Eadie Laura N, Hughes Timothy P, White Deborah L
Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, South Australia.
Department of Medicine, University of Adelaide, Adelaide, South Australia.
PLoS One. 2016 Aug 18;11(8):e0161470. doi: 10.1371/journal.pone.0161470. eCollection 2016.
The tyrosine kinase inhibitor (TKI) imatinib has resulted in excellent responses in the majority of Chronic Myeloid Leukaemia (CML) patients; however, resistance is observed in 20-30% of patients. More recently, resistance to the second generation TKIs, nilotinib and dasatinib, has also been observed albeit at a lower incidence. ABCB1 has previously been implicated in TKI export and its overexpression linked to TKI resistance. In this study the dynamics of nilotinib resistance was studied in CML cell lines with particular focus on ABCB1 expression levels during development of resistance. Results revealed ABCB1 overexpression is likely an important initiator of nilotinib resistance in vitro. ABCB1 overexpression was also observed in cell lines as an intermediate step during development of resistance to imatinib and dasatinib in vitro. We conclude that ABCB1 overexpression may provide an initial platform to facilitate development of additional mechanisms for resistance to TKIs. This provides a rationale for investigating this phenomenon in patients undergoing TKI therapy.
酪氨酸激酶抑制剂(TKI)伊马替尼已使大多数慢性髓性白血病(CML)患者产生良好疗效;然而,20%-30%的患者会出现耐药。最近,第二代TKI尼洛替尼和达沙替尼也出现了耐药情况,尽管发生率较低。ABCB1此前被认为与TKI的外排有关,其过表达与TKI耐药相关。在本研究中,对CML细胞系中尼洛替尼耐药的动态变化进行了研究,特别关注耐药发展过程中ABCB1的表达水平。结果显示,ABCB1过表达可能是体外尼洛替尼耐药的重要起始因素。在体外对伊马替尼和达沙替尼耐药发展的中间阶段,细胞系中也观察到ABCB1过表达。我们得出结论,ABCB1过表达可能提供一个初始平台,以促进对TKI产生额外耐药机制的发展。这为在接受TKI治疗的患者中研究这一现象提供了理论依据。