Oxford Transplant Centre, Churchill Hospital, Oxford, UK.
Pancreas. 2010 Aug;39(6):930-6. doi: 10.1097/MPA.0b013e3181d7abcc.
Focal adhesion kinase (FAK) and Src, 2 protein tyrosine kinases, have been suggested to regulate several fundamental cellular activities that promote the malignant phenotype in various human tumors, including pancreatic adenocarcinoma. Even though research has already turned in laboratory investigations and clinical trials on the possible use of agents blocking the 2 enzymes in cancer management, the data on the clinical significance of FAK and Src in pancreatic adenocarcinoma are still scarce.
The FAK and Src protein expression was assessed immunohistochemically in tumor specimens of 65 patients with pancreatic ductal adenocarcinoma and was statistically analyzed in relation to various clinicopathological characteristics, tumor proliferative capacity, and patients' survival.
The FAK expression correlated significantly with the T stage of the tumor (P = 0.037), whereas FAK staining intensity with patients' age (P = 0.030), tumors' histopathological grade of differentiation (P = 0.041), and M stage (P = 0.029). The Src expression correlated significantly with the stage of the tumor (P = 0.013) and patients' survival (log-rank test, P = 0.027), being also identified as an independent prognostic factor in multivariate analysis (P = 0.047). Furthermore, trends that did not reach statistical significance were noted between FAK and Src expression and staining intensity and several clinicopathological parameters.
The FAK and Src immunohistochemical expression was associated with certain clinicopathological parameters that are crucial for the patients' management.
黏着斑激酶(FAK)和Src 是两种蛋白酪氨酸激酶,它们被认为可以调节多种基本的细胞活动,从而促进各种人类肿瘤(包括胰腺导管腺癌)的恶性表型。尽管已经有研究针对这两种酶在癌症治疗中的潜在应用进行了实验室研究和临床试验,但关于 FAK 和 Src 在胰腺导管腺癌中的临床意义的数据仍然有限。
我们使用免疫组织化学方法检测了 65 例胰腺导管腺癌患者肿瘤标本中的 FAK 和 Src 蛋白表达情况,并对其与各种临床病理特征、肿瘤增殖能力以及患者生存情况之间的关系进行了统计学分析。
FAK 表达与肿瘤的 T 分期显著相关(P = 0.037),而 FAK 染色强度与患者的年龄(P = 0.030)、肿瘤的组织病理学分化程度(P = 0.041)和 M 分期(P = 0.029)相关。Src 表达与肿瘤分期(P = 0.013)和患者生存情况(对数秩检验,P = 0.027)显著相关,并且在多因素分析中也被确定为独立的预后因素(P = 0.047)。此外,还观察到 FAK 和 Src 表达和染色强度与某些临床病理参数之间存在趋势,但未达到统计学意义。
FAK 和 Src 的免疫组织化学表达与对患者管理至关重要的某些临床病理参数相关。