The detection of KIT mutations in acute myeloid leukemia

被引:3
|
作者
Silva Machado, Luis Eduardo [1 ]
Rebello Pinho, Joao Renato [1 ]
Sitnik, Roberta [1 ]
Muto, Nair Hideko [1 ]
Rodrigues Pereira Velloso, Elvira Deolinda [1 ]
Petroni, Roberta Cardoso [1 ]
Campregher, Paulo Vidal [1 ]
机构
[1] HIAE, Hematol Serv, Sao Paulo, SP, Brazil
来源
EINSTEIN-SAO PAULO | 2012年 / 10卷 / 03期
关键词
Leukemia; myeloid; acute; Receptor protein-tyrosine kinase; Core binding factors; Gene expression;
D O I
10.1590/S1679-45082012000300005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: This study describes a new method used in the clinical laboratory at Hospital Israelita Albert Einstein to detect mutations in exons 8 and 17 of the KIT gene in patients with acute myeloid leukemia. Methods: Genomic DNA extraction was performed on 54 samples of peripheral blood or bone marrow from patients with acute myeloid leukemia. The extracted DNA was amplified by polymerase chain reaction and sequenced, and the fragments were analyzed. Results: Within the analyzed samples, we detected four mutations in exon 8, two mutations in exon 17, and mutations or a double mutation in one sample. Conclusion: The tests detecting mutations in exon 8 and 17 on the KIT gene were successfully standardized. The test is now included among the routine diagnostics employed for patients at Hospital Israelita Albert Einstein clinical laboratory.
引用
收藏
页码:286 / 291
页数:6
相关论文
共 50 条
  • [21] KIT activating mutations: incidence in adult and pediatric acute myeloid leukemia, and identification of an internal tandem duplication
    Beghini, A
    Ripamonti, CB
    Cairoli, R
    Cazzaniga, G
    Colapietro, P
    Elice, F
    Nadali, G
    Grillo, G
    Haas, OA
    Biondi, A
    Morra, E
    Larizza, L
    HAEMATOLOGICA, 2004, 89 (08) : 920 - 925
  • [22] Mutations in KIT and RAS are frequent events in pediatric core-binding factor acute myeloid leukemia
    Goemans, BF
    Zwaan, CM
    Miller, M
    Zimmermann, M
    Harlow, A
    Meshinchi, S
    Loonen, AH
    Hählen, K
    Reinhardt, D
    Creutzig, U
    Kaspers, GJL
    Heinrich, MC
    LEUKEMIA, 2005, 19 (09) : 1536 - 1542
  • [23] Nanopore Targeted Sequencing for Rapid Gene Mutations Detection in Acute Myeloid Leukemia
    Cumbo, Cosimo
    Minervini, Crescenzio Francesco
    Orsini, Paola
    Anelli, Luisa
    Zagaria, Antonella
    Minervini, Angela
    Coccaro, Nicoletta
    Impera, Luciana
    Tota, Giuseppina
    Parciante, Elisa
    Conserva, Maria Rosa
    Spinelli, Orietta
    Rambaldi, Alessandro
    Specchia, Giorgina
    Albano, Francesco
    GENES, 2019, 10 (12)
  • [24] FRAGMENT LENGTH ANALYSIS SCREENING FOR CEBPA MUTATIONS DETECTION IN ACUTE MYELOID LEUKEMIA
    Fuster, O.
    Barragan, E.
    Bolufer, P.
    Cervera, J.
    Such, E.
    Montesinos, P.
    Sanz, M. A.
    HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 : 18 - 18
  • [25] Highly Sensitive Detection of IDH2 Mutations in Acute Myeloid Leukemia
    Petiti, Jessica
    Rosso, Valentina
    Croce, Eleonora
    Franceschi, Vanessa
    Andreani, Giacomo
    Dragani, Matteo
    De Gobbi, Marco
    Lunghi, Monia
    Saglio, Giuseppe
    Fava, Carmen
    Lo Iacono, Marco
    Cilloni, Daniela
    JOURNAL OF CLINICAL MEDICINE, 2020, 9 (01)
  • [26] Rethinking the gold standard for recurrent DNA mutations detection in acute myeloid leukemia
    Zago Novaretti, Marcia Cristina
    EUROPEAN JOURNAL OF HAEMATOLOGY, 2016, 96 (02) : 109 - 110
  • [27] Clinical Assay Design for Detection of CEBPA Mutations in Patients with Acute Myeloid Leukemia
    Deucher, A.
    Chiang, T.
    Seo, K.
    Arber, D. A.
    Zehnder, J.
    Schrijver, I.
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2009, 11 (06): : 627 - 627
  • [28] A Direct Sequencing Based Assay for Detection of CEBPA Mutations in Acute Myeloid Leukemia
    Betz, B. L.
    Weigelin, H. C.
    Johnson, K. S. Elenitoba
    JOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (06): : 870 - 871
  • [29] NANOPORE TARGET SEQUENCING FOR RAPID GENE MUTATIONS DETECTION IN ACUTE MYELOID LEUKEMIA
    Cumbo, C.
    Minervini, C. F.
    Orsini, P.
    Anelli, L.
    Zagaria, A.
    Minervini, A.
    Coccaro, N.
    Impera, L.
    Tota, G.
    Parciante, E.
    Conserva, M. R.
    Delia, M.
    Spinelli, O.
    Rambaldi, A.
    Specchia, G.
    Albano, F.
    HAEMATOLOGICA, 2019, 104 : 106 - 107
  • [30] IDH mutations in glioma and acute myeloid leukemia
    Dang, Lenny
    Jin, Shengfang
    Su, Shinsan M.
    TRENDS IN MOLECULAR MEDICINE, 2010, 16 (09) : 387 - 397