Lasota Jerzy, Miettinen Markku
Department of Soft Tissue Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000, USA.
Semin Diagn Pathol. 2006 May;23(2):91-102. doi: 10.1053/j.semdp.2006.08.006.
Mutually exclusive KIT and PDGFRA mutations are central events in GIST pathogenesis, and their understanding is becoming increasingly important, because specific treatment targeting oncogenic KIT and PDGFRA activation (especially imatinib mesylate) has become available. KIT mutations in GIST are clustered in four exons. Most common are exon 11 (juxtamembrane domain) mutations that include deletions, point mutations (affecting a few codons), and duplications (mostly in the 3' region). The latter mutations most often occur in gastric GISTs. Among gastric GISTs, tumors with deletions are more aggressive than those with point mutations; this does not seem to hold true in small intestinal GISTs. Exon 9 mutations (5-10%) usually are 2-codon 502-503 duplications, and these occur predominantly in intestinal versus gastric GISTs. Lesser imatinib sensitivity of these tumors has been noted. Kinase domain mutations are very rare; GISTs with such mutations are variably sensitive to imatinib. PDGFRA mutations usually occur in gastric GISTs, especially in the epithelioid variants; their overall frequency is approximately 30% to 40% of KIT mutation negative GISTs. Most common is exon 18 mutation leading Asp842Val at the protein level. This mutation causes imatinib resistance. Exon 12 and 14 mutations are rare. Most mutations are somatic (in tumor tissue only), but patients with familial GIST syndrome have consitutitonal KIT/PDGFRA mutations; >10 families have been reported worldwide with mutations generally similar to those in sporadic GISTs. GISTs in neurofibromatosis 1 patients, children, and Carney triad seem to lack GIST-specific KIT and PDGFRA mutations and may have a different disease mechanism. Secondary mutations usually occur in KIT kinase domains in patients after imatinib treatment resulting in resistance to this drug. Mutation genotyping is a tool in GIST diagnosis and in assessment of sensitivity to kinase inhibitors. This is a US government work. There are no restrictions on its use.
互斥的KIT和PDGFRA突变是胃肠道间质瘤(GIST)发病机制的核心事件,随着针对致癌性KIT和PDGFRA激活的特异性治疗(尤其是甲磺酸伊马替尼)的出现,对它们的了解变得越来越重要。GIST中的KIT突变集中在四个外显子中。最常见的是外显子11(近膜结构域)突变,包括缺失、点突变(影响少数密码子)和重复(主要在3'区域)。后一种突变最常发生在胃GIST中。在胃GIST中,有缺失的肿瘤比有点突变的肿瘤更具侵袭性;在小肠GIST中似乎并非如此。外显子9突变(5%-10%)通常是2个密码子502-503的重复,主要发生在小肠GIST而非胃GIST中。已注意到这些肿瘤对伊马替尼的敏感性较低。激酶结构域突变非常罕见;具有此类突变的GIST对伊马替尼的敏感性各不相同。PDGFRA突变通常发生在胃GIST中,尤其是上皮样变体中;它们在KIT突变阴性的GIST中的总体发生率约为30%至40%。最常见的是外显子18突变,在蛋白质水平导致Asp842Val。这种突变导致伊马替尼耐药。外显子12和14突变很少见。大多数突变是体细胞突变(仅在肿瘤组织中),但患有家族性GIST综合征的患者有组成性KIT/PDGFRA突变;全世界已报道超过10个家族有与散发性GIST中通常相似的突变。1型神经纤维瘤病患者、儿童和卡尼三联征中的GIST似乎缺乏GIST特异性的KIT和PDGFRA突变,可能有不同的发病机制。继发性突变通常发生在伊马替尼治疗后的患者的KIT激酶结构域中,导致对该药物耐药。突变基因分型是GIST诊断和评估对激酶抑制剂敏感性的一种工具。这是美国政府的工作。其使用没有限制。