메뉴 건너뛰기




Volumn 4, Issue 6, 2014, Pages 662-673

The ALK inhibitor ceritinib overcomes crizotinib resistance in non-small cell lung cancer

(24)  Friboulet, Luc a,b   Li, Nanxin c   Katayama, Ryohei a,b,d   Lee, Christian C c   Gainor, Justin F a,b   Crystal, Adam S a,b   Michellys, Pierre Yves c   Awad, Mark M a,b   Yanagitani, Noriko e   Kim, Sungjoon c   Pferdekamper, Anne Marie C a   Li, Jie c   Kasibhatla, Shailaja c   Sun, Frank c   Sun, Xiuying c   Hua, Su c   McNamara, Peter c   Mahmood, Sidra a,b   Lockerman, Elizabeth L a,b   Fujita, Naoya d   more..


Author keywords

[No Author keywords available]

Indexed keywords

ANAPLASTIC LYMPHOMA KINASE; CERITINIB; CRIZOTINIB; MAMMALIAN TARGET OF RAPAMYCIN; MITOGEN ACTIVATED PROTEIN KINASE; MITOGEN ACTIVATED PROTEIN KINASE KINASE; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; ANTINEOPLASTIC AGENT; PROTEIN KINASE INHIBITOR; PROTEIN TYROSINE KINASE; PYRAZOLE DERIVATIVE; PYRIDINE DERIVATIVE; PYRIMIDINE DERIVATIVE; SULFONE;

EID: 84903466222     PISSN: 21598274     EISSN: 21598290     Source Type: Journal    
DOI: 10.1158/2159-8290.CD-13-0846     Document Type: Article
Times cited : (721)

References (19)
  • 2
    • 34547638047 scopus 로고    scopus 로고
    • Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
    • Soda M, Choi YL, Enomoto M, Takada S, Yamashita Y, Ishikawa S, et al. Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer. Nature 2007; 448: 561-6.
    • (2007) Nature , vol.448 , pp. 561-566
    • Soda, M.1    Choi, Y.L.2    Enomoto, M.3    Takada, S.4    Yamashita, Y.5    Ishikawa, S.6
  • 5
    • 84881256393 scopus 로고    scopus 로고
    • ALK rearrangements are mutually exclusive with mutations in EGFR or KRAS: An analysis of 1,683 patients with non-small cell lung cancer
    • Gainor JF, Varghese AM, Ou SH, Kabraji S, Awad MM, Katayama R, et al. ALK rearrangements are mutually exclusive with mutations in EGFR or KRAS: an analysis of 1,683 patients with non-small cell lung cancer. Clin Cancer Res 2013; 19: 4273-81.
    • (2013) Clin Cancer Res , vol.19 , pp. 4273-4281
    • Gainor, J.F.1    Varghese, A.M.2    Ou, S.H.3    Kabraji, S.4    Awad, M.M.5    Katayama, R.6
  • 7
  • 8
    • 84857027931 scopus 로고    scopus 로고
    • Escaping ALK inhibition: Mechanisms of and strategies to overcome resistance
    • Lovly CM, Pao W. Escaping ALK inhibition: mechanisms of and strategies to overcome resistance. Sci Transl Med 2012; 4: 120ps122.
    • (2012) Sci Transl Med , vol.4
    • Lovly, C.M.1    Pao, W.2
  • 9
    • 80052793410 scopus 로고    scopus 로고
    • A novel ALK secondary mutation and EGFR signaling cause resistance to ALK kinase inhibitors
    • Sasaki T, Koivunen J, Ogino A, Yanagita M, Nikiforow S, Zheng W, et al. A novel ALK secondary mutation and EGFR signaling cause resistance to ALK kinase inhibitors. Cancer Res 2011; 71: 6051-60.
    • (2011) Cancer Res , vol.71 , pp. 6051-6060
    • Sasaki, T.1    Koivunen, J.2    Ogino, A.3    Yanagita, M.4    Nikiforow, S.5    Zheng, W.6
  • 10
    • 78649475696 scopus 로고    scopus 로고
    • The neuroblastoma-associated F1174L ALK mutation causes resistance to an ALK kinase inhibitor in ALK-translocated cancers
    • Sasaki T, Okuda K, Zheng W, Butrynski J, Capelletti M, Wang L, et al. The neuroblastoma-associated F1174L ALK mutation causes resistance to an ALK kinase inhibitor in ALK-translocated cancers. Cancer Res 2010; 70: 10038-43.
    • (2010) Cancer Res , vol.70 , pp. 10038-10043
    • Sasaki, T.1    Okuda, K.2    Zheng, W.3    Butrynski, J.4    Capelletti, M.5    Wang, L.6
  • 11
    • 79956318797 scopus 로고    scopus 로고
    • Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK
    • Katayama R, Khan TM, Benes C, Lifshits E, Ebi H, Rivera VM, et al. Therapeutic strategies to overcome crizotinib resistance in non-small cell lung cancers harboring the fusion oncogene EML4-ALK. Proc Natl Acad Sci U S A 2011; 108: 7535-40.
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 7535-7540
    • Katayama, R.1    Khan, T.M.2    Benes, C.3    Lifshits, E.4    Ebi, H.5    Rivera, V.M.6
  • 12
    • 84880877176 scopus 로고    scopus 로고
    • Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-Chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulf onyl)phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials
    • Marsilje TH, Pei W, Chen B, Lu W, Uno T, Jin Y, et al. Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-Chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulf onyl)phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials. J Med Chem 2013; 56: 5675-90.
    • (2013) J Med Chem , vol.56 , pp. 5675-5690
    • Marsilje, T.H.1    Pei, W.2    Chen, B.3    Lu, W.4    Uno, T.5    Jin, Y.6
  • 14
    • 84881506681 scopus 로고    scopus 로고
    • Early Results Promising for LKD378 in ALK-positive NSCLC
    • OF5
    • Early Results Promising for LKD378 in ALK-positive NSCLC. Cancer Discov 2013; 3: OF5.
    • (2013) Cancer Discov , vol.3
  • 15
    • 0012164128 scopus 로고    scopus 로고
    • Application Number: 202570Orig1s000; Reference ID: 3006911
    • FDA, Center for Drug Evaluation and Research. 2011 Application Number: 202570Orig1s000; Reference ID: 3006911.
    • (2011) FDA, Center for Drug Evaluation and Research.
  • 16
    • 80052806086 scopus 로고    scopus 로고
    • Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK)
    • Cui JJ, Tran-Dube M, Shen H, Nambu M, Kung PP, Pairish M, et al. Structure based drug design of crizotinib (PF-02341066), a potent and selective dual inhibitor of mesenchymal-epithelial transition factor (c-MET) kinase and anaplastic lymphoma kinase (ALK). J Med Chem 2010; 54: 6342-63.
    • (2010) J Med Chem , vol.54 , pp. 6342-6363
    • Cui, J.J.1    Tran-Dube, M.2    Shen, H.3    Nambu, M.4    Kung, P.P.5    Pairish, M.6
  • 17
    • 84875157529 scopus 로고    scopus 로고
    • Cell culture and Drosophila model systems define three classes of anaplastic lymphoma kinase mutations in neuroblastoma
    • Chand D, Yamazaki Y, Ruuth K, Schonherr C, Martinsson T, Kogner P, et al. Cell culture and Drosophila model systems define three classes of anaplastic lymphoma kinase mutations in neuroblastoma. Dis Models & Mech 2013; 6: 373-82.
    • (2013) Dis Models & Mech , vol.6 , pp. 373-382
    • Chand, D.1    Yamazaki, Y.2    Ruuth, K.3    Schonherr, C.4    Martinsson, T.5    Kogner, P.6
  • 18
    • 77956691818 scopus 로고    scopus 로고
    • Crystal structure of the ALK (anaplastic lymphoma kinase) catalytic domain
    • Lee CC, Jia Y, Li N, Sun X, Ng K, Ambing E, et al. Crystal structure of the ALK (anaplastic lymphoma kinase) catalytic domain. Biochem J 2010; 430: 425-37.
    • (2010) Biochem J , vol.430 , pp. 425-437
    • Lee, C.C.1    Jia, Y.2    Li, N.3    Sun, X.4    Ng, K.5    Ambing, E.6
  • 19
    • 81355124049 scopus 로고    scopus 로고
    • Crizotinib-resistant mutants of EML4-ALK identified through an accelerated mutagenesis screen
    • Zhang S, Wang F, Keats J, Zhu X, Ning Y, Wardwell SD, et al. Crizotinib-resistant mutants of EML4-ALK identified through an accelerated mutagenesis screen. Chem Biol Drug Des 2011; 78: 999-1005.
    • (2011) Chem Biol Drug Des , vol.78 , pp. 999-1005
    • Zhang, S.1    Wang, F.2    Keats, J.3    Zhu, X.4    Ning, Y.5    Wardwell, S.D.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.