Alectinib, an Anaplastic Lymphoma Kinase Inhibitor, Abolishes ALK Activity and Growth in ALK-Positive Neuroblastoma Cells

被引:29
作者
Alam, Muhammad Wasi [1 ]
Borenas, Marcus [1 ]
Lind, Dan E. [1 ]
Cervantes-Madrid, Diana [1 ]
Umapathy, Ganesh [1 ]
Palmer, Ruth H. [1 ]
Hallberg, Bengt [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Dept Med Biochem & Cell Biol, Gothenburg, Sweden
来源
FRONTIERS IN ONCOLOGY | 2019年 / 9卷
基金
瑞典研究理事会;
关键词
neuroblastoma; alectinib; anaplastic lymphoma kinase (ALK); resistant mutations; xenograft; crizotinib; ALK inhibitors; RECEPTOR TYROSINE KINASE; LUNG-CANCER; ACTIVATING MUTATIONS; ANTITUMOR-ACTIVITY; TARGETING ALK; OPEN-LABEL; CRIZOTINIB; GENE; LIGANDS; PROTEIN;
D O I
10.3389/fonc.2019.00579
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Oncogenic receptor tyrosine kinases including anaplastic lymphoma kinase (ALK) are implicated in numerous solid and hematologic cancers. ALK mutations are reported in an estimated 9% of neuroblastoma and recent reports indicate that the percentage of ALK-positive cases increases in the relapsed patient population. Initial clinical trial results have shown that it is difficult to inhibit growth of ALK positive neuroblastoma with crizotinib, motivating investigation of next generation ALK inhibitors with higher affinity for ALK. Here, alectinib, a potent next generation ALK inhibitor with antitumor activity was investigated in ALK-driven neuroblastoma models. Employing neuroblastoma cell lines and mouse xenografts we show a clear and efficient inhibition of ALK activity by alectinib. Inhibition of ALK activity was observed in vitro employing a set of different constitutively active ALK variants in biochemical assays. The results suggest that alectinib is an effective inhibitor of ALK kinase activity in ALK addicted neuroblastoma and should be considered as a potential future therapeutic option for ALK-positive neuroblastoma patients alone or in combination with other treatments.
引用
收藏
页数:12
相关论文
共 60 条
  • [21] Mechanistic insight into ALK receptor tyrosine kinase in human cancer biology
    Hallberg, Bengt
    Palmer, Ruth H.
    [J]. NATURE REVIEWS CANCER, 2013, 13 (10) : 685 - 700
  • [22] Good clinical response to alectinib, a second generation ALK inhibitor, in refractory neuroblastoma
    Heath, John A.
    Campbell, Marty A.
    Thomas, Alison
    Solomon, Ben
    [J]. PEDIATRIC BLOOD & CANCER, 2018, 65 (07)
  • [23] Alectinib versus crizotinib in patients with ALK-positive non-small-cell lung cancer (J-ALEX): an open-label, randomised phase 3 trial
    Hida, Toyoaki
    Nokihara, Hiroshi
    Kondo, Masashi
    Kim, Young Hak
    Azuma, Koichi
    Seto, Takashi
    Takiguchi, Yuichi
    Nishio, Makoto
    Yoshioka, Hiroshige
    Imamura, Fumio
    Hotta, Katsuyuki
    Watanabe, Satoshi
    Goto, Koichi
    Satouchi, Miyako
    Kozuki, Toshiyuki
    Shukuya, Takehito
    Nakagawa, Kazuhiko
    Mitsudomi, Tetsuya
    Yamamoto, Nobuyuki
    Asakawa, Takashi
    Asabe, Ryoichi
    Tanaka, Tomohiro
    Tamura, Tomohide
    [J]. LANCET, 2017, 390 (10089) : 29 - 39
  • [24] Molecular characterization of ALK, a receptor tyrosine kinase expressed specifically in the nervous system
    Iwahara, T
    Fujimoto, J
    Wen, DZ
    Cupples, R
    Bucay, N
    Arakawa, T
    Mori, S
    Ratzkin, B
    Yamamoto, T
    [J]. ONCOGENE, 1997, 14 (04) : 439 - 449
  • [25] Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
    Janoueix-Lerosey, Isabelle
    Lequin, Delphine
    Brugieres, Laurence
    Ribeiro, Agnes
    de Pontual, Loic
    Combaret, Valerie
    Raynal, Virginie
    Puisieux, Alain
    Schleiermacher, Gudrun
    Pierron, Gaelle
    Valteau-Couanet, Dominique
    Frebourg, Thierry
    Michon, Jean
    Lyonnet, Stanislas
    Amiel, Jeanne
    Delattre, Olivier
    [J]. NATURE, 2008, 455 (7215) : 967 - U51
  • [26] Design and synthesis of a highly selective, orally active and potent anaplastic lymphoma kinase inhibitor (CH5424802)
    Kinoshita, Kazutomo
    Asoh, Kohsuke
    Furuichi, Noriyuki
    Ito, Toshiya
    Kawada, Hatsuo
    Hara, Sousuke
    Ohwada, Jun
    Miyagi, Takuho
    Kobayashi, Takamitsu
    Takanashi, Kenji
    Tsukaguchi, Toshiyuki
    Sakamoto, Hiroshi
    Tsukuda, Takuo
    Oikawa, Nobuhiro
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (03) : 1271 - 1280
  • [27] Selective ALK inhibitor alectinib with potent antitumor activity in models of crizotinib resistance
    Kodama, Tatsushi
    Tsukaguchi, Toshiyuki
    Yoshida, Miyuki
    Kondoh, Osamu
    Sakamoto, Hiroshi
    [J]. CANCER LETTERS, 2014, 351 (02) : 215 - 221
  • [28] Dynamics-Driven Allostery in Protein Kinases
    Kornev, Alexandr P.
    Taylor, Susan S.
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2015, 40 (11) : 628 - 647
  • [29] Defining the conserved internal architecture of a protein kinase
    Kornev, Alexandr P.
    Taylor, Susan S.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2010, 1804 (03): : 440 - 444
  • [30] Anaplastic Lymphoma Kinase Inhibition in Non-Small-Cell Lung Cancer
    Kwak, Eunice L.
    Bang, Yung-Jue
    Camidge, D. Ross
    Shaw, Alice T.
    Solomon, Benjamin
    Maki, Robert G.
    Ou, Sai-Hong I.
    Dezube, Bruce J.
    Jaenne, Pasi A.
    Costa, Daniel B.
    Varella-Garcia, Marileila
    Kim, Woo-Ho
    Lynch, Thomas J.
    Fidias, Panos
    Stubbs, Hannah
    Engelman, Jeffrey A.
    Sequist, Lecia V.
    Tan, WeiWei
    Gandhi, Leena
    Mino-Kenudson, Mari
    Wei, Greg C.
    Shreeve, S. Martin
    Ratain, Mark J.
    Settleman, Jeffrey
    Christensen, James G.
    Haber, Daniel A.
    Wilner, Keith
    Salgia, Ravi
    Shapiro, Geoffrey I.
    Clark, Jeffrey W.
    Iafrate, A. John
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2010, 363 (18) : 1693 - 1703