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Título
Modelo murino experimental de cáncer renal
Autor(es)
Palabras clave
Renal carcinoma
Experimental model
Validation
Clasificación UNESCO
32 Ciencias Médicas
3213.06 Cirugía Experimental
3213.16 Urología
Fecha de publicación
2017-09
Editor
Elsevier
Citación
Padilla-Fernández, B., García-Cenador, M. B., Rodríguez-Marcos, P., López-Marcos, J. F., Antúnez-Plaza, P., Silva-Abuín, J. M., López-Montañés, D., García-Criado, F. J., & Lorenzo-Gómez, M. F. (2017). Experimental murine model of renal cancer. Modelo murino experimental de cáncer renal. Actas urologicas espanolas, 41(7), 445–450. https://doi.org/10.1016/j.acuro.2016.11.005
Resumen
[EN]Introduction: The objective of this study was to determine the reproducibility in a murine
model of renal tumors of various histological strains that could be useful for investigating the
response to target drugs.
Material and methods: Development and analysis of the ‘‘in vivo’’ model: tumor xenograft
of renal cell carcinomas with Balb/c nude athymic mice. Nontumourous human renal tissue
was implanted in the interscapular region of 5 mice, chromophobe renal cell carcinoma was
implanted in 5 mice (which, after checking its growth, was prepared for implantation in another
10 mice) and Fuhrman grade 2 clear cell renal cell carcinoma (CCRCC) was implanted in 5 mice
(which was also subsequently implanted in 10 mice).
We monitored the tumor size, onset of metastases and increase in size and number of tumors.
When the size had reached a point greater than or equal to locally advanced or metastatic
carcinoma, the animals were euthanised for a pathological and immunohistochemical study
and a second phase of implantation.
Results: The subcutaneous xenograft of the healthy tissue did not grow. The animals were
euthanised at 6 months and no renal tissue was found. The chromophobe renal cell carcinoma
cells grew in the initial phase (100%); however, in the second phase, we observed a chronic
lymphomonocyte inflammatory reaction and a foreign body reaction. The CCRCC grew at 5---8
months both in the first and second phase (100%), maintaining the tumor type and grade.
Conclusions: The model with athymic Balb/c nude mice is useful for reproducing CCRCC, with
the same histological characteristics and aggressiveness as native human tumors, promoting
the development of the second experimental phase.
URI
ISSN
0210-4806
DOI
10.1016/j.acuro.2016.11.005
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