Amb motiu del tancament d'estiu, la validació de documents es reprendrà a partir del 28 d'agost de 2026. Disculpeu les molèsties.
Con motivo del cierre de verano, la validación de documentos se reanudará a partir del 28 de agosto de 2026. Disculpad las molestias
Due to the summer closure, document validation will resume starting August 28, 2026. We apologize for any inconvenience.

Document type

Article

Version

Published version

Publication date

Publication license

cc-by-nc-nd (c) Universidad de Murcia, 1997
Please use this identifier to cite or link to this item: https://hdl.handle.net/2445/104402

k-FGF protoncogene expression is associated with murine testicular teratogenesis, but is not involved during mouse testicular development

Journal Title

Director/Tutor

Journal ISSN

Volume Title

Related resource

Abstract

The k-FGF gene, which belongs to the family of the fibroblast growth factor genes, is implicated in tumoral and developmental processes. It is expressed in embryonal carcinoma cells, in embryonic stem cells, during limb and tooth formation and in some germ cell tumors. However, the expression of this protooncogene during testicular development as well its relationship to spontaneous teratogenesis have not been determined. Here we investigate k-FGF xpression during testicular development in mice, as well as in a spontaneous testicular teratoma (STT) and in the OTT6050 teratocarcinoma (TC) by Northern blotting, RT-PCR and in situ hybridization. Severa1 data indicate that k-FGF gene contains downstream regulatory sequences which bind octamer factors. One of these transcription factors which binds to k-FGF enhancer is Oct-4. Although the k-FGF gene is activated by Oct-4 in embryonal carcinoma and embryonic stem cells and Oct-4 is expressed in the germ cells of the embryo, our results indicate that there is no detectable k-FGF expression in mouse testicular germ cells at any stage of development. This indicates that Oct-4 does not activate transcription of the k-FGF gene in mouse germ cells, and that k-FGF is not implicated during testicular development. We also show that there is a high k-FGF expression in the experimental OTT6050 TC, but only very low levels in a murine differentiated STT, suggesting that k-FGF activation may be responsible for the genesis and development of STT, behaving as a marker of malignancy in these neoplasms.

Description

A l'article en PDF consta com a vol.11 (1996)

Citation

Citation

ANTA I VINYALS, Josep Maria de, et al. k-FGF protoncogene expression is associated with murine testicular teratogenesis, but is not involved during mouse testicular development. Histology and Histopathology. 1997. Vol. 12, num. 1, pags. 32-41. ISSN 0213-3911. [consulted: 16 of August of 2026]. Available at: https://hdl.handle.net/2445/104402

Export metadata

JSON - METS

Share record