Genome-wide functions of PML–RARα in acute promyelocytic leukaemia

被引:0
|
作者
S Saeed
C Logie
H G Stunnenberg
J H A Martens
机构
[1] Faculty of Science,Department of Molecular Biology
[2] Nijmegen Centre for Molecular Life Sciences,undefined
[3] Radboud University,undefined
来源
British Journal of Cancer | 2011年 / 104卷
关键词
PML-RAR; RXR; PU.1 (SPI1); epigenome;
D O I
暂无
中图分类号
学科分类号
摘要
PML—RAR (retinoic acid receptor)α is the hallmark protein of acute promyelocytic leukaemia, a highly malignant subtype of acute myeloid leukaemia that accounts for approximately 10% of all AML cases. Recently, several studies have been set out to obtain a comprehensive genome-wide view of the molecular actions of this chimeric protein. In this review, we highlight the new insights that arose from these studies, in particular focussing on newly identified PML–RARα target genes, its interplay with RXR and deregulation of epigenetic modifications.
引用
收藏
页码:554 / 558
页数:4
相关论文
共 50 条
  • [21] Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
    Charles G. Mullighan
    Salil Goorha
    Ina Radtke
    Christopher B. Miller
    Elaine Coustan-Smith
    James D. Dalton
    Kevin Girtman
    Susan Mathew
    Jing Ma
    Stanley B. Pounds
    Xiaoping Su
    Ching-Hon Pui
    Mary V. Relling
    William E. Evans
    Sheila A. Shurtleff
    James R. Downing
    Nature, 2007, 446 : 758 - 764
  • [22] Acute promyelocytic leukemia:: A novel PML/RARα fusion that generates a frameshift in the RARα transcript and ATRA resistance
    Zayed, Adham
    Couban, Stephen
    Hayne, Ormille
    Sparavalo, Nebojsa
    Shawwa, Allam
    Sadek, Irene
    Greer, Wenda
    LEUKEMIA & LYMPHOMA, 2007, 48 (03) : 489 - 496
  • [23] Acute promyelocytic leukemia with amplification of PML-RARα rearrangement: Clinical implications
    Luatti, Simona
    Marzocchi, Giulia
    Ottaviani, Emanuela
    Baldazzi, Carmen
    Stacchini, Monica
    Gamberini, Carla
    Salmi, Federica
    Martinelli, Giovanni
    Baccarani, Michele
    Testoni, Nicoletta
    LEUKEMIA RESEARCH, 2008, 32 (12) : 1941 - 1943
  • [24] Pretreatment characteristics and clinical outcome of acute promyelocytic leukaemia patients according to the PML-RARα isoforms:: a study of the PETHEMA group
    González, M
    Barragán, E
    Bolufer, P
    Chillón, C
    Colomer, D
    Borstein, R
    Calasanz, MJ
    Gómez-Casares, MT
    Villegas, A
    Marugán, I
    Román, J
    Martín, G
    Rayón, C
    Debén, G
    Tormo, M
    Díaz-Mediavilla, J
    Esteve, J
    González-San Miguel, J
    Rivas, C
    Pérez-Equiza, K
    García-Sanz, R
    Capote, FJ
    Ribera, JM
    Arias, J
    León, A
    Sanz, MA
    BRITISH JOURNAL OF HAEMATOLOGY, 2001, 114 (01) : 99 - 103
  • [25] PML/RARα(+) hypergranular acute promyelocytic leukemia (M3) developing into an M3 acute myelocytic leukemia without PML/RARα
    Ruiz-Argüelles, GJ
    Ruiz-Delgado, GJ
    Reyes-Núñez, V
    ACTA HAEMATOLOGICA, 2000, 104 (2-3) : 124 - 127
  • [26] Coexistence of PML-RARα and BCR-ABL in acute promyelocytic leukemia
    Pettijohn, Erin M.
    Platanias, Leonidas C.
    Altman, Jessica K.
    LEUKEMIA & LYMPHOMA, 2014, 55 (02) : 238 - 239
  • [27] Pathogenetic role of the PML/RAR alpha fusion protein in acute promyelocytic leukemia
    Grignani, F
    Pelicci, PG
    MOLECULAR ASPECTS OF MYELOID STEM CELL DEVELOPMENT, 1996, 211 : 269 - 278
  • [28] PML-RARα/RXR Alters the Epigenetic Landscape in Acute Promyelocytic Leukemia
    Martens, Joost H. A.
    Brinkman, Arie B.
    Simmer, Femke
    Francoijs, Kees-Jan
    Nebbioso, Angela
    Ferrara, Felicetto
    Altucci, Lucia
    Stunnenberg, Hendrik G.
    CANCER CELL, 2010, 17 (02) : 173 - 185
  • [29] CLINICAL RELEVANCE OF THE PML-RAR-A GENE REARRANGEMENT IN ACUTE PROMYELOCYTIC LEUKEMIA
    LOCOCO, F
    PELICCI, PG
    BIONDI, A
    LEUKEMIA & LYMPHOMA, 1994, 12 (5-6) : 327 - 332
  • [30] FUSION PROTEINS BETWEEN PML AND RAR-ALPHA IN ACUTE PROMYELOCYTIC LEUKEMIA
    KASTNER, P
    PEREZ, A
    LUTZ, Y
    ROCHETTEEGLY, C
    GAUB, MP
    CHAMBON, P
    COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES, 1991, 185 (06): : 391 - 401