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Volumn 202, Issue 2, 2010, Pages 94-100

CLCA2, a novel RUNX1 partner gene in a therapy-related leukemia with t(1;21)(p22;q22)

Author keywords

[No Author keywords available]

Indexed keywords

BUSULFAN; CALCIUM ACTIVATED CHLORIDE CHANNEL; CHLORIDE CHANNEL; CYTARABINE; FLUDARABINE; IDARUBICIN; ISOPROTEIN; TRANSCRIPTION FACTOR RUNX1; UNCLASSIFIED DRUG; CLCA2 PROTEIN, HUMAN;

EID: 77957049320     PISSN: 01654608     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cancergencyto.2010.07.116     Document Type: Article
Times cited : (8)

References (31)
  • 1
    • 0035834962 scopus 로고    scopus 로고
    • Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1
    • Levanon D., Glusman G., Bangsow T., Ben-Asher E., Male D.A., Avidan N., et al. Architecture and anatomy of the genomic locus encoding the human leukemia-associated transcription factor RUNX1/AML1. Gene 2001, 262:23-33.
    • (2001) Gene , vol.262 , pp. 23-33
    • Levanon, D.1    Glusman, G.2    Bangsow, T.3    Ben-Asher, E.4    Male, D.A.5    Avidan, N.6
  • 3
    • 33645964017 scopus 로고    scopus 로고
    • Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique Hematologique
    • Jeandidier E., Dastugue N., Mugneret F., Lafage-Pochitaloff M., Mozziconacci M.J., Herens C., et al. Abnormalities of the long arm of chromosome 21 in 107 patients with hematopoietic disorders: a collaborative retrospective study of the Groupe Francais de Cytogenetique Hematologique. Cancer Genet Cytogenet 2006, 166:1-11.
    • (2006) Cancer Genet Cytogenet , vol.166 , pp. 1-11
    • Jeandidier, E.1    Dastugue, N.2    Mugneret, F.3    Lafage-Pochitaloff, M.4    Mozziconacci, M.J.5    Herens, C.6
  • 4
    • 33744502344 scopus 로고    scopus 로고
    • Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML
    • Stevens-Kroef M.J., Schoenmakers E.F., van Kraaij M., Huys E., Vermeulen S., van der Reijden B., et al. Identification of truncated RUNX1 and RUNX1-PRDM16 fusion transcripts in a case of t(1;21)(p36;q22)-positive therapy-related AML. Leukemia 2006, 20:1187-1189.
    • (2006) Leukemia , vol.20 , pp. 1187-1189
    • Stevens-Kroef, M.J.1    Schoenmakers, E.F.2    van Kraaij, M.3    Huys, E.4    Vermeulen, S.5    van der Reijden, B.6
  • 5
    • 0043028654 scopus 로고    scopus 로고
    • Fusion of AML1/Runx1 to copine VIII, a novel member of the copine family, in an aggressive acute myelogenous leukemia with t(12;21) translocation
    • Ramsey H., Zhang D.E., Richkind K., Burcoglu-O'Ral A., Hromas R. Fusion of AML1/Runx1 to copine VIII, a novel member of the copine family, in an aggressive acute myelogenous leukemia with t(12;21) translocation. Leukemia 2003, 17:1665-1666.
    • (2003) Leukemia , vol.17 , pp. 1665-1666
    • Ramsey, H.1    Zhang, D.E.2    Richkind, K.3    Burcoglu-O'Ral, A.4    Hromas, R.5
  • 6
    • 0347357871 scopus 로고    scopus 로고
    • A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia
    • Mikhail F.M., Coignet L., Hatem N., Mourad Z.I., Farawela H.M., et al. A novel gene, FGA7, is fused to RUNX1/AML1 in a t(4;21)(q28;q22) in a patient with T-cell acute lymphoblastic leukemia. Genes Chromosomes Cancer 2004, 39:110-118.
    • (2004) Genes Chromosomes Cancer , vol.39 , pp. 110-118
    • Mikhail, F.M.1    Coignet, L.2    Hatem, N.3    Mourad, Z.I.4    Farawela, H.M.5
  • 7
    • 0035313386 scopus 로고    scopus 로고
    • Fusion AML1 transcript in a radiation-associated leukemia results in a truncated inhibitory AML1 protein
    • Hromas R., Busse T., Carroll A., Mack D., Shopnick R., Zhang D.E., et al. Fusion AML1 transcript in a radiation-associated leukemia results in a truncated inhibitory AML1 protein. Blood 2001, 97:2168-2170.
    • (2001) Blood , vol.97 , pp. 2168-2170
    • Hromas, R.1    Busse, T.2    Carroll, A.3    Mack, D.4    Shopnick, R.5    Zhang, D.E.6
  • 8
    • 50049102936 scopus 로고    scopus 로고
    • Identification and characterization of novel AML1-ETO fusion transcripts in pediatric t(8;21) acute myeloid leukemia: a report from the Children's Oncology Group
    • LaFiura K.M., Edwards H., Taub J.W., Matherly L.H., Fontana J.A., Mohamed A.N., et al. Identification and characterization of novel AML1-ETO fusion transcripts in pediatric t(8;21) acute myeloid leukemia: a report from the Children's Oncology Group. Oncogene 2008, 27:4933-4942.
    • (2008) Oncogene , vol.27 , pp. 4933-4942
    • LaFiura, K.M.1    Edwards, H.2    Taub, J.W.3    Matherly, L.H.4    Fontana, J.A.5    Mohamed, A.N.6
  • 9
    • 0030053576 scopus 로고    scopus 로고
    • Rearrangement of the AML1/CBFA2 gene in myeloid leukemia with the 3;21 translocation: expression of co-existing multiple chimeric genes with similar functions as transcriptional repressors, but with opposite tumorigenic properties
    • Zent C., Kim N., Hiebert S., Zhang D.E., Tenen D.G., Rowley J.D., et al. Rearrangement of the AML1/CBFA2 gene in myeloid leukemia with the 3;21 translocation: expression of co-existing multiple chimeric genes with similar functions as transcriptional repressors, but with opposite tumorigenic properties. Curr Top Microbiol Immunol 1996, 211:243-252.
    • (1996) Curr Top Microbiol Immunol , vol.211 , pp. 243-252
    • Zent, C.1    Kim, N.2    Hiebert, S.3    Zhang, D.E.4    Tenen, D.G.5    Rowley, J.D.6
  • 10
    • 70350220616 scopus 로고    scopus 로고
    • LPXN, a member of the paxillin superfamily, is fused to RUNX1 in an acute myeloid leukemia patient with a t(11;21)(q12;q22) translocation
    • Dai H.P., Xue Y.Q., Zhou J.W., Li A.P., Wu Y.F., Pan J.L., et al. LPXN, a member of the paxillin superfamily, is fused to RUNX1 in an acute myeloid leukemia patient with a t(11;21)(q12;q22) translocation. Genes Chromosomes Cancer 2009, 48:1027-1036.
    • (2009) Genes Chromosomes Cancer , vol.48 , pp. 1027-1036
    • Dai, H.P.1    Xue, Y.Q.2    Zhou, J.W.3    Li, A.P.4    Wu, Y.F.5    Pan, J.L.6
  • 11
    • 38149102419 scopus 로고    scopus 로고
    • RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation
    • Nadal N., Stephan J.L., Cornillon J., Guyotat D., Flandrin P., Campos L. RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation. Cancer Genet Cytogenet 2008, 180:168-169.
    • (2008) Cancer Genet Cytogenet , vol.180 , pp. 168-169
    • Nadal, N.1    Stephan, J.L.2    Cornillon, J.3    Guyotat, D.4    Flandrin, P.5    Campos, L.6
  • 13
    • 0032996624 scopus 로고    scopus 로고
    • Molecular cloning and transmembrane structure of hCLCA2 from human lung, trachea, and mammary gland
    • Gruber A.D., Schreur K.D., Ji H.L., Fuller C.M., Pauli B.U. Molecular cloning and transmembrane structure of hCLCA2 from human lung, trachea, and mammary gland. Am J Physiol 1999, 276:C1261-C1270.
    • (1999) Am J Physiol , vol.276
    • Gruber, A.D.1    Schreur, K.D.2    Ji, H.L.3    Fuller, C.M.4    Pauli, B.U.5
  • 14
    • 0033231071 scopus 로고    scopus 로고
    • 2+-activated chloride channel CLCA2
    • 2+-activated chloride channel CLCA2. Cancer Res 1999, 59:5488-5491.
    • (1999) Cancer Res , vol.59 , pp. 5488-5491
    • Gruber, A.D.1    Pauli, B.U.2
  • 15
    • 40049110403 scopus 로고    scopus 로고
    • 5′RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia
    • Stavropoulou C., Georgakakos V.N., Manola K.N., Pagoni M., Garofalaki M., Pantelias G.E., et al. 5′RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia. Cancer Genet Cytogenet 2008, 182:50-55.
    • (2008) Cancer Genet Cytogenet , vol.182 , pp. 50-55
    • Stavropoulou, C.1    Georgakakos, V.N.2    Manola, K.N.3    Pagoni, M.4    Garofalaki, M.5    Pantelias, G.E.6
  • 16
    • 0035383839 scopus 로고    scopus 로고
    • Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis
    • Kolomietz E., Al-Maghrabi J., Brennan S., Karaskova J., Minkin S., Lipton J., et al. Primary chromosomal rearrangements of leukemia are frequently accompanied by extensive submicroscopic deletions and may lead to altered prognosis. Blood 2001, 97:3581-3588.
    • (2001) Blood , vol.97 , pp. 3581-3588
    • Kolomietz, E.1    Al-Maghrabi, J.2    Brennan, S.3    Karaskova, J.4    Minkin, S.5    Lipton, J.6
  • 17
    • 0030034804 scopus 로고    scopus 로고
    • The chimeric genes AML1/MDS1 and AML1/EAP inhibit AML1B activation at the CSF1R promoter, but only AML1/MDS1 has tumor-promoter properties
    • Zent C.S., Mathieu C., Claxton D.F., Zhang D.E., Tenen D.G., Rowley J.D., et al. The chimeric genes AML1/MDS1 and AML1/EAP inhibit AML1B activation at the CSF1R promoter, but only AML1/MDS1 has tumor-promoter properties. Proc Natl Acad Sci U S A 1996, 93:1044-1048.
    • (1996) Proc Natl Acad Sci U S A , vol.93 , pp. 1044-1048
    • Zent, C.S.1    Mathieu, C.2    Claxton, D.F.3    Zhang, D.E.4    Tenen, D.G.5    Rowley, J.D.6
  • 18
    • 34249081692 scopus 로고    scopus 로고
    • Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome
    • Agerstam H., Lilljebjorn H., Lassen C., Swedin A., Richter J., Vandenberghe P., et al. Fusion gene-mediated truncation of RUNX1 as a potential mechanism underlying disease progression in the 8p11 myeloproliferative syndrome. Genes Chromosomes Cancer 2007, 46:635-643.
    • (2007) Genes Chromosomes Cancer , vol.46 , pp. 635-643
    • Agerstam, H.1    Lilljebjorn, H.2    Lassen, C.3    Swedin, A.4    Richter, J.5    Vandenberghe, P.6
  • 19
    • 25844450207 scopus 로고    scopus 로고
    • Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22)
    • Sakai I., Tamura T., Narumi H., Uchida N., Yakushijin Y., Hato T., et al. Novel RUNX1-PRDM16 fusion transcripts in a patient with acute myeloid leukemia showing t(1;21)(p36;q22). Genes Chromosomes Cancer 2005, 44:265-270.
    • (2005) Genes Chromosomes Cancer , vol.44 , pp. 265-270
    • Sakai, I.1    Tamura, T.2    Narumi, H.3    Uchida, N.4    Yakushijin, Y.5    Hato, T.6
  • 20
    • 33748946538 scopus 로고    scopus 로고
    • Overexpression of PRDM16 in the presence and absence of the RUNX1/PRDM16 fusion gene in myeloid leukemias
    • Hazourli S., Chagnon P., Sauvageau M., Fetni R., Busque L., Hebert J. Overexpression of PRDM16 in the presence and absence of the RUNX1/PRDM16 fusion gene in myeloid leukemias. Genes Chromosomes Cancer 2006, 45:1072-1076.
    • (2006) Genes Chromosomes Cancer , vol.45 , pp. 1072-1076
    • Hazourli, S.1    Chagnon, P.2    Sauvageau, M.3    Fetni, R.4    Busque, L.5    Hebert, J.6
  • 21
    • 41649109612 scopus 로고    scopus 로고
    • Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for cDNA
    • Chinen Y., Taki T., Nishida K., Shimizu D., Okuda T., Yoshida N., et al. Identification of the novel AML1 fusion partner gene, LAF4, a fusion partner of MLL, in childhood T-cell acute lymphoblastic leukemia with t(2;21)(q11;q22) by bubble PCR method for cDNA. Oncogene 2008, 27:2249-2256.
    • (2008) Oncogene , vol.27 , pp. 2249-2256
    • Chinen, Y.1    Taki, T.2    Nishida, K.3    Shimizu, D.4    Okuda, T.5    Yoshida, N.6
  • 22
    • 0028837972 scopus 로고
    • An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms
    • Tanaka T., Tanaka K., Ogawa S., Kurokawa M., Mitani K., Nishida J., et al. An acute myeloid leukemia gene, AML1, regulates hemopoietic myeloid cell differentiation and transcriptional activation antagonistically by two alternative spliced forms. EMBO J 1995, 14:341-350.
    • (1995) EMBO J , vol.14 , pp. 341-350
    • Tanaka, T.1    Tanaka, K.2    Ogawa, S.3    Kurokawa, M.4    Mitani, K.5    Nishida, J.6
  • 23
    • 64849104891 scopus 로고    scopus 로고
    • Overexpression of an isoform of AML1 in acute leukemia and its potential role in leukemogenesis
    • Liu X., Zhang Q., Zhang D.E., Zhou C., Xing H., Tian Z., et al. Overexpression of an isoform of AML1 in acute leukemia and its potential role in leukemogenesis. Leukemia 2009, 23:739-745.
    • (2009) Leukemia , vol.23 , pp. 739-745
    • Liu, X.1    Zhang, Q.2    Zhang, D.E.3    Zhou, C.4    Xing, H.5    Tian, Z.6
  • 24
    • 33644807219 scopus 로고    scopus 로고
    • Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice
    • Yamashita N., Osato M., Huang L., Yanagida M., Kogan S.C., Iwasaki M., et al. Haploinsufficiency of Runx1/AML1 promotes myeloid features and leukaemogenesis in BXH2 mice. Br J Haematol 2005, 131:495-507.
    • (2005) Br J Haematol , vol.131 , pp. 495-507
    • Yamashita, N.1    Osato, M.2    Huang, L.3    Yanagida, M.4    Kogan, S.C.5    Iwasaki, M.6
  • 25
    • 67049162141 scopus 로고    scopus 로고
    • High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder
    • Preudhomme C., Renneville A., Bourdon V., Philippe N., Roche-Lestienne C., Boissel N., et al. High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder. Blood 2009, 113:5583-5587.
    • (2009) Blood , vol.113 , pp. 5583-5587
    • Preudhomme, C.1    Renneville, A.2    Bourdon, V.3    Philippe, N.4    Roche-Lestienne, C.5    Boissel, N.6
  • 26
    • 33749583795 scopus 로고    scopus 로고
    • The putative chloride channel hCLCA2 has a single C-terminal transmembrane segment
    • Elble R.C., Walia V., Cheng H.C., Connon C.J., Mundhenk L., Gruber A.D., et al. The putative chloride channel hCLCA2 has a single C-terminal transmembrane segment. J Biol Chem 2006, 281:29448-29454.
    • (2006) J Biol Chem , vol.281 , pp. 29448-29454
    • Elble, R.C.1    Walia, V.2    Cheng, H.C.3    Connon, C.J.4    Mundhenk, L.5    Gruber, A.D.6
  • 27
    • 0035816533 scopus 로고    scopus 로고
    • The breast cancer beta 4 integrin and endothelial human CLCA2 mediate lung metastasis
    • Abdel-Ghany M., Cheng H.C., Elble R.C., Pauli B.U. The breast cancer beta 4 integrin and endothelial human CLCA2 mediate lung metastasis. J Biol Chem 2001, 276:25438-25446.
    • (2001) J Biol Chem , vol.276 , pp. 25438-25446
    • Abdel-Ghany, M.1    Cheng, H.C.2    Elble, R.C.3    Pauli, B.U.4
  • 28
    • 0035798627 scopus 로고    scopus 로고
    • Tumor suppression by a proapoptotic calcium-activated chloride channel in mammary epithelium
    • Elble R.C., Pauli B.U. Tumor suppression by a proapoptotic calcium-activated chloride channel in mammary epithelium. J Biol Chem 2001, 276:40510-40517.
    • (2001) J Biol Chem , vol.276 , pp. 40510-40517
    • Elble, R.C.1    Pauli, B.U.2
  • 29
    • 69249100045 scopus 로고    scopus 로고
    • HCLCA2 is a p53-inducible inhibitor of breast cancer cell proliferation
    • Walia V., Ding M., Kumar S., Nie D., Premkumar L.S., Elble R.C. hCLCA2 is a p53-inducible inhibitor of breast cancer cell proliferation. Cancer Res 2009, 69:6624-6632.
    • (2009) Cancer Res , vol.69 , pp. 6624-6632
    • Walia, V.1    Ding, M.2    Kumar, S.3    Nie, D.4    Premkumar, L.S.5    Elble, R.C.6
  • 30
    • 1442308340 scopus 로고    scopus 로고
    • CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancer
    • Li X., Cowell J.K., Sossey-Alaoui K. CLCA2 tumour suppressor gene in 1p31 is epigenetically regulated in breast cancer. Oncogene 2004, 23:1474-1480.
    • (2004) Oncogene , vol.23 , pp. 1474-1480
    • Li, X.1    Cowell, J.K.2    Sossey-Alaoui, K.3


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