Immunoglobulin VH gene analysis in gastric MALT lymphomas

被引:26
|
作者
Sakuma, Hidenori
Nakamura, Tsuneya
Uemura, Naomi
Chiba, Tsutomu
Sugiyama, Toshiro
Asaka, Masahiro
Akamatsu, Taiji
Ueda, Ryuzo
Eimoto, Tadaaki
Goto, Hidemi
Nakamura, Shigeo
Inagaki, Hiroshi [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Pathol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Aichi Canc Ctr Cent Hosp, Dept Endoscopy, Nagoya, Aichi, Japan
[3] Int Med Ctr Japan, Dept Gastroenterol, Tokyo, Japan
[4] Kyoto Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, Kyoto, Japan
[5] Toyama Univ, Grad Sch Med & Pharmaceut Sci, Dept Gastroenterol & Hepatol, Toyama 930, Japan
[6] Hokkaido Univ, Grad Sch Med, Dept Gastroenterol, Sapporo, Hokkaido, Japan
[7] Shinshu Univ Hosp, Dept Endoscopy, Matsumoto, Nagano, Japan
[8] Nagoya City Univ, Grad Sch Med Sci, Dept Internal Med & Mol Sci, Nagoya, Aichi, Japan
[9] Nagoya City Univ, Grad Sch Med, Dept Gastroenterol, Nagoya, Aichi, Japan
[10] Nagoya City Univ, Grad Sch Med, Dept Pathol & Clin Labs, Nagoya, Aichi, Japan
关键词
gastric MALT lymphoma; Helicobacter pylori; eradication; immunoglobulin heavy chain variable genes; API2-MALT1 fusion gene;
D O I
10.1038/modpathol.3800758
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The majority of gastric mucosa-associated lymphoid tissue (MALT) lymphomas are successfully treated with Helicobacter pylori eradication alone. However, certain subsets of these tumors are resistant to the eradication treatment. As API2- MALT1 fusion is a feature of one of these subsets, we divided gastric MALT lymphomas into three groups: eradication-responsive and API2-MALT1 fusion-negative (Group A), eradication-resistant and fusion-negative (Group B), and eradication-resistant and fusion-positive (Group C). To characterize further gastric MALT lymphomas, we analyzed VH genes, which do not change in the course of tumor progression, by extensive subcloning of the monoclonal PCR products of 45 cases. VH3-23 and VH3-30 were preferentially used in Group A tumors (14/23 cases, 61%) as compared with Group B (1/10 cases, 10%, P = 0.0094) and Group C (2/12 cases, 17%, P = 0.017). Tumors of Groups B and C used variegated VH fragments, and no dominant VH fragments were noted. Somatic mutation was detected in most of the cases. Ongoing mutation was detected in 3/45 cases (7%), when assessed according to strict criteria for a confirmed mutation. These findings suggest that inflammation- dependent tumors (Group A) may be derived from a highly restricted, probably H. pylori-associated, B cell subset and may not often progress to those that are inflammation-independent (Groups B and C). Although considered to be common in this tumor, ongoing mutation may be infrequent when assessed by strict criteria.
引用
收藏
页码:460 / 466
页数:7
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