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Abstract 404: Murine lymphomas selected by growth rate: Aggressiveness, galectin-1 (Gal-1) expression and response to low doses of cyclophosphamide (Cy)

Authors :
Gabriel A. Rabinovich
Leonardo Hess
Mariana Salatino
Mariano F. Zacarías Fluck
O. Graciela Scharovsky
Eduardo Roggero
Source :
Cancer Research. 70:404-404
Publication Year :
2010
Publisher :
American Association for Cancer Research (AACR), 2010.

Abstract

L-DGE is a spontaneous poorly differentiated murine lymphoma. During tumor growth it develops lymph node metastasis at a low frequency. Gal-1 is an immunomodulatory protein that acts as a regulator of T cell homeostasis and plays an important role in immune tolerance and tumor-immune escape. Overexpression of Gal-1 is associated with tumor progression and metastasis. Based on our previous findings, our aim was to obtain by a divergent selection two L-DGE variants that differ in tumor growth rate in order to study Gal-1 expression as well as their response to Cy. Two selection experiments were carried out. 1) L-DGE was s.c. implanted on 12 BALB/c mice (day 0). On day 14 the tumor displaying the largest volume was chosen as donor for the next passage to 4 mice. This higher-volume-selection was repeated for 25 serial passages, every 14 days and the tumor thus obtained was named L-DGE/M. 2) L-DGE was s.c. implanted on 12 BALB/c mice (day 0). On day 21, the tumor with the lowest growth rate was chosen as a donor and implanted into 6 mice and repeated through 16 serial passages. As a result of this selection L-DGE/L was obtained. We challenged mice (n=20/group) with L-DGE, L-DGE/M and L-DGE/L and studied tumor growth, metastatic capacity, galectin-1 expression and response to a single low dose Cy (25 mg/kg). Tumor volume vs. Time data was adjusted with an exponential curve and the growth rate was calculated. Gal-1 expression was studied by Western Blot in tumor and metastases homogenates. L-DGE/M growth rate was higher than that of L-DGE (p Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr 404.

Details

ISSN :
15387445 and 00085472
Volume :
70
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi...........d553af2fbeca1b0fbde3bfe6c8dc7772