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基质修饰酶赖氨酰氧化酶样 2 在预后不良的侵袭性肝细胞癌中表达增加。

Increased Expression of the Matrix-Modifying Enzyme Lysyl Oxidase-Like 2 in Aggressive Hepatocellular Carcinoma with Poor Prognosis.

机构信息

Department of Pathology, Yonsei University Wonju College of Medicine, Wonju, Korea.

Department of Pathology and Brain Korean PLUS 21 Project for Medical Science, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Gut Liver. 2019 Jan 15;13(1):83-92. doi: 10.5009/gnl17569.

Abstract

BACKGROUND/AIMS: Lysyl oxidase-like 2 (LOXL2), a collagen-modifying enzyme, has been implicated in cancer invasiveness and metastasis.

METHODS

We evaluated the expression of LOXL2 protein, in addition to carbonic anhydrase IX (CAIX), keratin 19, epithelial cell adhesion molecule, and interleukin 6, in 105 resected hepatocellular carcinomas (HCCs) by immunohistochemistry.

RESULTS

LOXL2 positivity was found in 14.3% (15/105) of HCCs, and it was significantly associated with high serum α-fetoprotein levels, poor differentiation, fibrous stroma, portal vein invasion, and advanced TNM stage (p<0.05 for all). Additionally, LOXL2 positivity was significantly associated with CAIX (p=0.005) and stromal interleukin 6 expression (p=0.001). Survival analysis of 99 HCC patients revealed LOXL2 positivity to be a poor prognostic factor; its prognostic impact appeared in progressed HCCs. Furthermore, LOXL2 positivity was shown to be an independent predictor of overall survival and disease-specific survival (p<0.05 for all). Interestingly, co-expression of LOXL2 and CAIX was also an independent predictor for overall survival, disease-specific survival, disease-free survival, and extrahepatic recurrence-free survival (p<0.05 for all).

CONCLUSIONS

LOXL2 expression represents a subgroup of HCCs with more aggressive behavior and is suggested to be a poor prognostic marker in HCC patients.

摘要

背景/目的:赖氨酰氧化酶样蛋白 2(LOXL2)是一种胶原修饰酶,与癌症侵袭和转移有关。

方法

我们通过免疫组织化学方法评估了 105 例切除的肝细胞癌(HCC)中 LOXL2 蛋白的表达,以及碳酸酐酶 9(CAIX)、角蛋白 19、上皮细胞黏附分子和白细胞介素 6 的表达。

结果

LOXL2 阳性在 14.3%(15/105)的 HCC 中发现,与高血清α-胎儿蛋白水平、低分化、纤维基质、门静脉侵犯和晚期 TNM 分期显著相关(所有 p<0.05)。此外,LOXL2 阳性与 CAIX(p=0.005)和间质白细胞介素 6 表达(p=0.001)显著相关。对 99 例 HCC 患者的生存分析显示,LOXL2 阳性是预后不良的因素;其预后影响在进展期 HCC 中表现明显。此外,LOXL2 阳性是总生存率和疾病特异性生存率的独立预测因子(所有 p<0.05)。有趣的是,LOXL2 和 CAIX 的共表达也是总生存率、疾病特异性生存率、无病生存率和肝外无复发生存率的独立预测因子(所有 p<0.05)。

结论

LOXL2 表达代表了具有更具侵袭性行为的 HCC 亚组,并且被认为是 HCC 患者预后不良的标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f77/6347002/2c4a4191d49c/gnl-13-083f1.jpg

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