TY - JOUR
T1 - The tumor microenvironment
T2 - Possible role of integrins and the extracellular matrix in tumor biological behavior of intratubular germ cell neoplasia and testicular seminomas
AU - Timmer, Albertus
AU - Oosterhuis, J. Wolter
AU - Koops, Heimen Schraffordt
AU - Sleijfer, Dirk Th
AU - Szabo, Ben G.
AU - Timens, Wim
PY - 1994/5
Y1 - 1994/5
N2 - In the present study, we examined the distribution of integrin subunits and extracellular matrix proteins in normal testis, intratubular germ cell neoplasia (ITGCN), and primary and metastatic seminomas. Compared to normal testis in ITGCN, Sertoli cells showed increased expression of α3, α6, and β1 integrin subunits. Malignant intratubular germ cells stained for α3, α6, and β1 integrin subunits. Progression of ITGCN to invasive seminoma was associated with loss of α3 integrin subunit expression by tumor cells. Consequent to this loss, it can be speculated that the strong expression on ITGCN may be related to the noninvasive character of the lesion as is also known from other noninvasive tumors. All tumors showed a strong expression of α6 and β1 integrin subunits. The α5 integrin subunit was weakly expressed in primary seminomas in all stages. No differences were observed in integrin expression between primary and metastatic tumors. The distribution of extracellular matrix proteins was heterogeneous and revealed clear architectural differences between seminomas that may reflect different stages of tumor stroma formation. To our knowledge, the results presented in this study provide the first information on the possible role of tumor- extracellular matrix interactions in the biological behavior of ITGCN and testicular seminomas.
AB - In the present study, we examined the distribution of integrin subunits and extracellular matrix proteins in normal testis, intratubular germ cell neoplasia (ITGCN), and primary and metastatic seminomas. Compared to normal testis in ITGCN, Sertoli cells showed increased expression of α3, α6, and β1 integrin subunits. Malignant intratubular germ cells stained for α3, α6, and β1 integrin subunits. Progression of ITGCN to invasive seminoma was associated with loss of α3 integrin subunit expression by tumor cells. Consequent to this loss, it can be speculated that the strong expression on ITGCN may be related to the noninvasive character of the lesion as is also known from other noninvasive tumors. All tumors showed a strong expression of α6 and β1 integrin subunits. The α5 integrin subunit was weakly expressed in primary seminomas in all stages. No differences were observed in integrin expression between primary and metastatic tumors. The distribution of extracellular matrix proteins was heterogeneous and revealed clear architectural differences between seminomas that may reflect different stages of tumor stroma formation. To our knowledge, the results presented in this study provide the first information on the possible role of tumor- extracellular matrix interactions in the biological behavior of ITGCN and testicular seminomas.
UR - http://www.scopus.com/inward/record.url?scp=0028271833&partnerID=8YFLogxK
M3 - Article
C2 - 8178927
AN - SCOPUS:0028271833
SN - 0002-9440
VL - 144
SP - 1035
EP - 1044
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 5
ER -