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From the Dipartimento di Biologia e Patologia Cellulare e
Molecolare "L. Califano" Centro di Endocrinologia ed Oncologia
Sperimentale del CNR "G. Salvatore,"*
Università degli Studi di Napoli "Federico II," Napoli; the
Dipartimento di Scienze Biomorfologiche e Funzionali Sez, Anatomia
Patologica e Citopatologia,
Università
degli Studi di Napoli "Federico II," Napoli; the Istituto Nazionale
dei Tumori di Napoli,
Napoli; the
Dipartimento di Sanità Pubblica e Biologia
Cellulare,
Università di Roma "Tor
Vergata," Rome; and the Dipartimento di Medicina Sperimentale e
Clinica,¶
Università degli Studi di
Catanzaro "Magna Graecia," Italy
The RING-finger protein RNF4 modulates both steroid-receptor-dependent and basal transcription and interacts with a variety of nuclear proteins involved in cell growth control. RNF4 is expressed at very high levels in testis and at much lower levels in several other tissues. We show that in germ cells RNF4 expression is strongly modulated during progression of spermatogonia to spermatids, with a peak in spermatocytes. Analysis of human testicular germ cell tumors shows that RNF4 is not expressed in all tumors analyzed including seminomas, the highly malignant embryonal carcinomas, yolk sac, and mixed germ cell tumors. We also show that the ectopically expressed RNF4 gene inhibits cell proliferation of both somatic and germ cell tumor-derived cells. Mutation of critical cysteine residues in the RING finger domain abolished the RNF4 growth inhibition activity. Our results suggest that the lack of RNF4 expression may play a role in the progression of testicular tumors.
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