GATA1 Expression in BCR/ABL1-negative Myeloproliferative Neoplasms

被引:3
|
作者
Yang, Naery [1 ]
Park, Sholhui [1 ]
Cho, Min-Sun [2 ]
Lee, Miae [1 ]
Hong, Ki-Sook [1 ]
Mun, Yeung Chul [3 ]
Seong, Chu-Myong [3 ]
Huh, Hee Jin [4 ]
Huh, Jungwon [1 ]
机构
[1] Ewha Womans Univ, Coll Med, Dept Lab Med, 1071 Anyangcheon Ro, Seoul 07985, South Korea
[2] Ewha Womans Univ, Coll Med, Dept Pathol, Seoul, South Korea
[3] Ewha Womans Univ, Coll Med, Dept Internal Med, Seoul, South Korea
[4] Dongguk Univ Ilsan Hosp, Dept Lab Med, 27 Dongguk Ro, Goyang 10326, South Korea
基金
新加坡国家研究基金会;
关键词
Polycythemia vera; Essential thrombocythemia; Prefibrotic primary myelofibrosis; Primary myelofibrosis; GATA1; BONE-MARROW BIOPSY; ESSENTIAL THROMBOCYTHEMIA; ALLELE BURDEN; PRIMARY MYELOFIBROSIS; POLYCYTHEMIA-VERA; JAK2; V617F; DIAGNOSIS; MUTATIONS; IMPACT; MEGAKARYOCYTES;
D O I
10.3343/alm.2018.38.4.296
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
Background: This study aimed to determine GATA1 expression levels to better characterize subgroups in BCR/ABL1-negative myeloproliferative neoplasms (MPNs). Methods: This study enrolled 49 patients diagnosed as having BCR/ABL1-negative MPN on the basis of the 2016 World Health Organization classification : nine polycythemia vera (PV), 17 essential thrombocythemia (ET), 12 prefibrotic primary myelofibrosis (prePMF), and 11 overt primary myelofibrosis (PMF). Relevant clinical and laboratory data were retrieved from the medical records. The molecular analysis of CALR and MPL mutations and quantification of JAK2 V617F allele burden were performed. GATA1 expression was assessed by an immunohistochemical assay on bone marrow biopsy. GATA1 expression was analyzed serially in 18 patients. Results: GATA1 expression decreased significantly in PMF compared with that in other subtypes, while no statistical difference was identified between ET and prePMF. GATA1 expression did not differ according to the mutation profiles or the allele burden of JAK2 V617F, but it decreased significantly in patients with overt fibrosis or leukemic transformation. Conclusions: Our results suggest that GATA1 expression is significantly low in PMF and decreases with progressive fibrosis and possibly with leukemic transformation, although our attempt to accurately distinguish between subgroups using GATA1 immunohistochemical approach did not achieve statistical significance. A large patient cohort with long term follow-up is required to evaluate the prognostic value of GATA1 expression.
引用
收藏
页码:296 / +
页数:12
相关论文
共 50 条
  • [11] Aberrant expression of SPAG6 may affect the disease phenotype and serve as a tumor biomarker in BCR/ABL1-negative myeloproliferative neoplasms
    Ding, Li
    Luo, Jie
    Zhang, Jing
    Wang, Ji
    Li, Zhao
    Huang, Juan
    Chai, Li
    Mu, Jiao
    Zhao, Beibei
    Zhong, Yi
    Zhang, Lin
    Liu, Lin
    ONCOLOGY LETTERS, 2022, 23 (01)
  • [12] Differential diagnosis of BCR-ABL1-negative myeloproliferative neoplasms
    Kvasnicka, Hans Michael
    Griesshammer, Martin
    LABORATORIUMSMEDIZIN-JOURNAL OF LABORATORY MEDICINE, 2015, 39 (05): : 301 - 310
  • [13] Approach to Diagnosis of BCR::ABL1 -Negative Myeloproliferative Neoplasms
    Satiza, Manali
    Purohit, Abhishek H. L.
    INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2023, 44 (06) : 585 - 591
  • [14] BCR-ABL negative myeloproliferative neoplasms
    Metzgeroth, G.
    Lengfelder, E.
    Griesshammer, M.
    Reiter, A.
    ONKOLOGE, 2012, 18 (12): : 1130 - +
  • [15] Dominance of mutations in epigenetic regulators and a diversity of signaling alterations in blast-phase BCR::ABL1-negative myeloproliferative neoplasms
    Gurban, Petruta
    Mambet, Cristina
    Botezatu, Anca
    Necula, Laura G.
    Matei, Lilia
    Neagu, Ana Iulia
    Pitica, Ioana
    Ataman, Marius
    Tatic, Aurelia
    Bardas, Alexandru
    Gaman, Mihnea A.
    Dobrea, Camelia
    Dragomir, Mihaela
    Ghimici, Cecilia
    Angelescu, Silvana
    Barbu, Doina
    Stanca, Oana
    Danila, Marina
    Berbec, Nicoleta
    Colita, Andrei
    Vladareanu, Ana Maria
    Nedeianu, Saviana
    Chivu-Economescu, Mihaela
    Bleotu, Coralia
    Coriu, Daniel
    Sepulchre, Elise
    Anton, Gabriela
    Diaconu, Carmen C.
    Constantinescu, Stefan N.
    AMERICAN JOURNAL OF HEMATOLOGY, 2025, 100 (01) : 168 - 171
  • [16] BCR-ABL-negative myeloproliferative NeoplasienBCR-ABL negative myeloproliferative neoplasms
    G. Metzgeroth
    E. Lengfelder
    M. Griesshammer
    A. Reiter
    Der Onkologe, 2012, 18 (12): : 1130 - 1138
  • [17] Infections and vaccination in patients with BCR::ABL1 negative myeloproliferative neoplasms
    Haberbosch, S. M.
    Mertin, F.
    Hochhaus, A.
    Heidel, F.
    Hilgendorf, I
    Crodel, C. C.
    ONCOLOGY RESEARCH AND TREATMENT, 2023, 46 : 108 - 108
  • [18] Molecular genetics of BCR-ABL1 negative myeloproliferative neoplasms in India
    Rabade, Nikhil
    Subramanian, P. G.
    Kodgule, Rohan
    Raval, Goutham
    Joshi, Swapnali
    Chaudhary, Shruti
    Mascarenhas, Russel
    Tembhare, Prashant
    Gujral, Sumeet
    Patkar, Nikhil
    INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2018, 61 (02) : 209 - 213
  • [19] Pathogenesis of cardiovascular events in BCR-ABL1-negative myeloproliferative neoplasms
    Guy, Alexandre
    Poisson, Johanne
    James, Chloe
    LEUKEMIA, 2021, 35 (04) : 935 - 955
  • [20] Pathogenesis of cardiovascular events in BCR-ABL1-negative myeloproliferative neoplasms
    Alexandre Guy
    Johanne Poisson
    Chloe James
    Leukemia, 2021, 35 : 935 - 955