Document 0325 DOCN M9460325 TI Identification of a common clonal human immunodeficiency virus integration site in human immunodeficiency virus-associated lymphomas. DT 9408 AU Shiramizu B; Herndier BG; McGrath MS; Department of Pediatrics, San Francisco General Hospital,; University of California 94110. SO Cancer Res. 1994 Apr 15;54(8):2069-72. Unique Identifier : AIDSLINE MED/94228518 AB Infection with human immunodeficiency virus type 1 (HIV-1) is associated with a high incidence of lymphoma. Typically, the lymphomas are B-cell in origin, and although they occur in the setting of HIV-1 infection, historical studies have found no evidence for the presence of HIV-1 within the transformed B-cells. We describe a new class of large cell lymphoma wherein HIV p24 expression within the tumor specimens was found to be extremely high. In the first case, HIV was expressed in the tumor-associated transformed T-cells. In three other cases, HIV was found to be highly expressed in tumor-associated macrophages. These tumors exhibited a mixed immunophenotype histologically. Analysis by inverse polymerase chain reaction, using HIV long terminal repeat primers, demonstrated monoclonal HIV integration sites for all four tumors. Direct sequencing of the T-cell lymphoma inverse polymerase chain reaction products identified the HIV integration site within the fur gene, just upstream from the c-fes/fps protooncogene. Using segments of the fur gene as a probe, the other three monoclonal integration sites mapped to the same region. Although the integration and up-regulation of c-fes/fps was localized to the tumor cells within the T-cell lymphoma, the cells containing the monoclonal HIV in the other mixed immunophenotype lymphomas are currently unknown. These observations suggest that HIV may contribute directly to lymphomagenesis and identify a common site of HIV integration within a subset of acquired immunodeficiency syndrome lymphoma. DE Base Sequence DNA Primers Human HIV-1/*GENETICS Immunophenotyping Lymphoma, AIDS-Related/*GENETICS/IMMUNOLOGY/*MICROBIOLOGY/ PATHOLOGY Lymphoma, B-Cell/GENETICS/MICROBIOLOGY/PATHOLOGY Molecular Sequence Data Oligonucleotide Probes Polymerase Chain Reaction Protein-Tyrosine Kinase/GENETICS Proto-Oncogene Proteins/GENETICS *Proto-Oncogenes Restriction Mapping Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. *Virus Integration JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).