An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse.

Standard

An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse. / Bittner, Cordula; Feller, A C; Renauld, J C; Lange, K; Pietrzik, R; Jenetzky, C; Briese, J; Gaiser, T; Müller, A; Wiedemann, G J; Van Snick, J; Merz, H.

in: LAB INVEST, Jahrgang 80, Nr. 10, 10, 2000, S. 1523-1531.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Bittner, C, Feller, AC, Renauld, JC, Lange, K, Pietrzik, R, Jenetzky, C, Briese, J, Gaiser, T, Müller, A, Wiedemann, GJ, Van Snick, J & Merz, H 2000, 'An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse.', LAB INVEST, Jg. 80, Nr. 10, 10, S. 1523-1531. <http://www.ncbi.nlm.nih.gov/pubmed/11045569?dopt=Citation>

APA

Bittner, C., Feller, A. C., Renauld, J. C., Lange, K., Pietrzik, R., Jenetzky, C., Briese, J., Gaiser, T., Müller, A., Wiedemann, G. J., Van Snick, J., & Merz, H. (2000). An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse. LAB INVEST, 80(10), 1523-1531. [10]. http://www.ncbi.nlm.nih.gov/pubmed/11045569?dopt=Citation

Vancouver

Bittner C, Feller AC, Renauld JC, Lange K, Pietrzik R, Jenetzky C et al. An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse. LAB INVEST. 2000;80(10):1523-1531. 10.

Bibtex

@article{774bf6bb0d334c6cbd9a1d92cdb5c598,
title = "An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse.",
abstract = "We report on the analysis of a murine anaplastic lymphoid cell line TS1G6, established recently by interleukin (IL)-9 transfection. TS1G6 revealed a highly characteristic pattern of large anaplastic cells with mononuclear, binuclear, or multinuclear cells resembling Hodgkin (H) or Sternberg-Reed (SR) cells. This cell line is tumorigenous after injection of as few as 10(4) lymphoma cells into nude or immunocompetent C57Bl/6 mice and leads to death from progressive disease of all treated animals within a few weeks. The histological analysis of these tumors revealed a diffuse large cell malignant lymphoma that is morphologically almost identical to human anaplastic large cell lymphoma (ALCL). The lymphoma cells did not show overexpression of the anaplastic lymphoma kinase (ALK) gene, which is found in about 50% of the cases of human ALCL. Thus, this model may be an animal model for an important subset of human ALCL. The cytokine profile, which is of the T helper 2 type, showed strong parallels to the human lymphoma counterpart. Mice suffering from such lymphomas could not be cured with a regimen using high dose cyclophosphamide similar to many ALCL patients. Such an animal model for ALCL has not yet been recognized, but may provide the basis for investigating new antitumor immunotherapies in a fully immunocompetent host.",
author = "Cordula Bittner and Feller, {A C} and Renauld, {J C} and K Lange and R Pietrzik and C Jenetzky and J Briese and T Gaiser and A M{\"u}ller and Wiedemann, {G J} and {Van Snick}, J and H Merz",
year = "2000",
language = "Deutsch",
volume = "80",
pages = "1523--1531",
journal = "LAB INVEST",
issn = "0023-6837",
publisher = "NATURE PUBLISHING GROUP",
number = "10",

}

RIS

TY - JOUR

T1 - An animal model for anaplastic large cell lymphoma in the immunocompetent syngeneic C57Bl/6 mouse.

AU - Bittner, Cordula

AU - Feller, A C

AU - Renauld, J C

AU - Lange, K

AU - Pietrzik, R

AU - Jenetzky, C

AU - Briese, J

AU - Gaiser, T

AU - Müller, A

AU - Wiedemann, G J

AU - Van Snick, J

AU - Merz, H

PY - 2000

Y1 - 2000

N2 - We report on the analysis of a murine anaplastic lymphoid cell line TS1G6, established recently by interleukin (IL)-9 transfection. TS1G6 revealed a highly characteristic pattern of large anaplastic cells with mononuclear, binuclear, or multinuclear cells resembling Hodgkin (H) or Sternberg-Reed (SR) cells. This cell line is tumorigenous after injection of as few as 10(4) lymphoma cells into nude or immunocompetent C57Bl/6 mice and leads to death from progressive disease of all treated animals within a few weeks. The histological analysis of these tumors revealed a diffuse large cell malignant lymphoma that is morphologically almost identical to human anaplastic large cell lymphoma (ALCL). The lymphoma cells did not show overexpression of the anaplastic lymphoma kinase (ALK) gene, which is found in about 50% of the cases of human ALCL. Thus, this model may be an animal model for an important subset of human ALCL. The cytokine profile, which is of the T helper 2 type, showed strong parallels to the human lymphoma counterpart. Mice suffering from such lymphomas could not be cured with a regimen using high dose cyclophosphamide similar to many ALCL patients. Such an animal model for ALCL has not yet been recognized, but may provide the basis for investigating new antitumor immunotherapies in a fully immunocompetent host.

AB - We report on the analysis of a murine anaplastic lymphoid cell line TS1G6, established recently by interleukin (IL)-9 transfection. TS1G6 revealed a highly characteristic pattern of large anaplastic cells with mononuclear, binuclear, or multinuclear cells resembling Hodgkin (H) or Sternberg-Reed (SR) cells. This cell line is tumorigenous after injection of as few as 10(4) lymphoma cells into nude or immunocompetent C57Bl/6 mice and leads to death from progressive disease of all treated animals within a few weeks. The histological analysis of these tumors revealed a diffuse large cell malignant lymphoma that is morphologically almost identical to human anaplastic large cell lymphoma (ALCL). The lymphoma cells did not show overexpression of the anaplastic lymphoma kinase (ALK) gene, which is found in about 50% of the cases of human ALCL. Thus, this model may be an animal model for an important subset of human ALCL. The cytokine profile, which is of the T helper 2 type, showed strong parallels to the human lymphoma counterpart. Mice suffering from such lymphomas could not be cured with a regimen using high dose cyclophosphamide similar to many ALCL patients. Such an animal model for ALCL has not yet been recognized, but may provide the basis for investigating new antitumor immunotherapies in a fully immunocompetent host.

M3 - SCORING: Zeitschriftenaufsatz

VL - 80

SP - 1523

EP - 1531

JO - LAB INVEST

JF - LAB INVEST

SN - 0023-6837

IS - 10

M1 - 10

ER -