Xu Tao, Su Bojin, Wang Chunhua, Wang Sumei, Huang Hecheng, Pan Yunbao, Wang Donghui, Wei Weihong, Claret François X, Yang Huiling
Department of Pathophysiology, Zhongshan School of Medicine, Sun Yat-Sen University, Guangdong, Guangzhou 510600, P.R. China.
Department of Radiation Oncology, First People's Hospital of Foshan, Guangdong, Foshan 528000, P.R. China.
Oncol Rep. 2015 Mar;33(3):1418-26. doi: 10.3892/or.2015.3739. Epub 2015 Jan 20.
An important challenge in nasopharyngeal carcinoma (NPC) research is to develop effective predictors of tumor recurrence following treatment to determine whether immediate adjuvant therapy is necessary. We retrospectively analyzed archived specimens collected from 45 patients with paired samples of primary NPC (pNPC) and recurrent NPC (rNPC). Clinical samples were collected from the Cancer Center Databases of the First People's Hospital of Foshan and Shantou Central Hospital (affiliates of Sun Yat-Sen University) between 2001 and 2012. Expression levels of phosphor-Stat3 (p-Stat3), signalosome complex subunit 5 (Jab1/Csn5), Akt1, C/EBP homologous protein (CHOP), Ki-67, and apoptosis were determined by immunohistochemistry in pNPC and rNPC samples from the same patients. Differences in these markers between the short-term interval to recurrence (ITR) group (ITR <18 months) and long-term ITR group (ITR ≥18 months) were further analyzed. In Cox's regression analysis, the ITR was significantly associated as an independent‑negative prognostic factor for overall survival (hazard ratio, 0.211; 95% confidence interval, 0.053-0.841; P=0.027). p-Stat3 was increased in the short-term ITR group (ITR <18 months) and tended to be lower in the long-term ITR group (ITR ≥18 months). In the short-term ITR group, nuclear Akt expression was significantly increased in paired rNPC (P=0.028). In the long-term ITR group, the expression of nuclear Jab1/Csn5 (P=0.047) and assessment of apoptosis measured with TdT-mediated dUTP nick end‑labeling (TUNEL) (P=0.003) was significantly increased in paired rNPC. The results suggest that differences between short- and long-term ITR may predict outcome in rNPC. Furthermore, the overexpression of Jab1/Csn5 and Akt may contribute to the carcinogenesis of rNPC, and Akt seems to promote the progression of short-term ITR. Intra-individual changes of Jab1/Csn5, Akt, and TUNEL may help to identify short-term ITR.
鼻咽癌(NPC)研究中的一项重要挑战是开发有效的治疗后肿瘤复发预测指标,以确定是否有必要立即进行辅助治疗。我们回顾性分析了从45例原发性鼻咽癌(pNPC)和复发性鼻咽癌(rNPC)配对样本患者中收集的存档标本。临床样本于2001年至2012年间从佛山市第一人民医院和汕头市中心医院(中山大学附属医院)的癌症中心数据库中采集。通过免疫组织化学法测定同一患者pNPC和rNPC样本中磷酸化Stat3(p-Stat3)、信号体复合物亚基5(Jab1/Csn5)、Akt1、C/EBP同源蛋白(CHOP)、Ki-67和凋亡的表达水平。进一步分析短期复发间隔(ITR)组(ITR<18个月)和长期ITR组(ITR≥18个月)之间这些标志物的差异。在Cox回归分析中,ITR作为总生存的独立阴性预后因素具有显著相关性(风险比,0.211;95%置信区间,0.053-0.841;P=0.027)。p-Stat3在短期ITR组(ITR<18个月)中升高,而在长期ITR组(ITR≥18个月)中趋于降低。在短期ITR组中,配对rNPC中核Akt表达显著增加(P=0.028)。在长期ITR组中,配对rNPC中核Jab1/Csn5的表达(P=0.047)以及用末端脱氧核苷酸转移酶介导的dUTP缺口末端标记法(TUNEL)检测的凋亡评估(P=0.003)显著增加。结果表明,短期和长期ITR之间的差异可能预测rNPC的预后。此外,Jab1/Csn5和Akt的过表达可能促进rNPC的致癌作用,并且Akt似乎促进短期ITR的进展。Jab1/Csn5、Akt和TUNEL的个体内变化可能有助于识别短期ITR。