Gan Xiaoning, Lin Xiaomiao, He Rongquan, Lin Xinggu, Wang Hanlin, Yan Liyan, Zhou Hong, Qin Hui, Chen Gang
Department of Pathology, First Affiliated Hospital of Guangxi Medical University, Nanning, Guangxi Zhuang Autonomous Region 530021, China.
Department of Children Rehabilitation Medicine, Guangxi Maternal and Child Health Hospital, 225 Xinyang Road, Nanning, Guangxi Zhuang Autonomous Region 530003, China.
Dis Markers. 2016;2016:5259602. doi: 10.1155/2016/5259602. Epub 2016 Apr 20.
p16, encoded by the CDKN2A gene, is a tumor suppressor that has been widely studied in cancer research. However, the relationship of p16 with prognostic and clinicopathological parameters in patients with bladder cancer remains unclear. Data inclusion criteria were articles reporting on the relationship between p16 expression and the prognosis or clinicopathology in patients with bladder cancer. Meta-analyses were performed with Stata software. Hazard ratios (HRs) or odds ratios (ORs) and 95% confidence intervals (95% CI) were calculated to evaluate the relative risks. The source of heterogeneity was analyzed by subgroup analysis. A total of 37 studies with 2246 cases were included and analyzed. The results identified an important link between downregulated p16 expression and poor prognosis in patients with bladder cancer in terms of recurrence-free survival (RFS), overall survival (OS), progression-free survival (PFS), and some clinicopathological parameters including clinical staging, pathological degree, and lymph node metastasis. Subgroup analysis also showed that low p16 expression could function as a warning sign for RFS and PFS in patients with early-stage (Ta-T1) bladder cancer. In conclusion, p16 might play an essential role in the deterioration of bladder cancer and could serve as a biomarker for the prediction for patients' progression and prognosis.
由CDKN2A基因编码的p16是一种肿瘤抑制因子,在癌症研究中已得到广泛研究。然而,p16与膀胱癌患者的预后及临床病理参数之间的关系仍不清楚。数据纳入标准为报道p16表达与膀胱癌患者预后或临床病理之间关系的文章。使用Stata软件进行荟萃分析。计算风险比(HRs)或优势比(ORs)以及95%置信区间(95%CI)以评估相对风险。通过亚组分析来分析异质性来源。共纳入并分析了37项研究,涉及2246例病例。结果表明,就无复发生存期(RFS)、总生存期(OS)、无进展生存期(PFS)以及包括临床分期、病理分级和淋巴结转移在内的一些临床病理参数而言,p16表达下调与膀胱癌患者预后不良之间存在重要关联。亚组分析还显示,低p16表达可作为早期(Ta-T1)膀胱癌患者RFS和PFS的警示信号。总之,p16可能在膀胱癌恶化过程中起重要作用,并可作为预测患者病情进展和预后的生物标志物。