Knight Cancer Institute, Oregon Health and Science University Portland, Oregon ; Division of Hematology and Oncology, Oregon Health and Science University Portland, Oregon.
Cancer Med. 2013 Feb;2(1):21-31. doi: 10.1002/cam4.57. Epub 2013 Feb 3.
Gastrointestinal stromal tumors (GISTs) arise from the interstitial cells of Cajal (ICCs) and are the most common mesenchymal neoplasm of the gastrointestinal tract. While the majority of GISTs harbor activating mutations in either the v-kit Hardy-Zuckerman feline sarcoma viral oncogene homolog (KIT) or platelet-derived growth factor receptor alpha (PDGFRA) tyrosine kinases, approximately 10-15% of adult GISTs and 85% of pediatric GISTs lack such mutations. These "wild-type" GISTs have been reported to express high levels of the insulin-like growth factor 1 receptor (IGF1R), and IGF1R-targeted therapy of wild-type GISTs is being evaluated in clinical trials. However, it is not clear that all wild-type GISTs express IGF1R, because studies to date have predominantly focused on a particular subtype of gastric wild-type GIST that is deficient in the mitochondrial succinate dehydrogenase (SDH) complex. This study of a series of 136 GISTs, including 72 wild-type specimens, was therefore undertaken to further characterize wild-type GIST subtypes based on the relative expression of transcripts encoding IGF1R. Additional transcripts relevant to GIST biology were also evaluated, including members of the IGF-signaling pathway (IGF1, IGF2, and insulin receptor [INSR]), neural markers (CDH2[CDH: Cadherin], neurofilament, light polypeptide, LHX2 [LHX: LIM homeobox], and KIRREL3 [KIRREL: kin of IRRE like]), KIT, PDGFRA, CD34, and HIF1A. Succinate dehydrogenase complex, subunit B protein expression was also assessed as a measure of SDH complex integrity. In addition to the previously described SDH-deficient, IGF1R(high) wild-type GISTs, other SDH-intact wild-type subpopulations were defined by high relative expression of IGF1R, neural markers, IGF1 and INSR, or low IGF1R coupled with high IGF2. These results underscore the complexity and heterogeneity of wild-type GISTs that will need to be factored into molecularly-targeted therapeutic strategies.
胃肠道间质瘤(GISTs)起源于 Cajal 间质细胞(ICCs),是胃肠道最常见的间叶性肿瘤。虽然大多数 GIST 存在 v-kit Hardy-Zuckerman 猫肉瘤病毒致癌基因同源物(KIT)或血小板衍生生长因子受体 alpha(PDGFRA)酪氨酸激酶的激活突变,但约 10-15%的成人 GIST 和 85%的儿童 GIST 缺乏此类突变。这些“野生型”GIST 已被报道表达高水平的胰岛素样生长因子 1 受体(IGF1R),并且正在临床试验中评估针对野生型 GIST 的 IGF1R 靶向治疗。然而,并非所有野生型 GIST 都表达 IGF1R 尚不清楚,因为迄今为止的研究主要集中在一种特定的胃野生型 GIST 亚型上,该亚型缺乏线粒体琥珀酸脱氢酶(SDH)复合物。因此,这项对包括 72 例野生型标本在内的 136 例 GIST 的研究旨在进一步根据编码 IGF1R 的转录本的相对表达来表征野生型 GIST 亚型。还评估了与 GIST 生物学相关的其他转录本,包括 IGF 信号通路(IGF1、IGF2 和胰岛素受体 [INSR])、神经标记物(CDH2[CDH:钙粘蛋白]、神经丝、轻多肽、LHX2 [LHX:LIM 同源盒]和 KIRREL3 [KIRREL:IRRE 样类似物])、KIT、PDGFRA、CD34 和 HIF1A。还评估了琥珀酸脱氢酶复合物亚单位 B 蛋白的表达,作为 SDH 复合物完整性的衡量标准。除了先前描述的 SDH 缺陷、IGF1R(高)野生型 GIST 之外,还通过高相对表达 IGF1R、神经标记物、IGF1 和 INSR 或低 IGF1R 结合高 IGF2 定义了其他 SDH 完整的野生型亚群。这些结果强调了野生型 GIST 的复杂性和异质性,这将需要纳入分子靶向治疗策略。