Chen H, Hirota S, Isozaki K, Sun H, Ohashi A, Kinoshita K, O'Brien P, Kapusta L, Dardick I, Obayashi T, Okazaki T, Shinomura Y, Matsuzawa Y, Kitamura Y
Department of Internal Medicine and Molecular Science, Graduate School of Medicine Osaka University, Osaka, Japan.
Gut. 2002 Dec;51(6):793-6. doi: 10.1136/gut.51.6.793.
Diffuse proliferation of interstitial cells of Cajal (ICCs) in the myenteric plexus layer of the intestine has been described in patients with familial and multiple gastrointestinal stromal tumours (GISTs). However, it is not fully understood whether proliferation is polyclonal or monoclonal.
To evaluate the clonal nature of diffuse ICC proliferation in familial and multiple GIST cases, we carried out clonal analysis using inactivation at the human androgen receptor (HUMARA) locus.
Diffuse ICC proliferation tissues from three female patients were microdissected using a laser capture microdissection (LCM) system. Normal intestinal mucosal tissues were also microdissected for polyclonal controls and GIST tissues for monoclonal controls from the same patients, and genomic DNA was extracted. After digestion by restriction enzyme HhaI, the HUMARA locus was amplified by a fluorescent polymerase chain reaction (PCR) procedure and the PCR products were analysed.
One case was uninformative because it was homozygous at the HUMARA locus. In the two other cases, PCR products from the diffuse ICC proliferation showed two alleles as well as those from normal intestinal mucosal tissues, indicating that ICC proliferation was polyclonal. In contrast, PCR products from associated GIST tissues showed only one allele, indicating that GISTs were monoclonal.
The results suggested that diffuse ICC proliferation in familial and multiple GIST cases was non-neoplastic hyperplasia.
在患有家族性和多发性胃肠道间质瘤(GIST)的患者中,已观察到肠肌间神经丛层中 Cajal 间质细胞(ICC)的弥漫性增殖。然而,目前尚不完全清楚这种增殖是多克隆性还是单克隆性的。
为了评估家族性和多发性 GIST 病例中弥漫性 ICC 增殖的克隆性质,我们利用人类雄激素受体(HUMARA)基因座的失活进行了克隆分析。
使用激光捕获显微切割(LCM)系统对 3 名女性患者的弥漫性 ICC 增殖组织进行显微切割。还对同一患者的正常肠黏膜组织进行显微切割作为多克隆对照,对 GIST 组织进行显微切割作为单克隆对照,并提取基因组 DNA。用限制性内切酶 HhaI 消化后,通过荧光聚合酶链反应(PCR)程序扩增 HUMARA 基因座,并对 PCR 产物进行分析。
1 例因 HUMARA 基因座纯合而无法提供信息。在另外 2 例中,弥漫性 ICC 增殖的 PCR 产物与正常肠黏膜组织的 PCR 产物一样显示出两个等位基因,表明 ICC 增殖是多克隆性的。相比之下,相关 GIST 组织的 PCR 产物仅显示一个等位基因,表明 GIST 是单克隆性的。
结果表明,家族性和多发性 GIST 病例中的弥漫性 ICC 增殖是非肿瘤性增生。