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      Anaplastic lymphoma kinase: signalling in development and disease

      review-article
      1 , , , 1
      Biochemical Journal
      Portland Press Ltd.
      anaplastic lymphoma kinase (ALK), anaplastic large cell lymphoma (ALCL), extracellular-signal-regulated kinase (ERK), inflammatory myofibroblastic tumour (IMT), midkine, neuroblastoma, non-small cell lung cancer (NSLCL), pleiotrophin, ALCL, anaplastic large cell lymphoma, ALK, anaplastic lymphoma kinase, ALO17, ALK lymphoma oligomerization partner on chromosome 17, ATIC, 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase, BCR-Abl, breakpoint cluster region-Abl, CARS, cysteinyl-tRNA synthetase, Cdc42, cell division cycle 42, C/EBPβ, CCAAT/enhancer-binding protein β, CLTC, clathrin heavy chain, CML, chronic myeloid leukaemia, CNS, central nervous system, dALK, Drosophila ALK, DLBCL, diffuse large B-cell lymphoma, Dpp, decapentaplegic, DRG, dorsal root ganglia, EGFR, epidermal growth factor receptor, EML4, echinoderm microtubule-associated protein like 4, ERK, extracellular-signal-regulated kinase, FOXO3a, forkhead box O 3a, FRS2, fibroblast growth factor receptor substrate 2, GIST, gastrointestinal stromal tumour, Grb2, growthfactor-receptor-bound protein 2, HEK, human embryonic kidney, Hen-1, hesitation-1, IL-3, interleukin-3, IMT, inflammatory myofibroblastic tumour, IR, insulin receptor, IRS-1, IR substrate-1, JAK, Janus kinase, Jeb, jelly belly, JNK, c-Jun N-terminal kinase, LDLa, low-density lipoprotein class A, LTK, leucocyte tyrosine kinase, MAM, meprin, A5 protein and receptor protein tyrosine phosphatase mu, MAPK, mitogen-activated protein kinase, MEK, MAPK/ERK kinase, MK, midkine, MSN, moesin, mTOR, mammalian target of rapamycin, MUC-1, mucin-1, MYH9, non-muscle myosin heavy chain, NF-κB, nuclear factor κB, NIPA, nuclear interacting partner of ALK, NPM, nucleophosmin, NSCLC, non-small cell lung cancer, PI3K, phosphoinositide 3-kinase, PKB, protein kinase B, PLCγ, phospholipase Cγ, PTN, pleiotrophin, RANBP2, Ran-binding protein 2, RPTP, receptor protein tyrosine phosphatase, RTK, receptor tyrosine kinase, SCC, squamous cell carcinoma, SCD-2, suppressor of constitutive dauer 2, SEC31L1, SEC31 homologue A, SH2, Src homology 2, Shc, Src homology and collagen homology, SHH, sonic hedghog, Shp1, SH2 domain-containing phosphatase 1, STAT, signal transducer and activator of transcription, TFG, TRK-fused gene, TGFβ, transforming growth factor β, TPM, tropomyosin, UCN-01, unco-ordinated 1

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          Abstract

          RTKs (receptor tyrosine kinases) play important roles in cellular proliferation and differentiation. In addition, RTKs reveal oncogenic potential when their kinase activities are constitutively enhanced by point mutation, amplification or rearrangement of the corresponding genes. The ALK (anaplastic lymphoma kinase) RTK was originally identified as a member of the insulin receptor subfamily of RTKs that acquires transforming capability when truncated and fused to NPM (nucleophosmin) in the t(2;5) chromosomal rearrangement associated with ALCL (anaplastic large cell lymphoma). To date, many chromosomal rearrangements leading to enhanced ALK activity have been described and are implicated in a number of cancer types. Recent reports of the EML4 (echinoderm microtubule-associated protein like 4)–ALK oncoprotein in NSCLC (non-small cell lung cancer), together with the identification of activating point mutations in neuroblastoma, have highlighted ALK as a significant player and target for drug development in cancer. In the present review we address the role of ALK in development and disease and discuss implications for the future.

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          Most cited references219

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          Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer.

          Despite the success of tyrosine kinase-based cancer therapeutics, for most solid tumors the tyrosine kinases that drive disease remain unknown, limiting our ability to identify drug targets and predict response. Here we present the first large-scale survey of tyrosine kinase activity in lung cancer. Using a phosphoproteomic approach, we characterize tyrosine kinase signaling across 41 non-small cell lung cancer (NSCLC) cell lines and over 150 NSCLC tumors. Profiles of phosphotyrosine signaling are generated and analyzed to identify known oncogenic kinases such as EGFR and c-Met as well as novel ALK and ROS fusion proteins. Other activated tyrosine kinases such as PDGFRalpha and DDR1 not previously implicated in the genesis of NSCLC are also identified. By focusing on activated cell circuitry, the approach outlined here provides insight into cancer biology not available at the chromosomal and transcriptional levels and can be applied broadly across all human cancers.
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            Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells.

            The bcr-abl oncogene, present in 95% of patients with chronic myelogenous leukemia (CML), has been implicated as the cause of this disease. A compound, designed to inhibit the Abl protein tyrosine kinase, was evaluated for its effects on cells containing the Bcr-Abl fusion protein. Cellular proliferation and tumor formation by Bcr-Abl-expressing cells were specifically inhibited by this compound. In colony-forming assays of peripheral blood or bone marrow from patients with CML, there was a 92-98% decrease in the number of bcr-abl colonies formed but no inhibition of normal colony formation. This compound may be useful in the treatment of bcr-abl-positive leukemias.
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              Fusion of a kinase gene, ALK, to a nucleolar protein gene, NPM, in non-Hodgkin's lymphoma.

              The 2;5 chromosomal translocation occurs in most anaplastic large-cell non-Hodgkin's lymphomas arising from activated T lymphocytes. This rearrangement was shown to fuse the NPM nucleolar phosphoprotein gene on chromosome 5q35 to a previously unidentified protein tyrosine kinase gene, ALK, on chromosome 2p23. In the predicted hybrid protein, the amino terminus of nucleophosmin (NPM) is linked to the catalytic domain of anaplastic lymphoma kinase (ALK). Expressed in the small intestine, testis, and brain but not in normal lymphoid cells, ALK shows greatest sequence similarity to the insulin receptor subfamily of kinases. Unscheduled expression of the truncated ALK may contribute to malignant transformation in these lymphomas.
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                Author and article information

                Journal
                Biochem J
                bic
                BJ
                Biochemical Journal
                Portland Press Ltd.
                0264-6021
                1470-8728
                27 May 2009
                15 June 2009
                : 420
                : Pt 3
                : 345-361
                Affiliations
                Department of Molecular Biology, Building 6L, Umeå University, Umeå 901 87, Sweden
                Author notes
                1Correspondence may be addressed to either of these authors (email Ruth.Palmer@ 123456ucmp.umu.se or Bengt.Hallberg@ 123456molbiol.umu.se ).
                Article
                bj4200345
                10.1042/BJ20090387
                2708929
                19459784
                8da67b44-8909-4d2f-94a9-a10674538b38
                © 2009 The Author(s) The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 5 March 2009
                : 25 March 2009
                : 1 April 2009
                Page count
                Figures: 3, Tables: 2, References: 237, Pages: 17
                Categories
                Review Article

                Biochemistry
                dalk, drosophila alk,nipa, nuclear interacting partner of alk,neuroblastoma,dlbcl, diffuse large b-cell lymphoma,drg, dorsal root ganglia,tpm, tropomyosin,pi3k, phosphoinositide 3-kinase,myh9, non-muscle myosin heavy chain,irs-1, ir substrate-1,cltc, clathrin heavy chain,ranbp2, ran-binding protein 2,anaplastic large cell lymphoma (alcl),rtk, receptor tyrosine kinase,tgfβ, transforming growth factor β,imt, inflammatory myofibroblastic tumour,anaplastic lymphoma kinase (alk),erk, extracellular-signal-regulated kinase,rptp, receptor protein tyrosine phosphatase,non-small cell lung cancer (nslcl),il-3, interleukin-3,shh, sonic hedghog,pkb, protein kinase b,alk, anaplastic lymphoma kinase,sec31l1, sec31 homologue a,ptn, pleiotrophin,cns, central nervous system,mam, meprin, a5 protein and receptor protein tyrosine phosphatase mu,jak, janus kinase,ldla, low-density lipoprotein class a,cml, chronic myeloid leukaemia,midkine,gist, gastrointestinal stromal tumour,hen-1, hesitation-1,stat, signal transducer and activator of transcription,mk, midkine,scd-2, suppressor of constitutive dauer 2,alo17, alk lymphoma oligomerization partner on chromosome 17,plcγ, phospholipase cγ,mek, mapk/erk kinase,mapk, mitogen-activated protein kinase,bcr-abl, breakpoint cluster region-abl,egfr, epidermal growth factor receptor,extracellular-signal-regulated kinase (erk),jnk, c-jun n-terminal kinase,grb2, growthfactor-receptor-bound protein 2,nsclc, non-small cell lung cancer,sh2, src homology 2,alcl, anaplastic large cell lymphoma,cars, cysteinyl-trna synthetase,scc, squamous cell carcinoma,muc-1, mucin-1,pleiotrophin,frs2, fibroblast growth factor receptor substrate 2,atic, 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase,tfg, trk-fused gene,npm, nucleophosmin,hek, human embryonic kidney,jeb, jelly belly,inflammatory myofibroblastic tumour (imt),cdc42, cell division cycle 42,nf-κb, nuclear factor κb,shc, src homology and collagen homology,foxo3a, forkhead box o 3a,ucn-01, unco-ordinated 1,msn, moesin,shp1, sh2 domain-containing phosphatase 1,ltk, leucocyte tyrosine kinase,dpp, decapentaplegic,ir, insulin receptor,c/ebpβ, ccaat/enhancer-binding protein β,eml4, echinoderm microtubule-associated protein like 4,mtor, mammalian target of rapamycin
                Biochemistry
                dalk, drosophila alk, nipa, nuclear interacting partner of alk, neuroblastoma, dlbcl, diffuse large b-cell lymphoma, drg, dorsal root ganglia, tpm, tropomyosin, pi3k, phosphoinositide 3-kinase, myh9, non-muscle myosin heavy chain, irs-1, ir substrate-1, cltc, clathrin heavy chain, ranbp2, ran-binding protein 2, anaplastic large cell lymphoma (alcl), rtk, receptor tyrosine kinase, tgfβ, transforming growth factor β, imt, inflammatory myofibroblastic tumour, anaplastic lymphoma kinase (alk), erk, extracellular-signal-regulated kinase, rptp, receptor protein tyrosine phosphatase, non-small cell lung cancer (nslcl), il-3, interleukin-3, shh, sonic hedghog, pkb, protein kinase b, alk, anaplastic lymphoma kinase, sec31l1, sec31 homologue a, ptn, pleiotrophin, cns, central nervous system, mam, meprin, a5 protein and receptor protein tyrosine phosphatase mu, jak, janus kinase, ldla, low-density lipoprotein class a, cml, chronic myeloid leukaemia, midkine, gist, gastrointestinal stromal tumour, hen-1, hesitation-1, stat, signal transducer and activator of transcription, mk, midkine, scd-2, suppressor of constitutive dauer 2, alo17, alk lymphoma oligomerization partner on chromosome 17, plcγ, phospholipase cγ, mek, mapk/erk kinase, mapk, mitogen-activated protein kinase, bcr-abl, breakpoint cluster region-abl, egfr, epidermal growth factor receptor, extracellular-signal-regulated kinase (erk), jnk, c-jun n-terminal kinase, grb2, growthfactor-receptor-bound protein 2, nsclc, non-small cell lung cancer, sh2, src homology 2, alcl, anaplastic large cell lymphoma, cars, cysteinyl-trna synthetase, scc, squamous cell carcinoma, muc-1, mucin-1, pleiotrophin, frs2, fibroblast growth factor receptor substrate 2, atic, 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/imp cyclohydrolase, tfg, trk-fused gene, npm, nucleophosmin, hek, human embryonic kidney, jeb, jelly belly, inflammatory myofibroblastic tumour (imt), cdc42, cell division cycle 42, nf-κb, nuclear factor κb, shc, src homology and collagen homology, foxo3a, forkhead box o 3a, ucn-01, unco-ordinated 1, msn, moesin, shp1, sh2 domain-containing phosphatase 1, ltk, leucocyte tyrosine kinase, dpp, decapentaplegic, ir, insulin receptor, c/ebpβ, ccaat/enhancer-binding protein β, eml4, echinoderm microtubule-associated protein like 4, mtor, mammalian target of rapamycin

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