Department of Oncology, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
PLoS One. 2013 May 24;8(5):e63854. doi: 10.1371/journal.pone.0063854. Print 2013.
β-catenin plays a key role in the progression of colorectal cancer (CRC). However, its prognostic significance for patients with CRC remains controversial.
Identical search strategies were used to search relevant literatures in the PubMed, Embase and Web of Science databases. The correlation between β-catenin expression and clinicopathological features and prognosis was analyzed.
A total of 18 studies met the inclusion criteria, which comprised 3665 cases. Meta-analysis suggested that β-catenin overexpression in the nucleus was significantly associated with disease free survival (DFS) (n = 541 in 3 studies; HR = 1.87, 95% CI: 1.28-2.71; Z = 3.26; P = 0.001) and overall survival (OS) for CRC patients (n = 2630 in 10 studies; HR = 1.55, 95% CI: 1.12-2.14; Z = 2.62; P = 0.009). However, there was no significant association between β-catenin expression in the cytoplasm and OS (n = 1327 in 3 studies; HR = 1.04, 95% CI: 0.88-1.24, Z = 0.46, P = 0.643). The combined odds ratio (OR) of β-catenin in the nucleus indicated that β-catenin overexpression was associated with advanced stage CRC (n = 950 in 7 studies; OR = 0.71, 95% CI: 0.53-0.94; Z = 2.35; P = 0.019) and metastasis of CRC (n = 628 in 5 studies; OR = 0.49, 95% CI: 0.25-0.96, Z = 2.06, P = 0.039). β-catenin overexpression in the nucleus had no correlation with the tumor site (colon or rectum), differentiation grade, lymph node status or depth of invasion. The pooled ORs were 1.09 (95% CI: 0.41-2.91, Z = 0.18, P = 0.856), 1.27(95% CI: 0.76-2.10, Z = 0.92, P = 0.357), 0.71(95% CI: 0.46-1.09, Z = 1.58, P = 0.115) and 0.82(95% CI: 0.4-1.68, Z = 0.53, P = 0.594).
This study showed that β-catenin overexpression in the nucleus, rather than in the cytoplasm, appeared to be associated with progress disease and a worse prognosis for CRC patients.
β-连环蛋白在结直肠癌(CRC)的进展中起关键作用。然而,其对 CRC 患者的预后意义仍存在争议。
采用相同的搜索策略,在 PubMed、Embase 和 Web of Science 数据库中搜索相关文献。分析β-连环蛋白表达与临床病理特征和预后的相关性。
共有 18 项研究符合纳入标准,共纳入 3665 例患者。荟萃分析表明,β-连环蛋白核内过表达与无病生存(DFS)显著相关(3 项研究中 541 例;HR=1.87,95%CI:1.28-2.71;Z=3.26;P=0.001)和 CRC 患者的总生存(OS)(10 项研究中 2630 例;HR=1.55,95%CI:1.12-2.14;Z=2.62;P=0.009)。然而,β-连环蛋白在细胞质中的表达与 OS 无显著相关性(3 项研究中 1327 例;HR=1.04,95%CI:0.88-1.24,Z=0.46,P=0.643)。核内β-连环蛋白的联合优势比(OR)表明,β-连环蛋白过表达与 CRC 的晚期阶段(7 项研究中 950 例;OR=0.71,95%CI:0.53-0.94;Z=2.35;P=0.019)和 CRC 的转移(5 项研究中 628 例;OR=0.49,95%CI:0.25-0.96,Z=2.06,P=0.039)相关。β-连环蛋白核内过表达与肿瘤部位(结肠或直肠)、分化程度、淋巴结状态或浸润深度无关。汇总 OR 分别为 1.09(95%CI:0.41-2.91,Z=0.18,P=0.856)、1.27(95%CI:0.76-2.10,Z=0.92,P=0.357)、0.71(95%CI:0.46-1.09,Z=1.58,P=0.115)和 0.82(95%CI:0.4-1.68,Z=0.53,P=0.594)。
本研究表明,β-连环蛋白核内过表达,而非细胞质内过表达,似乎与 CRC 患者的疾病进展和预后不良有关。