메뉴 건너뛰기




Volumn 5, Issue 1, 2015, Pages 34-37

Alectinib: A novel second generation anaplastic lymphoma kinase (ALK) inhibitor for overcoming clinically-acquired resistance

Author keywords

Alectinib; ALK mutations; Crizotinib; EML4 ALK; Non small cell lung cancer; Resistance; Tyrosine anaplastic lymphoma kinase

Indexed keywords

ALECTINIB; ANAPLASTIC LYMPHOMA KINASE; CRIZOTINIB;

EID: 84945189935     PISSN: 22113835     EISSN: 22113843     Source Type: Journal    
DOI: 10.1016/j.apsb.2014.12.007     Document Type: Review
Times cited : (72)

References (21)
  • 1
    • 0028198206 scopus 로고
    • Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin[U+05F3]s lymphoma
    • Morris S.W., Kirstein M.N., Valentine M.B., Dittmer K.G., Shapiro D.N., Saltman D.L., et al. Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin[U+05F3]s lymphoma. Science 1994, 263:1281-1284.
    • (1994) Science , vol.263 , pp. 1281-1284
    • Morris, S.W.1    Kirstein, M.N.2    Valentine, M.B.3    Dittmer, K.G.4    Shapiro, D.N.5    Saltman, D.L.6
  • 2
    • 36849065315 scopus 로고    scopus 로고
    • Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer
    • Rikova K., Guo A.L., Zeng Q.F., Possemato A., Yu J., Haack H., et al. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Cell 2007, 131:1190-1203.
    • (2007) Cell , vol.131 , pp. 1190-1203
    • Rikova, K.1    Guo, A.L.2    Zeng, Q.F.3    Possemato, A.4    Yu, J.5    Haack, H.6
  • 3
    • 34547638047 scopus 로고    scopus 로고
    • Identification of the transforming EML4-ALK fusion gene in non-small-cell lung cancer
    • Soda M., Choi Y.L., 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, 448:561-566.
    • (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
  • 4
    • 84872288990 scopus 로고    scopus 로고
    • Anaplastic lymphoma kinase (ALK): structure, oncogenic activation, and pharmacological inhibition
    • Roskoski R. Anaplastic lymphoma kinase (ALK): structure, oncogenic activation, and pharmacological inhibition. Pharmacol Res 2013, 68:68-94.
    • (2013) Pharmacol Res , vol.68 , pp. 68-94
    • Roskoski, R.1
  • 5
    • 79954606778 scopus 로고    scopus 로고
    • Targeting anaplastic lymphoma kinase in lung cancer
    • Shaw A.T., Solomon B. Targeting anaplastic lymphoma kinase in lung cancer. Clin Cancer Res 2011, 17:2081-2086.
    • (2011) Clin Cancer Res , vol.17 , pp. 2081-2086
    • Shaw, A.T.1    Solomon, B.2
  • 7
    • 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 J.J., Tran-Dubé M., Shen H., Nambu M., Kung P.P., 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 2011, 54:6342-6363.
    • (2011) J Med Chem , vol.54 , pp. 6342-6363
    • Cui, J.J.1    Tran-Dubé, M.2    Shen, H.3    Nambu, M.4    Kung, P.P.5    Pairish, M.6
  • 8
    • 84884158867 scopus 로고    scopus 로고
    • Case history: Xalkori™ (crizotinib), a potent and selective dual inhibitor of mesenchymal epithelial transition (MET) and anaplastic lymphoma kinase (ALK) for cancer treatment
    • Cui J.J., McTigue M., Kania R., Edwards M.P. Case history: Xalkori™ (crizotinib), a potent and selective dual inhibitor of mesenchymal epithelial transition (MET) and anaplastic lymphoma kinase (ALK) for cancer treatment. Ann Rep Med Chem 2013, 48:421-432.
    • (2013) Ann Rep Med Chem , vol.48 , pp. 421-432
    • Cui, J.J.1    McTigue, M.2    Kania, R.3    Edwards, M.P.4
  • 9
    • 80053386829 scopus 로고    scopus 로고
    • Effect of crizotinib on overall survival in patients with advanced non-small-cell lung cancer harbouring ALK gene rearrangement: a retrospective analysis
    • Shaw A.T., Yeap B.Y., Solomon B.J., Riely G.J., Gainor J., Engelman J.A., et al. Effect of crizotinib on overall survival in patients with advanced non-small-cell lung cancer harbouring ALK gene rearrangement: a retrospective analysis. Lancet Oncol 2011, 12:1004-1012.
    • (2011) Lancet Oncol , vol.12 , pp. 1004-1012
    • Shaw, A.T.1    Yeap, B.Y.2    Solomon, B.J.3    Riely, G.J.4    Gainor, J.5    Engelman, J.A.6
  • 10
    • 84856990335 scopus 로고    scopus 로고
    • Mechanisms of resistance to crizotinib in patients with ALK gene rearranged non-small cell lung cancer
    • Doebele R.C., Pilling A.B., Aisner D.L., Kutateladze T.G., Le A.T., Weickhardt A.J., et al. Mechanisms of resistance to crizotinib in patients with ALK gene rearranged non-small cell lung cancer. Clin Cancer Res 2012, 18:1472-1482.
    • (2012) Clin Cancer Res , vol.18 , pp. 1472-1482
    • Doebele, R.C.1    Pilling, A.B.2    Aisner, D.L.3    Kutateladze, T.G.4    Le, A.T.5    Weickhardt, A.J.6
  • 11
    • 84866748344 scopus 로고    scopus 로고
    • Anaplastic lymphoma kinase inhibitors for the treatment of ALK-positive cancers
    • Kinoshita K., Oikawa N., Tsukuda T. Anaplastic lymphoma kinase inhibitors for the treatment of ALK-positive cancers. Ann Rep Med Chem 2012, 47:281-293.
    • (2012) Ann Rep Med Chem , vol.47 , pp. 281-293
    • Kinoshita, K.1    Oikawa, N.2    Tsukuda, T.3
  • 12
    • 78049426513 scopus 로고    scopus 로고
    • EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors
    • Choi Y.L., Soda M., Yamashita Y., Ueno T., Takashima J., Nakajima T., et al. EML4-ALK mutations in lung cancer that confer resistance to ALK inhibitors. N Engl J Med 2010, 363:1734-1739.
    • (2010) N Engl J Med , vol.363 , pp. 1734-1739
    • Choi, Y.L.1    Soda, M.2    Yamashita, Y.3    Ueno, T.4    Takashima, J.5    Nakajima, T.6
  • 13
    • 84904035862 scopus 로고    scopus 로고
    • Second generation ALK inhibitors: filling the non 'MET' gap
    • Ramalingam S., Khuri F.P. Second generation ALK inhibitors: filling the non 'MET' gap. Cancer Disc 2014, 4:634-636.
    • (2014) Cancer Disc , vol.4 , pp. 634-636
    • Ramalingam, S.1    Khuri, F.P.2
  • 14
    • 84906534354 scopus 로고    scopus 로고
    • Anaplastic lymphoma kinase (ALK) inhibitors: a review of design and discovery
    • Wang W.C., Shiao H.Y., Lee C.C., Fung K.S., Hsieh H.P. Anaplastic lymphoma kinase (ALK) inhibitors: a review of design and discovery. Med Chem Commun 2014, 5:1266-1279.
    • (2014) Med Chem Commun , vol.5 , pp. 1266-1279
    • Wang, W.C.1    Shiao, H.Y.2    Lee, C.C.3    Fung, K.S.4    Hsieh, H.P.5
  • 15
    • 84905190188 scopus 로고    scopus 로고
    • ALK inhibitors in non-small cell lung cancer: crizotinib and beyond
    • Awad M.M., Shaw A.T. ALK inhibitors in non-small cell lung cancer: crizotinib and beyond. Clin Adv Hematol Oncol 2014, 12:429-439.
    • (2014) Clin Adv Hematol Oncol , vol.12 , pp. 429-439
    • Awad, M.M.1    Shaw, A.T.2
  • 16
    • 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-(isopropylsulfonyl)phenyl)pyrimidine-2, 4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials
    • Marsilje T.H., 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-(isopropylsulfonyl)phenyl)pyrimidine-2, 4-diamine (LDK378) currently in phase 1 and phase 2 clinical trials. J Med Chem 2013, 56:5675-5690.
    • (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
  • 18
    • 84884203754 scopus 로고    scopus 로고
    • Journey of the ALK-inhibitor CH5424802 to phase II clinical trial
    • Latif M., Saeed A., Kim S.H. Journey of the ALK-inhibitor CH5424802 to phase II clinical trial. Arch Pharm Res 2013, 36:1051-1054.
    • (2013) Arch Pharm Res , vol.36 , pp. 1051-1054
    • Latif, M.1    Saeed, A.2    Kim, S.H.3
  • 19
    • 80052791063 scopus 로고    scopus 로고
    • 9-Substituted 6, 6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazoles as highly selective and potent anaplastic lymphoma kinase inhibitors
    • Kinoshita K., Kobayashi T., Asoh K., Furuichi N., Ito T., Kawada H., et al. 9-Substituted 6, 6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazoles as highly selective and potent anaplastic lymphoma kinase inhibitors. J Med Chem 2011, 54:6286-6294.
    • (2011) J Med Chem , vol.54 , pp. 6286-6294
    • Kinoshita, K.1    Kobayashi, T.2    Asoh, K.3    Furuichi, N.4    Ito, T.5    Kawada, H.6
  • 20
    • 79955964568 scopus 로고    scopus 로고
    • CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant
    • Sakamoto H., Tsukaguchi T., Hiroshima S., Kodama T., Kobayashi T., Fukami T.A., et al. CH5424802, a selective ALK inhibitor capable of blocking the resistant gatekeeper mutant. Cancer Cell 2011, 19:679-690.
    • (2011) Cancer Cell , vol.19 , pp. 679-690
    • Sakamoto, H.1    Tsukaguchi, T.2    Hiroshima, S.3    Kodama, T.4    Kobayashi, T.5    Fukami, T.A.6
  • 21
    • 84878347085 scopus 로고    scopus 로고
    • CH5424802 (RO5424802) for patients with ALK-rearranged advanced non-small-cell lung cancer (AF-001JP study): a single-arm, open-label, phase 1-2 study
    • Seto T., Kiura K., Nishio M., Nakagawa K., Maemondo M., Inoue A., et al. CH5424802 (RO5424802) for patients with ALK-rearranged advanced non-small-cell lung cancer (AF-001JP study): a single-arm, open-label, phase 1-2 study. Lancet Oncol 2013, 14:590-598.
    • (2013) Lancet Oncol , vol.14 , pp. 590-598
    • Seto, T.1    Kiura, K.2    Nishio, M.3    Nakagawa, K.4    Maemondo, M.5    Inoue, A.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.