TY - JOUR
T1 - JKT-1 is not a human seminoma cell line
AU - de Jong, Jeroen
AU - Stoop, Hans
AU - Gillis, Ad J M
AU - van Gurp, Ruud J H L M
AU - van Drunen, Ellen
AU - Beverloo, H Berna
AU - Lau, Yun-Fai Chris
AU - Schneider, Dominik T
AU - Sherlock, Jon K
AU - Baeten, John
AU - Hatakeyama, Shingo
AU - Ohyama, Chikara
AU - Oosterhuis, J Wolter
AU - Looijenga, Leendert H J
PY - 2007/8
Y1 - 2007/8
N2 - The JKT-1 cell line has been used in multiple independent studies as a representative model of human testicular seminoma. However, no cell line for this specific tumour type has been independently confirmed previously; and therefore, the seminomatous origin of JKT-1 must be proven. The genetic constitution of the JKT-1 cells was determined using flow cytometry and spectral karyotyping, as well as array comparative genomic hybridization and fluorescent in situ hybridization. Marker profiling, predominantly based on differentially expressed proteins during normal germ cell development, was performed by immunohistochemistry and Western blot analyses. Moreover, genome wide affymetrix mRNA expression and profiling of 157 microRNAs was performed, and the status of genomic imprinting was determined. A germ cell origin of the JKT-1 cells was in line with genomic imprinting status and marker profile (including positive staining for several cancer-testis antigens). However, the supposed primary tumour, from which the cell line was derived, being indeed a classical seminoma, was molecularly proven not to be the origin of the cell line. The characteristic chromosomal anomalies of seminoma, e.g. gain of the short arm of chromosome 12, as well as the informative marker profile (positive staining for OCT3/4, NANOG, among others) were absent in the various JKT-1 cell lines investigated, irrespective of where the cells were cultured. All results indicate that the JKT-1 cell line is not representative of human seminoma. Although it can originate from an early germ cell, a non-germ cell derivation cannot be excluded.
AB - The JKT-1 cell line has been used in multiple independent studies as a representative model of human testicular seminoma. However, no cell line for this specific tumour type has been independently confirmed previously; and therefore, the seminomatous origin of JKT-1 must be proven. The genetic constitution of the JKT-1 cells was determined using flow cytometry and spectral karyotyping, as well as array comparative genomic hybridization and fluorescent in situ hybridization. Marker profiling, predominantly based on differentially expressed proteins during normal germ cell development, was performed by immunohistochemistry and Western blot analyses. Moreover, genome wide affymetrix mRNA expression and profiling of 157 microRNAs was performed, and the status of genomic imprinting was determined. A germ cell origin of the JKT-1 cells was in line with genomic imprinting status and marker profile (including positive staining for several cancer-testis antigens). However, the supposed primary tumour, from which the cell line was derived, being indeed a classical seminoma, was molecularly proven not to be the origin of the cell line. The characteristic chromosomal anomalies of seminoma, e.g. gain of the short arm of chromosome 12, as well as the informative marker profile (positive staining for OCT3/4, NANOG, among others) were absent in the various JKT-1 cell lines investigated, irrespective of where the cells were cultured. All results indicate that the JKT-1 cell line is not representative of human seminoma. Although it can originate from an early germ cell, a non-germ cell derivation cannot be excluded.
KW - Cell Line, Tumor
KW - Humans
KW - Immunohistochemistry
KW - Karyotyping
KW - Male
KW - Models, Biological
KW - Reproducibility of Results
KW - Seminoma
KW - Testicular Neoplasms
U2 - 10.1111/j.1365-2605.2007.00802.x
DO - 10.1111/j.1365-2605.2007.00802.x
M3 - Article
C2 - 17705808
SN - 0105-6263
VL - 30
SP - 350
EP - 365
JO - International journal of andrology
JF - International journal of andrology
IS - 4
ER -