Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome

被引:37
|
作者
Chen, C-Y [1 ]
Lin, L-I
Tang, J-L
Tsay, W.
Chang, H-H
Yeh, Y-C
Huang, C-F
Chiou, R-J
Yao, M.
Ko, B-S
Chen, Y-C
Lin, K-H
Lin, D-T
Tien, H-F
机构
[1] Natl Taiwan Univ, Coll Med, Dept Internal Med, Taipei 10018, Taiwan
[2] Natl Taiwan Univ, Coll Med, Dept Lab Med, Taipei 10018, Taiwan
[3] Natl Taiwan Univ, Coll Med, Dept Clin Sci & Med Biotechnol, Taipei 10018, Taiwan
[4] Natl Taiwan Univ, Coll Med, Dept Pediat, Taipei 10764, Taiwan
关键词
D O I
10.1038/sj.leu.2404190
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:1155 / 1158
页数:4
相关论文
共 48 条
  • [1] Acquisition of JAK2, PTPN11, and RAS mutations during disease progression in primary myelodysplastic syndrome
    C-Y Chen
    L-I Lin
    J-L Tang
    W Tsay
    H-H Chang
    Y-C Yeh
    C-F Huang
    R-J Chiou
    M Yao
    B-S Ko
    Y-C Chen
    K-H Lin
    D-T Lin
    H-F Tien
    Leukemia, 2006, 20 : 1155 - 1158
  • [2] Acquisition of RAS and JAK2 mutations contributes to progression of CMML from the dysplastic to the proliferative variant
    Onida, F.
    Ricci, C.
    Fermo, E.
    Miranda, C.
    Corti, S.
    Cortelezzi, A.
    Fariciotti, A.
    Soligo, D.
    Deliliers, G. Lambertenghi
    LEUKEMIA RESEARCH, 2007, 31 : S81 - S82
  • [3] Acquisition of Receptor Tyrosine Kinases, JAK2, or Ras Pathway Mutations Is Associated with Acute Myeloid Leukemia Transformation In Patients with Myelodysplastic Syndrome
    Lin, Tung-Liang
    Kuo, Ming-Chung
    Liang, Der-Cherng
    Huang, Chein-Fuang
    Lin, Tung-Huei
    Lee, En-Hui
    Shih, Yu-Shu
    Wu, Jin-Hou
    Shih, Lee-Yung
    BLOOD, 2010, 116 (21) : 1640 - 1640
  • [4] JAK2 and PTPN11 mutations as potential biomarkers for BCL-xL inhibition as monotherapy and in combination therapy for acute myeloid leukemia
    Bellin, Richard J.
    Hilgenberg, Valerie
    Popovic, Relja
    Uziel, Tamar
    Lam, Lloyd T.
    CANCER RESEARCH, 2017, 77
  • [5] LOSS OF MULTIPLE POINT MUTATIONS OF RAS GENES ASSOCIATED WITH ACQUISITION OF CHROMOSOMAL-ABNORMALITIES DURING DISEASE PROGRESSION IN MYELODYSPLASTIC SYNDROME
    NAKAGAWA, T
    SAITOH, S
    IMOTO, S
    ITOH, M
    TSUTSUMI, M
    HIKIJI, K
    NAKAO, Y
    FUJITA, T
    BRITISH JOURNAL OF HAEMATOLOGY, 1991, 77 (02) : 250 - 252
  • [6] PTPN11/SH2 gene mutations and linear growth in Noonan syndrome
    Giordani, Lucia
    Faienza, Maria Felicia
    Acquafredda, Angelo
    Zecchino, Clara
    Vivenza, Daniela
    Delvecchio, Maurizio
    Cavallo, Luciano
    HORMONE RESEARCH, 2006, 65 : 69 - 69
  • [7] Coexisting PTPN11 and TNNT2 mutations in noonan syndrome with multiple lentigines
    Liu, H.
    Han, X.
    Chu, S.
    Ma, W.
    Ding, W.
    Li, J.
    Jiang, Y.
    QJM-AN INTERNATIONAL JOURNAL OF MEDICINE, 2024, 117 (06) : 460 - 461
  • [8] Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome
    Bowen, Margot E.
    Boyden, Eric D.
    Holm, Ingrid A.
    Campos-Xavier, Belinda
    Bonafe, Luisa
    Superti-Furga, Andrea
    Ikegawa, Shiro
    Cormier-Daire, Valerie
    Bovee, Judith V.
    Pansuriya, Twinkal C.
    de Sousa, Sergio B.
    Savarirayan, Ravi
    Andreucci, Elena
    Vikkula, Miikka
    Garavelli, Livia
    Pottinger, Caroline
    Ogino, Toshihiko
    Sakai, Akinori
    Regazzoni, Bianca M.
    Wuyts, Wim
    Sangiorgi, Luca
    Pedrini, Elena
    Zhu, Mei
    Kozakewich, Harry P.
    Kasser, James R.
    Seidman, Jon G.
    Kurek, Kyle C.
    Warman, Matthew L.
    PLOS GENETICS, 2011, 7 (04):
  • [9] Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia
    Matsuda, Kazuyuki
    Sakashita, Kazuo
    Taira, Chiaki
    Tanaka-Yanagisawa, Miyuki
    Yanagisawa, Ryu
    Shiohara, Masaaki
    Kanegane, Hirokazu
    Hasegawa, Daiichiro
    Kawasaki, Keiichiro
    Endo, Mikiya
    Yajima, Shuhei
    Sasaki, Shinya
    Kato, Keisuke
    Koike, Kazutoshi
    Kikuchi, Akira
    Ogawa, Atsushi
    Watanabe, Akihiro
    Sotomatsu, Manabu
    Nonoyama, Shigeaki
    Koike, Kenichi
    BRITISH JOURNAL OF HAEMATOLOGY, 2010, 148 (04) : 593 - 599
  • [10] Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome
    Tartaglia, M
    Mehler, EL
    Goldberg, R
    Zampino, G
    Brunner, HG
    Kremer, H
    van der Burgt, I
    Crosby, AH
    Ion, A
    Jeffery, S
    Kalidas, K
    Patton, MA
    Kucherlapati, RS
    Gelb, BD
    NATURE GENETICS, 2001, 29 (04) : 465 - 468