A. Sakashita et al., AMPLIFICATION OF THE TCL1 FLANKING REGION AT 14Q32.1 WITH NO TCL1 GENE-TRANSCRIPTION IN A PATIENT WITH PERIPHERAL T-CELL LYMPHOMA, Leukemia, 12(6), 1998, pp. 970-971
Cytogenetic and molecular-genetic characteristics in peripheral T cell
lymphoma (PTL) have not been well defined, except for those in adult
T cell leukemia/lymphoma (ATL/L). Translocations and inversions involv
ing a chromosome band 14q32 were extremely common abnormalities report
ed in PTL and ATL/L. We studied the involvement of TCL1, a recently is
olated gene located in 14q32.1, in tumor tissues from 20 patients with
PTL including three with 14q32 translocations by two color fluorescen
t in situ hybridization (FISH) using two cosmid probes flanking the TC
L1 gene. The two cosmid signals were separated in none of them, but mu
ch increased in number in one tumor without 14q32 translocation, indic
ating that the TCL1 genomic region was amplified in this tumor. Revers
e transcription-polymerase chain reaction (RT-PCR), however, failed to
detect the TCL1 transcript in the tumor. These findings suggest that
an oncogene other than TCL1 may be located in 14q32.1, and its amplifi
cation may be involved in the neoplastic process of PTL.