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<STUDY_SET>
    <STUDY accession="DRP002367" center_name="HIROSHIMA" alias="DRP002367">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB3156</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>Collaborative effects of SETBP1-D868N with ASXL1-MT in inducing AML</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>Using a mouse BMT model, we examined the in vivo effect of simultaneous expression of ASXL1-MT and SETBP1-D868N. All of the mice transplanted with BM cells expressing both ASXL1-MT and SETBP1-D868N died of acute leukemia after a short latency, while all of the mice transplanted with BM cells expressing either ASXL1-MT or SETBP1-D868N alone survived for 6 months after transplantation. To elucidate the mechanism for leukemogenesis induced by the combination of ASXL1-MT and SETBP1-D868N, we compared the expression profile of BM cells of AML mice induced by both ASXL1-MT and SETBP1-D868N with that of BM cells of MDS mice induced by ASXL1-MT.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>Collaborative effects of SETBP1-D868N with ASXL1-MT in inducing AML</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB3156</ID>
                        <LABEL>PRJDB3156</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>Using a mouse BMT model, we examined the in vivo effect of simultaneous expression of ASXL1-MT and SETBP1-D868N. All of the mice transplanted with BM cells expressing both ASXL1-MT and SETBP1-D868N died of acute leukemia after a short latency, while all of the mice transplanted with BM cells expressing either ASXL1-MT or SETBP1-D868N alone survived for 6 months after transplantation. To elucidate the mechanism for leukemogenesis induced by the combination of ASXL1-MT and SETBP1-D868N, we compared the expression profile of BM cells of AML mice induced by both ASXL1-MT and SETBP1-D868N with that of BM cells of MDS mice induced by ASXL1-MT.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
