TY - JOUR
T1 - Resistance to platinum-containing chemotherapy in testicular germ cell tumors is associated with downregulation of the protein kinase SRPK1
AU - Schenk, Paul W
AU - Stoop, Hans
AU - Bokemeyer, Carsten
AU - Mayer, Frank
AU - Stoter, Gerrit
AU - Oosterhuis, J Wolter
AU - Wiemer, Erik
AU - Looijenga, Leendert H J
AU - Nooter, Kees
N1 - Copyright 2004 Neoplasia Press, Inc.
PY - 2004/7/17
Y1 - 2004/7/17
N2 - 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.
AB - 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.
KW - Adolescent
KW - Adult
KW - Drug Resistance, Neoplasm
KW - Gene Expression Regulation, Neoplastic
KW - Germinoma/drug therapy
KW - Humans
KW - Immunohistochemistry
KW - Male
KW - Middle Aged
KW - Platinum Compounds/therapeutic use
KW - Protein Serine-Threonine Kinases/genetics
KW - RNA Splicing
KW - Survival Analysis
KW - Testicular Neoplasms/drug therapy
UR - http://www.scopus.com/inward/record.url?scp=3142720339&partnerID=8YFLogxK
U2 - 10.1593/neo.03406
DO - 10.1593/neo.03406
M3 - Article
C2 - 15256051
SN - 1522-8002
VL - 6
SP - 297
EP - 301
JO - Neoplasia (New York, N.Y.)
JF - Neoplasia (New York, N.Y.)
IS - 4
ER -