作者: Osamu Tomita , Kazutoshi Iijima , Takeshi Ishibashi , Tomoo Osumi , Kenichiro Kobayashi
DOI: 10.1016/J.LEUKRES.2013.11.017
关键词:
摘要: We introduced SNX2-ABL1, a novel ABL1-related chimeric transcript lacks SH3 and SH2 domains, into murine Ba/F3 cells compared their function with that of BCR-ABL1. After the expression SNX2-ABL1 proteins, acquired an ability to proliferate in IL-3-independent manner. Upon treatment both imatinib dasatinib, BCR-ABL1-expressing underwent rapid apoptosis, whereas SNX2-ABL1-expressing showed poorer sensitivity toward these TKIs could presence low dose dasatinib. Therefore, other more selective effect against this kinase should be used for patients SNX2-ABL1+ ALL.