ABO Blood Group Antigen Changes in Acute Myeloid Leukemia and No Significant Association With RUNX1 and GATA2 Somatic Variants

被引：5
|
作者：
Jeong, In Hwa [1 ]
Seo, Ji Young [1 ]
Choi, Sooin [2 ]
Kim, Hyun-Young [1 ,3 ]
Cho, Duck [1 ,3 ]
机构：
[1] Sungkyunkwan Univ, Samsung Med Ctr, Dept Lab Med & Genet, Sch Med, Seoul, South Korea
[2] Soonchunhyang Univ, Hosp Bucheon, Dept Lab Med & Genet, Coll Med, Bucheon, South Korea
[3] Sungkyunkwan Univ, Samsung Med Ctr, Dept Lab Med & Genet, Sch Med, 81 Irwon Ro, Seoul 06351, South Korea
来源：
ANNALS OF LABORATORY MEDICINE | 2023年 / 43卷 / 06期
关键词：
DNA METHYLATION; PROMOTER;
D O I：
10.3343/alm.2023.43.6.635
中图分类号：
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：635 / 637
页数：3
相关论文
共 50 条
  • [1] RUNX1 and GATA2 Regulate the Expression of the SET Oncogene in Acute Myeloid Leukemia
    Pippa, Raffaella
    Dominguez, Ana
    Marcotegui, Nerea
    Malumbres, Raquel
    Guruceaga, Elizabeth
    Odero, Maria D.
    BLOOD, 2014, 124 (21)
  • [2] Reduction of blood group an antigen on erythrocytes in a patient with myelodysplastic syndrome harboring somatic mutations in RUNX1 and GATA2
    Hayakawa, Akira
    Sano, Rie
    Takahashi, Yoichiro
    Okawa, Takafumi
    Kubo, Rieko
    Harada, Megumi
    Fukuda, Haruki
    Yokohama, Akihiko
    Handa, Hiroshi
    Kawabata-Iwakawa, Reika
    Tsuneyama, Hatsue
    Tsukada, Junichi
    Kominato, Yoshihiko
    TRANSFUSION, 2022, 62 (02) : 469 - 480
  • [3] ACUTE MYELOID LEUKEMIA WITH SOMATIC RUNX1 VARIANTS IN DNA LIGASE IV DEFICIENCY
    Niizato, Daiki
    Isoda, Takeshi
    Hoshino, Akihiro
    Nishimura, Akira
    Tomomasa, Dan
    Washio, Kana
    Kamiya, Takahiro
    Kanegane, Hirokazu
    Morio, Tomohiro
    Takagi, Masatoshi
    PEDIATRIC BLOOD & CANCER, 2024, 71 : S20 - S20
  • [4] Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
    Homan, Claire C.
    Drazer, Michael W.
    Yu, Kai
    Lawrence, David M.
    Feng, Jinghua
    Arriola-Martinez, Luis
    Pozsgai, Matthew J.
    Mcneely, Kelsey E.
    Ha, Thuong
    Venugopal, Parvathy
    Arts, Peer
    King-Smith, Sarah L.
    Cheah, Jesse
    Armstrong, Mark
    Wang, Paul
    Bodor, Csaba
    Cantor, Alan B.
    Cazzola, Mario
    Degelman, Erin
    Dinardo, Courtney D.
    Duployez, Nicolas
    Favier, Remi
    Froehling, Stefan
    Rio-Machin, Ana
    Klco, Jeffery M.
    Kraemer, Alwin
    Kurokawa, Mineo
    Lee, Joanne
    Malcovati, Luca
    Morgan, Neil, V
    Natsoulis, Georges
    Owen, Carolyn
    Patel, Keyur P.
    Preudhomme, Claude
    Raslova, Hana
    Rienhoff, Hugh
    Ripperger, Tim
    Schulte, Rachael
    Tawana, Kiran
    Velloso, Elvira
    Yan, Benedict
    Kim, Erika
    NISC Comparative Sequencing Program, Amy P.
    Hsu, Amy P.
    Holland, Steven M.
    Phillips, Kerry
    Poplawski, Nicola K.
    Babic, Milena
    Wei, Andrew H.
    Forsyth, Cecily
    BLOOD ADVANCES, 2023, 7 (20) : 6092 - 6107
  • [5] Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41
    Brown, Anna L.
    Homan, Claire
    Drazer, Michael W.
    Yu, Kai
    Lawrence, David
    Feng, Jinghua
    Arriola-Martinez, Luis
    Pozsgai, Matthew
    McNeely, Kelsey
    Thuong Ha
    Venugopal, Parvathy
    Arts, Peer
    King-Smith, Sarah
    Cheah, Jesse J. C.
    Armstrong, Mark
    Bodor, Csaba
    Wang, Paul
    Cantor, Alan B.
    Cazzola, Mario
    Degelman, Erin
    DiNardo, Courtney D.
    Duployez, Nicolas
    Favier, Remi
    Frohling, Stefan
    Rio-Machin, Ana
    Klco, Jeffery M.
    Kramer, Alwin
    Kurokawa, Mineo
    Lee, Joanne
    Malcovati, Luca
    Morgan, Neil, V
    Natsoulis, Georges
    Owen, Carolyn
    Patel, Keyur P.
    Preudhomme, Claude
    Raslova, Hana
    Rienhoff, Hugh Young, Jr.
    Ripperger, Tim
    Schulte, Rachael
    Tawana, Kiran
    Velloso, Elvira Deolinda Rodrigues Pereira
    Yan, Benedict
    Sood, Raman
    Hsu, Amy
    Holland, Steven M.
    Phillips, Kerry
    Poplawski, Nicola
    Babic, Milena
    Kim, Erika M. Kwon
    Wei, Andrew H.
    BLOOD, 2022, 140 : 4030 - 4033
  • [6] MYC-dependent recruitment of RUNX1 and GATA2 on the SET oncogene promoter enhances PP2A inactivation in acute myeloid leukemia
    Pippa, Raffaella
    Dominguez, Ana
    Malumbres, Raquel
    Endo, Akinori
    Arriazu, Elena
    Marcotegui, Nerea
    Guruceaga, Elizabeth
    Odero, Maria D.
    ONCOTARGET, 2017, 8 (33) : 53989 - 54003
  • [7] Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA)
    Brown, Anna L.
    Hahn, Christopher N.
    Scott, Hamish S.
    BLOOD, 2020, 136 (01) : 24 - 35
  • [8] Comparison of mutational profiles and clinical outcomes in patients with acute myeloid leukemia with mutated RUNX1 versus acute myeloid leukemia with myelodysplasia-related changes with mutated RUNX1
    Nguyen, Lynh
    Zhang, Xiaohui
    Roberts, Evans
    Yun, Seongseok
    McGraw, Kathy
    Abraham, Ivo
    Song, Jinming
    Braswell, Diana
    Qin, Dahui
    Sallman, David A.
    Lancet, Jeffrey E.
    List, Alan F.
    Moscinski, Lynn C.
    Padron, Eric
    Zhang, Ling
    LEUKEMIA & LYMPHOMA, 2020, 61 (06) : 1395 - 1405
  • [9] Acute myeloid leukemia with GATA2 and WT1 mutations mimicking acute promyelocytic leukemia
    Chen, Hongwei
    Wang, Haiyang
    BLOOD, 2024, 143 (03) : 290 - 290
  • [10] Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia
    Eriksson, Anna
    Engvall, Marie
    Mathot, Lucy
    Osterroos, Albin
    Rippin, Martin
    Cavelier, Lucia
    Ladenvall, Claes
    Baliakas, Panagiotis
    CLINICAL CANCER RESEARCH, 2023, 29 (15) : 2826 - 2834
12345