Department of Pathology, Keimyung University School of Medicine, Daegu, Korea.
Cancer Res Treat. 2010 Sep;42(3):135-43. doi: 10.4143/crt.2010.42.3.135. Epub 2010 Sep 30.
The purpose of this study was to evaluate the clinicopathological features and immunohistochemical features of gastrointestinal stromal tumor (GIST), and specifically the expressions of platelet derived growth factor receptor A (PDGFRA), protein kinase C theta (PKC theta), discovered on GIST-1 (DOG-1), p16 and p27.
Total 118 patients who underwent surgical resection for GIST at our institution between Jan 1997 and Dec 2007 were retrospectively studied. Immunohistochemical staining for c-kit, PDGFRA, PKC-theta, DOG-1, p16 and p27 was performed on a tissue microarray of the 118 GIST. The clinicopathologic parameters, the disease-free survival (DFS) and the overall survival rate were analyzed along with immunohistochemistry.
The immunohistochemical stains for c-kit, CD34, PKC-theta, PDGFRA, DOG-1, p16 and p27 were positive in 89.8%, 72.0%, 56.8%, 94.9%, 90.7%, 69.5% and 44.1% of the tumor samples, respectively. The immunohistochemical expression of c-kit was strongly correlated with PKC-theta (p=0.000), DOG-1 (p=0.000) and CD34 (p=0.002). The DFS rate was significantly decreased for the patients with peritoneal GIST, high risk GIST, ≥10 cm-sized GIST, ≥10 mitoses/50 high power fields (HPFs) and p16 positivity (p=0.001, p=0.004, p=0.001, p=0.003 and p=0.028). GISTs ≥10 cm, epithelioid tumor cell type, and c-kit, and DOG-1 negativity were significantly associated with shorter period of overall survival (p=0.048, p=0.006, p=0.000 and p=0.000).
The expression of p16 and no expression of c-kit and DOG-1 in GISTs, as well as peritoneal tumor site, high risk group, large tumor size, epithelioid tumor cell type and numerous mitoses, may be potentially prognostic factors for predicting worse outcome for patients who suffer from GIST.
本研究旨在评估胃肠道间质瘤(GIST)的临床病理特征和免疫组织化学特征,特别是血小板衍生生长因子受体 A(PDGFRA)、蛋白激酶 Cθ(PKCθ)、GIST-1(DOG-1)、p16 和 p27 的表达。
回顾性分析 1997 年 1 月至 2007 年 12 月在我院接受手术切除的 118 例 GIST 患者的临床病理参数、无病生存率(DFS)和总生存率,并进行 c-kit、PDGFRA、PKCθ、DOG-1、p16 和 p27 的免疫组织化学染色。
在 118 例 GIST 组织微阵列中,c-kit、CD34、PKCθ、PDGFRA、DOG-1、p16 和 p27 的免疫组织化学染色分别呈阳性 89.8%、72.0%、56.8%、94.9%、90.7%、69.5%和 44.1%。c-kit 的免疫组织化学表达与 PKCθ(p=0.000)、DOG-1(p=0.000)和 CD34(p=0.002)呈强相关。腹膜 GIST、高危 GIST、≥10cm 大小的 GIST、≥10 个有丝分裂/50 高倍视野(HPFs)和 p16 阳性(p=0.001、p=0.004、p=0.001、p=0.003 和 p=0.028)患者的 DFS 率明显降低。GIST 大小≥10cm、上皮样肿瘤细胞类型、c-kit 和 DOG-1 阴性与总生存期缩短显著相关(p=0.048、p=0.006、p=0.000 和 p=0.000)。
GIST 中 p16 的表达以及 c-kit 和 DOG-1 的缺失表达、肿瘤发生部位、高危组、肿瘤较大、上皮样肿瘤细胞类型和有丝分裂较多,可能是预测 GIST 患者预后不良的潜在预后因素。