Department of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou 215006, China.
Department of General Surgery, The Second Affiliated Hospital of Soochow University, Suzhou 215006, China.
Biomed Pharmacother. 2017 Oct;94:843-849. doi: 10.1016/j.biopha.2017.07.161. Epub 2017 Aug 10.
Increasing research has indicated that absent in melanoma 2 (AIM2) is aberrantly expressed in several tumor types. However, the association between AIM2 expression and clinicopathological factors or prognosis of patient with colorectal cancer (CRC) remains elusive. In the present study, we first examined the protein and mRNA expression of AIM2 in CRC cell lines by western blotting and quantitative RT-PCR (qRT-PCR). Then, we detected AIM2 expression in CRC tissue using western blotting and immunohistochemistry (IHC) respectively to evaluate its clinicopathological characteristics and prognosis in CRC. Our cytological experiments showed that there was low AIM2 expression in most of the CRC cell lines. Western blotting and IHC indicated that AIM2 expression was obviously lower in the primary CRC tissue than the adjacent normal tissue (P<0.01 and P<0.001). Clinicopathological analysis revealed that low AIM2 expression was significantly associated with some clinicopathological features such as depth of invasion (P=0.020), TNM clinical stage (P=0.013) and lymph node metastasis (P=0.026). Spearman analysis indicated that there was a negative correlation between AIM2 expression and preoperative serum carcino-embryonic antigen (CEA) levels in CRC patients (r=-0.217, P=0.009). Moreover, Kaplan-Meier analysis showed that low expression of AIM2 could lead to a significantly shorter overall survival rate (P=0.001). Cox's proportional hazards model also indicated that the low expression of AIM2 could serve as an independent and significant prognostic factor for survival. Taken together, our findings identify AIM2 as a valuable biomarker for prognosis and a potential therapeutic target for CRC.
越来越多的研究表明,缺失黑色素瘤 2(AIM2)在几种肿瘤类型中异常表达。然而,AIM2 表达与结直肠癌(CRC)患者的临床病理因素或预后之间的关联仍不清楚。在本研究中,我们首先通过 Western blot 和定量 RT-PCR(qRT-PCR)检测了 CRC 细胞系中 AIM2 的蛋白和 mRNA 表达。然后,我们分别通过 Western blot 和免疫组织化学(IHC)检测了 CRC 组织中的 AIM2 表达,以评估其在 CRC 中的临床病理特征和预后。我们的细胞学实验表明,大多数 CRC 细胞系中 AIM2 的表达水平较低。Western blot 和 IHC 表明,AIM2 表达在原发性 CRC 组织中明显低于相邻正常组织(P<0.01 和 P<0.001)。临床病理分析显示,低 AIM2 表达与一些临床病理特征显著相关,如浸润深度(P=0.020)、TNM 临床分期(P=0.013)和淋巴结转移(P=0.026)。Spearman 分析表明,CRC 患者 AIM2 表达与术前血清癌胚抗原(CEA)水平呈负相关(r=-0.217,P=0.009)。此外,Kaplan-Meier 分析显示,AIM2 低表达可导致总生存率显著降低(P=0.001)。Cox 比例风险模型也表明,AIM2 低表达可作为生存的独立且显著的预后因素。综上所述,我们的研究结果表明 AIM2 是预测预后的有价值的生物标志物,也是 CRC 的潜在治疗靶点。