z-logo
open-access-imgOpen Access
Prognostic Significance ofNOTCH1andFBXW7Mutations in Pediatric T-ALL
Author(s) -
Yücel Erbilgin,
Müge Sayitoğlu,
Özden Hatırnaz Ng,
Ömer Doğru,
Arzu Akçay,
Gülen Tüysüz,
Tıraje Celkan,
Gönül Aydoğan,
Zafer Şalcıoğlu,
Çetin Timur,
Lebriz Yüksel-Soycan,
Ümit Üre,
Sema Anak,
Leyla Ağaoğlu,
Ömer Devecioğlu,
İnci Yıldız,
Uğur Özbek
Publication year - 2010
Publication title -
disease markers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.912
H-Index - 66
eISSN - 1875-8630
pISSN - 0278-0240
DOI - 10.1155/2010/740140
Subject(s) - mutation , immunophenotyping , biology , t cell , lineage (genetic) , cancer research , genetics , gene , flow cytometry , immune system
The NOTCH signaling pathway plays important role in the development of multicellular organisms, as it regulates cell proliferation, survival, and differentiation. In adults, it is essential for the T- or B-lymphocyte lineage commitment. NOTCH1 and FBXW7 mutations both lead the activation of the NOTCH1 pathway and are found in the majority of T-ALL patients. In this study, the mutation analysis of NOTCH1 and FBXW7 genes was performed in 87 pediatric T-ALLs who were treated on the ALL-BFM protocols. In 19 patients (22%), activating NOTCH1 mutations were observed either in the heterodimerization domain or in the PEST domain and 7 cases (10%) demonstrated FBXW7 mutations (2 cases had both NOTCH1 and FBXW7 mutations). We also analyzed the relationship of the mutation data between the clinical and biological data of the patients. NOTCH1 and FBXW7 , NOTCH1 alone were found correlated with lower initial leucocyte counts which was independent from the sex and T- cell immunophenotype. However, NOTCH1 and FBXW7 mutations were not predictive of outcome in the overall cohort of pediatric T-ALLs.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom