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Evaluation of the correlation of vasculogenic mimicry, ALDH1, KAI1 and microvessel density in the prediction of metastasis and prognosis in colorectal carcinoma

机译:评价血管原性模拟,Ald1,Kai1和微血管密度在结直肠癌转移和预后预测中的相关性

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摘要

Abstract Background Metastasis and recurrence are the most common reasons for treatment failure of colorectal carcinoma (CRC). Vasculogenic mimicry (VM, blood supply formation often seen in highly aggressive tumors), Aldehyde dehydrogenase 1 (ALDH1, a biomarker of cancer stem cells), KAI1 (a suppressor gene of tumor metastasis) are all valuable factors for metastasis and prognosis in diverse human cancers. However, the correlation of VM, ALDH1, KAI1 and microvessel density (MVD) in CRC is unclear. In this study, we analyzed the correlations among VM, ALDH1, KAI1 and MVD, as well as their respective correlations with clinicopathological parameters and survival in CRC. Methods The level of VM, ALDH1, KAI1 and MVD in 204 whole tissue samples of CRC were examined by immunhistochemistry. Clinical data was also collected. Results Levels of VM, ALDH1 and MVD were significantly higher, and levels of KAI1 significantly lower, in CRC tissues than in normal colorectal tissues. Levels of VM, ALDH1 and MVD were positively associated with invasion of depth, lymph node metastasis (LNM), distant metastasis and tumor-node-metastasis (TNM) stages, and negatively with patients’ overall survival (OS). Levels of KAI1 was negatively correlated with invasion of depth, LNM, distant metastasis and TNM stages, and the KAI1 positive expression subgroup had significantly longer OS than did the KAI1- subgroup. In multivariate analysis, high levels of VM, ALDH1 and KAI1, as well as TNM stages were independently correlated with lower OS in patients with CRC. Conclusions VM, MVD and the expression of ALDH1 and KAI1 may represent promising metastatic and prognostic biomarkers, as well as potential therapeutic targets for CRC.
机译:摘要背景转移和复发是结直肠癌(CRC)治疗失败的最常见原因。血管原性模拟(VM,血管形成常见于高度侵蚀性肿瘤),醛脱氢酶1(ALDH1,癌症干细胞的生物标志物),KAI1(肿瘤转移的抑制基因)是转移和预后在不同人类中的重要因素癌症。然而,CRC中VM,ALDH1,KAI1和微血管密度(MVD)的相关性尚不清楚。在该研究中,我们分析了VM,AlDH1,Kai1和MVD之间的相关性,以及与CRC中的临床病理参数和存活的各自相关性。方法采用免疫组化检查204例CRC整体组织样品中的VM,ALDH1,KAI1和MVD水平。还收集了临床资料。结果VM,AlDH1和MVD的水平显着高,并且在CRC组织中显着降低的Kai1水平显着降低,而不是正常结肠组织。 VM,AlDH1和MVD的水平与深度,淋巴结转移(LNM),远处转移和肿瘤节点转移(TNM)阶段的侵袭呈正相关,以及对患者的总体存活(OS)负面。 Kai1水平与深度,LNM,远距离转移和TNM阶段的侵袭性呈负相关,并且Kai1阳性表达亚组具有比Kai1-亚组更长的操作系统。在多变量分析中,高水平的VM,AlDH1和Kai1以及TNM阶段与CRC患者的较低OS独立相关。结论VM,MVD和Aldh1和Kai1的表达可以代表有前途的转移性和预后生物标志物,以及CRC的潜在治疗靶标。

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