Resistance to platinum-containing chemotherapy in testicular germ cell tumors is associated with downregulation of the protein kinase SRPK1

Paul W Schenk, Hans Stoop, Carsten Bokemeyer, Frank Mayer, Gerrit Stoter, J Wolter Oosterhuis, Erik Wiemer, Leendert H J Looijenga, Kees Nooter

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

Samenvatting

Male germ cell tumors (GCTs) are extremely sensitive to platinum-containing chemotherapy, with only 10% of patients showing therapy resistance. However, the biological basis of the high curability of disseminated GCTs by chemotherapy is still unknown. Recently, we demonstrated that the mammalian serine/arginine-rich protein-specific kinase 1 (SRPK1) is a cisplatin-sensitive gene, inactivation of which leads to cisplatin resistance. Because, in mammalians, the expression of SRPK1 is preferentially high in testicular tissues, cisplatin responsiveness of male GCTs might be associated with SRPK1 levels. In the present study, we monitored SRPK1 protein expression in a unique series of nonseminomatous GCTs by immunohistochemistry. Randomly selected GCTs (n = 70) and tumors from patients responding to standard chemotherapy (n = 20) generally showed strong SRPK1 staining. In contrast, expression in refractory GCTs (n = 20) as well as in GCTs from poor-prognosis patients responding to high-dose chemotherapy only (n = 11) was significantly lower (two-sided Wilcoxon rank sum test: P < .001). In conclusion, our data suggest that SRPK1 expression might be an important prognostic indicator for the chemoresponsiveness of nonseminomatous GCTs.

Originele taal-2Engels
Pagina's (van-tot)297-301
Aantal pagina's5
TijdschriftNeoplasia (New York, N.Y.)
Volume6
Nummer van het tijdschrift4
DOI's
StatusGepubliceerd - 17 jul. 2004
Extern gepubliceerdJa

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