Endometrial cancer remains to be a major type of malignancy in threatening female life.Molecular insights in advancing our understanding of endometrial tumorigenesis are much needed.We here report that a less-studied ...Endometrial cancer remains to be a major type of malignancy in threatening female life.Molecular insights in advancing our understanding of endometrial tumorigenesis are much needed.We here report that a less-studied protein Dihydropyrimidinase like 3(DPYSL3)is a potent tumor suppressor.DPYSL3 is uniquely regulated by wild type p53(wtp53),and its expression is at the highest level when cells carry wtp53 and are exposed to hypoxia.We reveal that wtp53 can bind DPYSL3 promoter to enhance DPYSL3 expression and in turn,the elevated DPYSL3 can restrain cancer cell proliferation and invasion in vitro and in vivo.Importantly,we observe that DPYSL3 can interfere with MAP kinase pathway,supported by a substantially reduced level of phosphorylated ERK in cells with high expression of DPYSL3.Furthermore,we identify the specific region of DPYSL3 that is responsible for its interaction with MEK and a subsequently reduced activity of ERK.In combination of molecular docking and mutagenesis analysis,we validated that the therapeutic implication of 17 A.A.s of DPYSL3,which can reduce the activity of the MAPK pathway and inhibit endometrial tumor cell growth in vitro and in vivo.Therefore,our study not only demonstrates in-depth understanding of human tumorigenesis,especially endometrial tumor,but also only provides a therapeutic potential to develop an effective tool to fight against human malignancy.展开更多
文摘Endometrial cancer remains to be a major type of malignancy in threatening female life.Molecular insights in advancing our understanding of endometrial tumorigenesis are much needed.We here report that a less-studied protein Dihydropyrimidinase like 3(DPYSL3)is a potent tumor suppressor.DPYSL3 is uniquely regulated by wild type p53(wtp53),and its expression is at the highest level when cells carry wtp53 and are exposed to hypoxia.We reveal that wtp53 can bind DPYSL3 promoter to enhance DPYSL3 expression and in turn,the elevated DPYSL3 can restrain cancer cell proliferation and invasion in vitro and in vivo.Importantly,we observe that DPYSL3 can interfere with MAP kinase pathway,supported by a substantially reduced level of phosphorylated ERK in cells with high expression of DPYSL3.Furthermore,we identify the specific region of DPYSL3 that is responsible for its interaction with MEK and a subsequently reduced activity of ERK.In combination of molecular docking and mutagenesis analysis,we validated that the therapeutic implication of 17 A.A.s of DPYSL3,which can reduce the activity of the MAPK pathway and inhibit endometrial tumor cell growth in vitro and in vivo.Therefore,our study not only demonstrates in-depth understanding of human tumorigenesis,especially endometrial tumor,but also only provides a therapeutic potential to develop an effective tool to fight against human malignancy.
