Jpn J Cancer Res. 1996 Sep;87(9):887-92. Unique Identifier : AIDSLINE
The precise mechanism of the neoplastic cell growth of adult T cell
leukemia (ATL) still remains unclear. In the present study, we have
succeeded in serial transplantation of ATL cells from a patient into
severe combined immunodeficient (SCID) mice. In this model, we found
that only a leukemic cell clone from an ATL patient could be
successively transplanted into SCID mice, although it was difficult to
maintain leukemic cell clones in vitro, suggesting that the
microenvironment provided by SCID mice is suitable for leukemic cell
growth. We could not detect human T cell leukemia virus type I (HTLV-I)
mRNA or interleukin 2 (IL-2) mRNA in either the tumor cells growing in
mice or the original leukemic cells. Thus, it appears that neither
HTLV-I viral expression nor the IL-2 autocrine mechanism is directly
involved in the neoplastic cell growth of fresh ATL cells as well as
HTLV-I-infected cell lines, at least in SCID mice. In addition, we could
passage frozen cells and obtain a large number of expanded leukemic
cells in this model. Such a serial transplantation model, which can
avoid the changes in the nature of leukemic cells that are frequently
observed in in vitro culture, and which can propagate leukemic cell
clones, would be very suitable not only to study the mechanism of
neoplastic cell growth, but also to test potential therapeutic agents
for ATL.
Aged Animal Cell Division/PHYSIOLOGY Disease Models, Animal DNA,
Neoplasm/ANALYSIS Female Flow Cytometry Human
HTLV-I/GENETICS/METABOLISM Interleukin-2/GENETICS/METABOLISM Leukemia,
T-Cell/*PATHOLOGY Mice Mice, SCID Neoplasm Transplantation
Polymerase Chain Reaction RNA, Messenger/ANALYSIS Support, Non-U.S.
Gov't Transcription, Genetic Transplantation, Heterologous JOURNAL
ARTICLE