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
相关论文
共 50 条
  • [31] Immunoglobulin VH Gene Analysis of Splenic Marginal Zone Lymphoma Histologic Variants
    Bahler, D. W.
    Szankasi, P.
    Dufresne, S. D.
    Felgar, R. E.
    Swerdlow, S. H.
    LABORATORY INVESTIGATION, 2009, 89 : 254A - 255A
  • [32] Immunoglobulin VH Gene Analysis of Splenic Marginal Zone Lymphoma Histologic Variants
    Bahler, D. W.
    Szankasi, P.
    Dufrense, S. D.
    Felgar, R. E.
    Swerdlow, S. H.
    MODERN PATHOLOGY, 2009, 22 : 254A - 255A
  • [33] PCR for immunoglobulin gene rearrangement detects residual MALT lymphoma in histologically negative gastric biopsies
    Ahrens, William
    Sklar, Jeffrey
    Jain, Dhanpat
    Patriub, Vytas
    Lagarde, Sue
    Robert, Marie
    GASTROENTEROLOGY, 2006, 130 (04) : A526 - A526
  • [34] Evaluation of microsat, ellite instability in gastric MALT lymphomas.
    Siakantaris, Marina P.
    Angelopoulou, Maria K.
    Lilakos, Konstantinos
    Metaxas, Yannis
    Moschoyianni, Maria
    Gamaletsou, Maria
    Vassilakopoulos, Theodoros P.
    Kyrtsonis, Marie-Christine
    Korkolopoulou, Penelope
    Panayiotidis, Panayiotis
    Pangalis, Gerassimos A.
    BLOOD, 2006, 108 (11) : 237B - 237B
  • [35] Update of the role of surgery in the multimodal treatment of MALT gastric lymphomas
    Kelessis, NG
    Vassilopoulos, PP
    Bai, MP
    Agnantis, NJ
    Avital, SR
    Rosenthal, RJ
    ANTICANCER RESEARCH, 2002, 22 (6B) : 3457 - 3463
  • [36] A (Lympho)cyte to See: Simultaneous Gastric and Pulmonary MALT Lymphomas
    Whealdon, J.
    Demirci, T.
    Benes, L.
    Basavaraj, A.
    Hena, K.
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2022, 205
  • [37] GASTRIC MALT LYMPHOMAS AND RESPONSE TO HELICOBACTER PYLORI ERADICATION THERAPY
    Noa Pedroso, G.
    de Oca Megias, E. Montes
    Gutierrez Carrillo, B.
    Mas Paez, J. A.
    Perez Menendez, R.
    Mulet Hernandez, H.
    Dominguez Alvarez, C.
    HELICOBACTER, 2013, 18 : 154 - 154
  • [38] Microsatellite instability in gastric MALT lymphomas and other associated neoplasms
    Furlan, D
    Bertoni, F
    Cerutti, R
    Taborelli, M
    Pinotti, G
    Roggero, E
    Cavalli, F
    Bonato, M
    Zucca, E
    Capella, C
    ANNALS OF ONCOLOGY, 1999, 10 (07) : 783 - 788
  • [39] Gastric MALT lymphomas, new insight and still unanswered questions
    Zucca, E
    Roggero, E
    Cavalli, F
    ITALIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 1998, 30 (01): : 5 - 9
  • [40] Chromosomal abnormalities in gastric MALT lymphomas predictive for malignant progression
    Toracchio, Sonia
    Luca, James
    Peterson, Leif
    Ota, Hiroyoshi
    Katsuyama, Tsutomu
    Rugge, Massimo
    Graham, David
    El-Zimaity, Maha M. T.
    El-Zimaity, Hala M.
    GASTROENTEROLOGY, 2007, 132 (04) : A619 - A619