DNA sequence of immunoglobulin heavy chain variable region gene in thyroidlymphoma

Citation
H. Miwa et al., DNA sequence of immunoglobulin heavy chain variable region gene in thyroidlymphoma, JPN J CANC, 92(10), 2001, pp. 1041-1047
Citations number
29
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JAPANESE JOURNAL OF CANCER RESEARCH
ISSN journal
09105050 → ACNP
Volume
92
Issue
10
Year of publication
2001
Pages
1041 - 1047
Database
ISI
SICI code
0910-5050(200110)92:10<1041:DSOIHC>2.0.ZU;2-L
Abstract
Patho-epidemiological studies have shown that thyroid lymphoma (TL) develop s in thyroid affected by chronic lymphocytic thyroiditis (CLTH). CLTH is ca tegorized as an organ-specific autoimmune disease, in which activated B-lym phocytes secrete a number of autoantibodies. Because antigenic stimulation might be involved in the pathogenesis of TL, the variable region in heavy c hain (V-H) genes was characterized in 13 cases with TL and 3 with CLTH. Clo nal rearrangement of the V-H gene was found in 11 cases of TL, and cloning study with sequencing of complimentary determining region (CDR) 3 revealed the presence of a major clone in 4. Three of the 4 cases used V(H)3 gene, w ith the homologous germline gene of V3-30 in two cases and VH26 in one case . A biased usage of V(H)3 and V(H)4 genes with the homologous germline gene of VH26 in V(H)3 gene was reported previously in cases with CLTH. A high l evel of somatic mutation (1-21%, average 12%) with non-random distribution of replacement and silent mutations was accumulated in all cases. The frequ ency of the occurrence of minor clones ranged from 29-44% per case, indicat ing the presence of on-going mutation. DNA sequencing of immunoglobulin V-H gene suggests that TL develops among activated lymphoid cells in CLTH at t he germinal center stage under antigen selection.