I Department of Otolaryngology and Laryngological Oncology, Medical University of Łódź, Kopcińskiego 22, 90-153, Łódź, Poland.
Department of Cytobiochemistry, University of Łódź, Pomorska 142/143, 90-236, Łódź, Poland.
Cell Oncol (Dordr). 2018 Jun;41(3):253-268. doi: 10.1007/s13402-017-0367-z. Epub 2018 Jan 3.
Aberrant fibroblast growth factor receptor (FGFR) expression is thought to contribute to the development of many types of cancer. As yet, however, their impact on the course and prognosis of head and neck cancer remains to be determined. Here, we aimed to investigate the effects of expression of the FGFR family members FGFR1 and FGFR3, as well as their downstream PI3K/AKT signal-regulated kinases, on the aggressiveness and prognosis of laryngeal cancer.
In total 137 surgically removed squamous cell laryngeal cancer (SCLC) and 100 matched non-cancerous laryngeal mucosa (NCLM) samples were assessed for mRNA expression using quantitative real-time PCR. The corresponding proteins were analyzed by Western blotting. SLUG expression was assessed by immunohistochemistry. The expression data were subsequently related to tumor front grading (TFG), local/nodal recurrences, prognosis and overall survival.
The FGFR1, FGFR3 and PI3K/AKT kinase mRNA and protein levels were found to be significantly higher in the SCLC than the NCLM samples (p < 0.05). A high FGFR1 mRNA/protein expression level was found to be associated with an increased invasion rate, according to TFG scale and SLUG level, a high local/nodal recurrence rate and a poor prognosis (p < 0.05). Similarly, we found that a high FGFR3 mRNA/protein expression level was associated with a shorter survival time (p < 0.05). In addition, we found that high PI3K/AKT kinase mRNA/protein levels were associated with a high TFG (p < 0.05). We also found that FGFR1/3 mRNA and FGFR1 protein levels were inversely associated with overall survival (log-rank test: FGFR1 mRNA p = 0.03, FGFR3 mRNA p = 0.04, FGFR1 protein p = 0.03). Subsequent multivariate analyses revealed that high FGFR3 mRNA expression may serve as an independent poor prognostic factor (HR 2.32, 95% CI 1.03-6.59; p = 0.04). We also found that the p-PI3K regulatory kinase protein level was significantly associated with survival in the cohort studied (HR 1.78, 95% CI 0.64-8.53; p = 0.03).
From our data we conclude that FGFR1 and FGFR3, as well as its downstream regulatory PI3K/AKT kinases, may serve as potential biomarkers for the invasiveness and prognosis of laryngeal cancer. The expression of FGFR1/3-PI3K/AKT regulatory pathway members may be instrumental for the identification of patients at risk for an unfavorable clinical outcome.
异常成纤维细胞生长因子受体(FGFR)的表达被认为是许多类型癌症发展的原因。然而,它们对头颈部癌症的病程和预后的影响仍有待确定。在这里,我们旨在研究 FGFR 家族成员 FGFR1 和 FGFR3 及其下游 PI3K/AKT 信号调节激酶的表达对喉癌侵袭性和预后的影响。
使用定量实时 PCR 检测 137 例手术切除的鳞状细胞喉癌(SCLC)和 100 例匹配的非癌性喉黏膜(NCLM)样本中的 mRNA 表达。通过 Western blot 分析相应的蛋白质。通过免疫组织化学评估 SLUG 表达。随后将表达数据与肿瘤前缘分级(TFG)、局部/淋巴结复发、预后和总生存期相关联。
与 NCLM 样本相比,SCLC 中的 FGFR1、FGFR3 和 PI3K/AKT 激酶 mRNA 和蛋白水平明显升高(p<0.05)。根据 TFG 量表和 SLUG 水平,高 FGFR1 mRNA/蛋白表达水平与侵袭率增加、局部/淋巴结复发率高和预后不良相关(p<0.05)。同样,我们发现高 FGFR3 mRNA/蛋白表达水平与较短的生存时间相关(p<0.05)。此外,我们发现高 PI3K/AKT 激酶 mRNA/蛋白水平与 TFG 高相关(p<0.05)。我们还发现 FGFR1/3 mRNA 和 FGFR1 蛋白水平与总生存期呈负相关(对数秩检验:FGFR1 mRNA p=0.03,FGFR3 mRNA p=0.04,FGFR1 蛋白 p=0.03)。随后的多变量分析表明,高 FGFR3 mRNA 表达可能是独立的不良预后因素(HR 2.32,95%CI 1.03-6.59;p=0.04)。我们还发现,研究队列中 p-PI3K 调节激酶蛋白水平与生存显著相关(HR 1.78,95%CI 0.64-8.53;p=0.03)。
从我们的数据中可以得出结论,FGFR1 和 FGFR3 及其下游调节 PI3K/AKT 激酶可能是喉癌侵袭性和预后的潜在生物标志物。FGFR1/3-PI3K/AKT 调节途径成员的表达可能有助于识别具有不利临床结局风险的患者。