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Epstein-Barr
Virus Infection to Epstein-Barr Virus-Negative Nasopharyngeal
Carcinoma Cell Line TW03 Enhances Its Tumorigenicity |














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Norihiro Teramoto, Akihiko Maeda, Keita Kobayashi, Kazuhiko Hayashi,
Takashi Oka, Kiyoshi Takahashi, Kenzo Takada, Georg Klein, and Tadaatsu
Akagi
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Department
of Pathology (NT, KK, KH, TO, KTakah, TA), Okayama University Medical School,
Okayama, Japan; Microbiology and Tumor Biology Center (AM, GK), Karolinska
Institute, Stockholm, Sweden; Department of Virology (KTakad), Cancer Institute,
Hokkaido University School of Medicine, Sapporo, Japan |
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SUMMARY: Almost all nasopharyngeal carcinomas (NPCs) are infected by
Epstein-Barr virus (EBV), but most ex vivo NPC cells lose EBV genomes
during passages. In this study, an EBV-negative NPC cell line, TW03, established
from EBV-carrying NPC was reinfected with EBV by cocultivation with irradiated
Akata cells carrying recombinant EBV containing a neomycin-resistant gene.
The reinfected EBV (+) TW03 cells expressed EBERs and EBNA1, but not EBNA2,
lytic proteins (ZEBRA and EA-D), or LMP1. They had an epithelial appearance
similar to that of EBV (+) TW03 cells. The doubling times of EBV (+) and
EBV (-) TW03 cells were almost identical. However, the EBV (+) TW03 cells
formed larger colonies with ragged contours in anchorage-independent cultures.
An in vitro invasion assay showed that EBV (+) TW03 cells had a higher
invasive activity than EBV (-) TW03 cells (p > 0.001). Both
EBV (-) and EBV (+) TW03 cells formed poorly differentiated squamous cell
carcinomas in SCID and nude mice. EBV (+) TW03 cells showed a higher tumorigenicity
to nude mice (12 of 13) than EBV (-) TW03 cells (1 of 9) (p >
0.001). In the severe combined immunodeficiency (SCID)tumors of EBV (+)
TW03 cells, not all of the tumor cells were EBER-1 positive. EBER-1 was
more frequently detected in the peripheral regions and daughter nodules
of the tumors than in the central areas. The microdissection polymerase
chain reaction showed that the EBER-1-negative TW03 cells in the EBV (+)
TW03 SCID tumors lost EBV genomes. EBER-1-negative cells showed as high
a rate of Ki-67 positivity as EBER-1-positive cells, indicating that the
former were proliferating rather than dead or dying. In horny pearls,
keratinizing cells were ZEBRA-positive and EBER-negative. Loss of EBV
genomes was not associated with squamous differentiation. These data indicated
that reinfection of EBV promotes the tumorigenicity of EBV (-) TW03 cells
by enhancing the invading activity. (Lab Invest 2000, 80: 303-312)
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