Random integration of HTLV-I provirus; increasing chromosomal instability

• Published in: Cancer letters 1998-10, Vol.132 (1), p.203-212
• Main Authors: Ohshima, Koichi, Ohgami, Akiko, Matsuoka, Masao, Etoh, Ken-ichiro, Utsunomiya, Atae, Makino, Torahiko, Ishiguro, Masako, Suzumiya, Junji, Kikuchi, Masahiro
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Chromosome abnormality; Hematologic and hematopoietic diseases; HTLV-I; Human T-lymphotropic virus 1; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis; Medical sciences; Random integration
• ISSN: 0304-3835; 1872-7980
• DOI: 10.1016/S0304-3835(98)00188-8

Adult T-cell leukemia/lymphoma (ATLL) is a neoplasm of mature helper (CD4) T-lymphocytes. Human T-cell lymphotropic virus type-I (HTLV-I) is etiologically considered to cause ATLL. It has been suggested that HTLV-I integrates its provirus into random sites in host chromosomal DNA after infection. Clonal integration has been observed in patients with ATLL, including smoldering, chronic and acute leukemia states. Almost all cases with ATLL demonstrate clonal chromosome abnormalities, with karyotypes being very complicated in both number and structure. However, there are no specific karyotype abnormalities in ATLL. In order to examine the role of HTLV-I in the pathogenesis of ATLL, we investigated whether or not HTLV-I randomly integrates and whether the integration site in the human genome is associated with any chromosomal abnormality. We analyzed 18 cases with ATLL, which included 15 cases with acute states, two cases with chronic states and one case with a smoldering state. In four of the 18 cases, the HTLV-I provirus integrated into the 9th chromosome, while in three cases, it integrated into the 1st or 10th chromosome. However, the integrated site in the chromosome varied in each case and the random integration was considered to be true. All 15 cases with acute ATLL had complicated chromosomal abnormalities and two cases with chronic and smoldering ATLL showed simple abnormal karyotypes, while one case with chronic ATLL showed a normal karyotype. In 15 of the 18 cases, the chromosomes with HTLV-I integration showed abnormalities. In particular, in two cases with simple chromosome abnormalities, HTLV-I integrated into the abnormal chromosome, but not into the normal chromosome. The HTLV-I proviral integration thus seems to be associated with chromosome abnormalities. In the multistage leukemogenesis of ATLL, these findings indicate that HTLV-I integration might play an important role in the induction of chromosomal instability.