Isaacson P G, Du M Q
Department of Histopathology, University College London, UK.
Verh Dtsch Ges Pathol. 2003;87:116-22.
Gastric mucosa associated lymphoid tissue (MALT) lymphoma is a histologically distinct tumour derived from MALT acquired as a result of Helicobacter pylori infection. Eradication of H. pylori causes clinical regression of the lymphoma n 75 % of cases. In seeking to identify those cases resistant to this therapy, and in the interests of further understanding the biology of MALT lymphoma, genetic alterations of MALT lymphomas have been investigated. Three translocations, t(11;18)(q21; q21), t(1;14)(p22;q32) and t(14;18)(q32;q21) are specifically associated with MALT lymphoma and the genes involved have been identified. T(11;18) results in a chimeric fusion between the API2 and MALT1 genes and is specifically associated with gastric MALT lymphomas that do not respond to eradication of H. pylori. T(1; 14) and t(14; 18) deregulate bcl-10 and MALT1 expression respectively. These three chromosomal translocations that involve different genes appear to share common oncogenic properties by targeting the to target the same NFkappaB oncogenic pathway.
胃黏膜相关淋巴组织(MALT)淋巴瘤是一种组织学上独特的肿瘤,源于幽门螺杆菌感染导致的获得性MALT。根除幽门螺杆菌可使75%的淋巴瘤病例出现临床缓解。为了确定那些对该疗法耐药的病例,并进一步了解MALT淋巴瘤的生物学特性,人们对MALT淋巴瘤的基因改变进行了研究。三种易位,即t(11;18)(q21;q21)、t(1;14)(p22;q32)和t(14;18)(q32;q21)与MALT淋巴瘤特异性相关,且相关基因已被确定。T(11;18)导致API2和MALT1基因之间发生嵌合融合,与对根除幽门螺杆菌无反应的胃MALT淋巴瘤特异性相关。T(1;14)和t(14;18)分别使bcl-10和MALT1表达失调。这三种涉及不同基因的染色体易位似乎通过靶向相同的NFκB致癌途径而具有共同的致癌特性。