles of FAM86A on the gastric tumorigenic responses. According
        to  microarray  analysis  against  Asian  Cancer  Research  Group,  FAM86A was significantly overexpressed  in tumor

        compared to normal. Also, FAM86A overexpressed gastric cancer patient’s prognosis was known to be worse than
        control group. FAM86A was occurred genetic alteration in the cancer patients. FAM86A was overexpressed in most

        gastric tumor tissue and cancer cell lines. Moreover, FAM86A involved in various tumorigenic responses including
        cell proliferation, cell cycle, invasion, migration and colony formation. And then, we figured out the mechanism by

        which FAM86A regulates gastric tumorigenic responses. As results, FAM86A activated FGFR1, a novel binder partner
        of FAM86A, mediated NF-kB signaling pathway by the methylation dependent manner. FAM86A regulated tumor

        growth and metastasis in vivo mice model. These results suggest that FAM86A could regulate gastric tumorigenic
        responses through FGFR1 mediated NF-kB signaling pathway by the methylation dependent manner.
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