TY - JOUR
T1 - Aberrant platelet-derived growth factor alpha-receptor transcript as a diagnostic marker for early human germ cell tumors of the adult testis
AU - Mosselman, S
AU - Looijenga, L H
AU - Gillis, A J
AU - van Rooijen, M A
AU - Kraft, H J
AU - van Zoelen, E J
AU - Oosterhuis, J W
PY - 1996/4/2
Y1 - 1996/4/2
N2 - Testicular germ cell tumors are the most common form of cancer in young adult males. They result from a derangement of primordial germ cells, and they grow out from a noninvasive carcinoma-in-situ precursor. Since carcinoma in situ can readily be cured by low-dose irradiation, there is a great incentive for non- or minimally invasive methods for detection of carcinoma in situ. We have recently shown that human Tera-2 embryonal carcinoma cells, obtained from a nonseminomatous testicular germ cell tumor, show alternative splicing and alternative promoter use of the platelet-derived growth factor alpha-receptor gene, giving rise to a unique 1.5-kb transcript. In this study we have set up a reverse transcriptase-polymerase chain reaction strategy for characterization of the various transcripts for this receptor. Using this technique, we show that a panel of 18 seminomas and II nonseminomatous testicular germ cell tumors all express the 1.5-kb transcript. In addition, a panel of 27 samples of testis parenchyma with established carcinoma in situ were all found to be positive for the 1.5-kb transcript, while parenchyma lacking carcinoma in situ, placenta, and control semen were all negative. These data show that the 1.5-kb platelet-derived growth factor alpha-receptor transcript can be used as a highly selective marker for detection of early stages of human testicular germ cell tumors.
AB - Testicular germ cell tumors are the most common form of cancer in young adult males. They result from a derangement of primordial germ cells, and they grow out from a noninvasive carcinoma-in-situ precursor. Since carcinoma in situ can readily be cured by low-dose irradiation, there is a great incentive for non- or minimally invasive methods for detection of carcinoma in situ. We have recently shown that human Tera-2 embryonal carcinoma cells, obtained from a nonseminomatous testicular germ cell tumor, show alternative splicing and alternative promoter use of the platelet-derived growth factor alpha-receptor gene, giving rise to a unique 1.5-kb transcript. In this study we have set up a reverse transcriptase-polymerase chain reaction strategy for characterization of the various transcripts for this receptor. Using this technique, we show that a panel of 18 seminomas and II nonseminomatous testicular germ cell tumors all express the 1.5-kb transcript. In addition, a panel of 27 samples of testis parenchyma with established carcinoma in situ were all found to be positive for the 1.5-kb transcript, while parenchyma lacking carcinoma in situ, placenta, and control semen were all negative. These data show that the 1.5-kb platelet-derived growth factor alpha-receptor transcript can be used as a highly selective marker for detection of early stages of human testicular germ cell tumors.
KW - Adult
KW - Alkaline Phosphatase/analysis
KW - Base Sequence
KW - Biomarkers, Tumor/analysis
KW - Carcinoma, Embryonal
KW - Choriocarcinoma/metabolism
KW - Clone Cells
KW - DNA Primers
KW - Gene Expression
KW - Germinoma/classification
KW - Humans
KW - Male
KW - Molecular Sequence Data
KW - Polymerase Chain Reaction
KW - Receptor, Platelet-Derived Growth Factor alpha
KW - Receptors, Platelet-Derived Growth Factor/analysis
KW - Seminiferous Tubules/cytology
KW - Seminoma/metabolism
KW - Teratoma/metabolism
KW - Testicular Neoplasms/classification
KW - Testis/cytology
KW - Transcription, Genetic
KW - Tretinoin/pharmacology
KW - Tumor Cells, Cultured
UR - http://www.scopus.com/inward/record.url?scp=0029865425&partnerID=8YFLogxK
U2 - 10.1073/pnas.93.7.2884
DO - 10.1073/pnas.93.7.2884
M3 - Article
C2 - 8610136
SN - 0027-8424
VL - 93
SP - 2884
EP - 2888
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 7
ER -