{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T14:00:35Z","timestamp":1790863235450,"version":"4.1.0"},"reference-count":25,"publisher":"American Society of Hematology","issue":"4","content-domain":{"domain":["ashpublications.org"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2002,2,15]]},"abstract":"<jats:p>While studying Ikaros proteins in childhood acute myeloid leukemia (AML), Ikaros isoform 6 (Ik6) expression was detected in 7 of 10 cases of M4 and M5 leukemia, but in none of the remaining French-American-British subtypes (M2, 8 cases; M7, 6 cases). The spliced Ikaros isoforms 4 to 8 (Ik4-8) suppress the function of full-length Ik1 or Ik2 in a dominant-negative manner, owing to their reduced numbers of DNA binding sites. Thus, dominant-negative Ikaros isoforms may inhibit the normal transcriptional regulation of hematopoietic cell development. To clarify the function of Ik6 in developing blood cells, this isoform was transiently transfected into an Ik2+, interleukin-3 (IL-3)\u2013dependent 32D murine myeloid precursor cell line and studied the expression of Bcl-2 family proteins in relation to in vitro cell growth, using a tetracycline-inducible TREx system. The possibility of aberrant cell regulation due to Ikaros functional changes was examined by cotransfecting both Ik2 and Ik6 into Ikaros\/Aiolos\/Helios triple-negative Cos-7 cells. The results demonstrated IL-3\u2013independent growth by Ik6-transfected 32D clones coincident with up-regulation of the antiapoptotic protein Bcl-XL. Up-regulation of Bcl-XL, but not of other Bcl-2 family proteins, was associated with the suppression of functional Ik2 by Ik6 in a dominant-negative fashion. Thus, the pathogenesis of myelomonocytic\/monocytic AML may involve aberrant regulation of apoptosis due to unscheduled expression of the Ik6 isoform.<\/jats:p>","DOI":"10.1182\/blood.v99.4.1350","type":"journal-article","created":{"date-parts":[[2002,7,27]],"date-time":"2002-07-27T12:46:40Z","timestamp":1027774000000},"page":"1350-1355","update-policy":"https:\/\/doi.org\/10.1182\/blood.2019cm0000","source":"Crossref","is-referenced-by-count":67,"title":["High frequency of Ikaros isoform 6 expression in acute myelomonocytic and monocytic leukemias: implications for up-regulation of the antiapoptotic protein Bcl-XL in leukemogenesis"],"prefix":"10.1182","volume":"99","author":[{"given":"Tomohito","family":"Yagi","sequence":"first","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shigeyoshi","family":"Hibi","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mami","family":"Takanashi","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gen","family":"Kano","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasuhiro","family":"Tabata","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Toshihiko","family":"Imamura","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tohru","family":"Inaba","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and 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Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shinsaku","family":"Imashuku","sequence":"additional","affiliation":[{"name":"From the Department of Pediatrics, Department of Clinical Laboratory and Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan; and Kyoto City Institute of Health and Environmental Sciences, Kyoto, Japan."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"234","reference":[{"key":"2020021221423159400_B1","doi-asserted-by":"crossref","first-page":"808","DOI":"10.1126\/science.1439790","article-title":"Ikaros, an early lymphoid-specific transcription factor and a putative mediator for T cell commitment.","volume":"258","author":"Georgopoulos","year":"1992","journal-title":"Science."},{"key":"2020021221423159400_B2","doi-asserted-by":"crossref","first-page":"143","DOI":"10.1016\/0092-8674(94)90407-3","article-title":"The Ikaros gene is required for the development of all lymphoid 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