Impaired Lymphocytes Development and Xenotransplantation of Gastrointestinal Tumor Cells in Prkdc-Null SCID Zebrafish Model

Neoplasia (United States)

Volumn 18, Issue 8, 2016, Pages 468-479

  Jung, In Hye ^a   Chung, Yong Yoon ^b   Jung, Dawoon E ^a   Kim, Young Jin ^c   Kim, Do Hee ^d   Kim, Kyung Sik ^a   Park, Seung Woo ^a  

^a Yonsei University College of Medicine   (South Korea)

^b BioCore Company   (South Korea)

^c University of Rochester   (United States)

^d Yonsei University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CD2 ASSOCIATED PROTEIN; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE; PROTEIN KINASE; PROTEIN KINASE DNA ACTIVATED CATALYTIC POLYPEPTIDE; TRANSCRIPTION ACTIVATOR LIKE EFFECTOR NUCLEASE; UNCLASSIFIED DRUG; DNA DEPENDENT PROTEIN KINASE; NUCLEAR PROTEIN; PRKDC PROTEIN, HUMAN;

ADULT; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; B LYMPHOCYTE; CANCER CELL LINE; CONTROLLED STUDY; EXON; GASTROINTESTINAL TUMOR; GENE FUNCTION; GENE MUTATION; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN CELL; IMMUNE DEFICIENCY; IN VIVO STUDY; MOUSE; MUTATION; NONHUMAN; PHENOTYPIC VARIATION; PRIORITY JOURNAL; RAT; SCID MOUSE; SEVERE COMBINED IMMUNODEFICIENCY; SOLID TUMOR; T LYMPHOCYTE; TUMOR GROWTH; TUMOR XENOGRAFT; XENOTRANSPLANTATION; ZEBRA FISH; ANIMAL; BIOPSY; DEFICIENCY; DISEASE MODEL; GENE TARGETING; GENETICS; IMMUNOLOGY; LYMPHOCYTE; METABOLISM; NATURAL KILLER CELL; PATHOLOGY; PHENOTYPE; PROCEDURES; TRANSGENIC ANIMAL; TUMOR CELL LINE; XENOGRAFT;

ANIMALS; ANIMALS, GENETICALLY MODIFIED; BIOPSY; CELL LINE, TUMOR; DISEASE MODELS, ANIMAL; DNA-ACTIVATED PROTEIN KINASE; GASTROINTESTINAL NEOPLASMS; GENE TARGETING; HUMANS; KILLER CELLS, NATURAL; LYMPHOCYTES; NUCLEAR PROTEINS; PHENOTYPE; TRANSPLANTATION, HETEROLOGOUS;

EID: 84979752603     PISSN: 15228002     EISSN: 14765586     Source Type: Journal    
DOI: 10.1016/j.neo.2016.06.007     Document Type: Article

References (32)

1. [1] Jeggo, P, Lavin, MF, Cellular radiosensitivity: how much better do we understand it?. Int J Radiat Biol 85:12 (2009), 1061–1081.
2. [2] Mahaney, BL, Meek, K, Lees-Miller, SP, Repair of ionizing radiation-induced DNA double-strand breaks by non-homologous end-joining. Biochem J 417:3 (2009), 639–650.
3. [3] Soulas-Sprauel, P, Rivera-Munoz, P, Malivert, L, Le Guyader, G, Abramowski, V, Revy, P, de Villartay, JP, V(D)J and immunoglobulin class switch recombinations: a paradigm to study the regulation of DNA end-joining. Oncogene 26:56 (2007), 7780–7791.
4. [4] Franco, S, Alt, FW, Manis, JP, Pathways that suppress programmed DNA breaks from progressing to chromosomal breaks and translocations. DNA Repair (Amst) 5 (2006), 1030–1041.
5. [5] Mashimo, T, Takizawa, A, Kobayashi, J, Kunihiro, Y, Yoshimi, K, Ishida, S, Tanabe, K, Yanagi, A, Tachibana, A, Hirose, J, et al. Generation and characterization of severe combined immunodeficiency rats. Cell Rep 2 (2012), 685–694.
6. [6] Bastide, C, Bagnis, C, Mannoni, P, Hassoun, J, Bladou, F, A nod scid mouse model to study human prostate cancer. Prostate Cancer Prostatic Dis 5 (2002), 311–315.
7. [7] Lee, CH, Xue, H, Sutcliffe, M, Gout, PW, Huntsman, DG, Miller, DM, Gilks, CB, Wang, YZ, Establishment of subrenal capsule xenografts of primary human ovarian tumors in SCID mice: potential models. Gynecol Oncol 96 (2005), 48–55.
8. [8] Lozupone, F, Pende, D, Burgio, VL, Castelli, C, Spada, M, Venditti, M, Luciani, F, Lugini, L, Federici, C, Ramoni, C, et al. Effect of human natural killer and γδ T cells on the growth of human autologous melanoma xenografts in SCID mice. Cancer Res 64 (2004), 378–385.
9. [9] Forest, V, Peoc'h, M, Campos, L, Guvotat, D, Vergnon, JM, Effects of cryotherapy or chemotherapy on apoptosis in a non–small-cell lung cancer xenografted into SCID mice. Cryobiology 50 (2005), 29–37.
10. [10] Rebouissou, C, Wijdenes, J, Autissier, P, Tarte, K, Costes, V, Liautard, J, Rossi, JF, Brochier, J, Klein, B, A gp130 interleukin-6 transducer dependent SCID model of human multiple myeloma. Blood 91 (1998), 4727–4737.
11. [11] Ochiai, M, Ubagai, T, Kawamori, T, Imai, H, Sugimura, T, Nakagama, H, High susceptibility of SCID mice to colon carcinogenesis induced by azoxymethane indicates a possible caretaker role for DNA-dependent protein kinase. Carcinogenesis 22 (2001), 1551–1555.
12. [12] Wacheck, V, Heere-Ress, E, Halaschek-Wiener, J, Lucas, T, Meyer, H, Eichler, HG, Jansen, B, Bcl-2 antisense oligonucleotides chemosensitize human gastric cancer in a SCID mouse xenotransplantation model. J Mol Med 79 (2001), 587–593.
13. [13] Workman, P, Aboagye, EO, Balkwill, F, Guidelines for the welfare and use of animals in cancer research. Br J Cancer 102 (2010), 1555–1577.
14. [14] Trede, NS, Langenau, DM, Traver, D, Look, AT, Zon, LI, The use of zebrafish to understand Immunity. Immunity 20 (2004), 367–379.
15. [15] Traver, D, Paw, BH, Poss, KD, Penberthy, WT, Lin, S, Zon, LI, Transplantation and in vivo imaging of multileneage engraftment in zebrafish bloodless mutants. Nat Immunol 4 (2003), 1238–1246.
16. [16] Petrie-Hanson, L, Hohn, C, Hanson, L, Characterization of rag1 mutant zebrafish leukocytes. BMC Immunol 10 (2009), 1–8.
17. [17] Tang, Q, Abdelfattah, NS, Blackburn, JS, Moore, JC, Martinez, SA, Moore, FE, Lobbardi, R, Tenente, IM, Ignatius, MS, Berman, JN, et al. Optimized cell ransplantation using adult rag2 mutant zebrafish. Nat Methods 11:8 (2014), 821–824.
18. [18] Christian, M, Cermak, T, Doyle, EL, Schmidt, C, Zhang, F, Hummel, A, Bogdanove, AJ, Voytas, DF, Targeting DNA doublestrand breaks with TAL effector nucleases. Genetics 186 (2010), 757–761.
19. [19] Jinek, M, Chylinski, K, Fonfara, I, Hauer, M, Doudna, JA, Charpentier, E, A programmable dual-RNA–guided DNA endonuclease in adaptive bacterial immunity. Science 337 (2012), 816–821.
20. [20] Jung, IH, Jung, DE, Park, YN, Song, SY, Park, SW, Aberrant Hedgehog ligand induce progressive pancreatic fibrosis by paracrine activation of myofibrolasts and ductular cells in transgenic zebrafish. PLoS One 6 (2011), 1–15.
21. [21] Park, SW, Davison, JM, Rhee, J, Hruban, RH, Maitra, A, Leach, SD, Oncogenic KRAS induces progenitor cell expansion and malignant transformation in zebrafish exocrine pancreas. Gastroenterology 134 (2008), 2080–2090.
22. [22] Airaksinen, S, Rabergh, CMI, Sistonen, L, Nikinmaa, M, Effects of heat shock and hypoxia on protein synthesis in rainbow trout (Oncorhynchus mykiss) cells. J Exp Biol 201 (1998), 2543–2551.
23. [23] Jung, IH, Choi, JH, Chung, YY, Lim, GL, Park, YN, Park, SW, Predominant activation of JAK/STAT3 pathway by interleukin-6 is implicated in hepatocarcinogenesis. Neoplasia 17:7 (2015), 586–597.
24. [24] Belizario, JE, Immunodeficient mouse model: an overview. Open Immuno J 2 (2009), 79–85.
25. [25] Stoletov, K, Klemke, R, Catch of the day: zebrafish as a human cancer model. Oncogene, 2008, 1–12.
26. [26] Konantz, M, Balci, TB, Hartwig, UF, Dellaire, G, André, MC, Berman, JN, Lengerke, C, Zebrafish xenografts as a tool for in vivo studies on human cancer. Ann N Y Acad Sci 1266 (2012), 124–137.
27. [27] Yang, XJ, Cui, W, Gu, A, Xu, C, Yu, SC, Li, TT, Cui, YH, Zhang, X, Bian, XW, A novel zebrafish xenotransplantation model for study of glioma stem cell invasion. PLoS One, 8(4), 2013, e61801.
28. [28] Drabsch, Y, He, S, Zhang, L, Snaar-Jagalska, BE, ten Dijke, P, Transforming growth factor-β signalling controls human breast cancer metastasis in a zebrafish xenograft model. Breast Cancer Res, 15(6), 2013, R106, 10.1186/bcr3573.
29. [29] Zhang, B, Shimada, Y, Kuroyanagi, J, Nishimura, Y, Umemoto, N, Nomoto, T, Shintou, T, Miyazaki, T, Tanaka, T, Zebrafish xenotransplantation model for cancer stem-like cell study and high-throughput screening of inhibitors. Tumor Biol 35 (2014), 11861–11869.
30. [30] White, RM, Sessa, A, Burke, C, Bowman, T, LeBlanc, J, Ceol, C, Bourque, C, Dovey, M, Goessling, W, Burns, CE, et al. Transparent adult zebrafish as a tool for in vivo transplantation analysis. Cell Stem Cell 2:2 (2008), 183–189.
31. [31] Heilmann, S, Ratnakumar, K, Langdon, EM, Kansler, ER, Kim, IS, Campbell, NR, Perry, EB, McMahon, AJ, Kaufman, CK, van Rooijen, E, et al. A quantitative system for studying metastasis using transparent zebrafish. Cancer Res 75:20 (2015), 4272–4282.
32. [32] Yang, XJ, Cui, W, Gu, A, Xu, C, Yu, SC, Li, TT, Cui, YH, Zhang, X, Bian, XW, A synthetic dl-nordihydroguaiaretic acid (Nordy), inhibits angiogenesis, invasion and proliferation of glioma stem cells within a zebrafish xenotransplantation model. PLoS One, 9(1), 2014, e85759.