Park Pil-Gu, Jo Su Ji, Kim Min Jung, Kim Hyun Jeong, Lee Ji Hae, Park Cheol Keun, Kim Hyunki, Lee Kang Young, Kim Hoguen, Park Jeon Han, Dong Seung Myung, Lee Jae Myun
Department of Microbiology and Immunology, Yonsei University College of Medicine, Seoul, Republic of Korea.
BK21 PLUS Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea.
Oncotarget. 2017 May 25;8(46):80325-80335. doi: 10.18632/oncotarget.18170. eCollection 2017 Oct 6.
Colorectal cancer (CRC) is one of the most dangerous types of malignant tumors, and cancer metastasis is a major factor in the failure of CRC therapy. Recently, LOXL2 (lysyl oxidase-like 2) has been shown to represent a regulator of epithelial-mesenchymal transition (EMT) in different cancer types. However, LOXL2 has not been reported to be involved in CRC metastasis. In this study, we demonstrated that LOXL2 expression is strongly correlated with the rate of CRC metastasis, it participates in the regulation of EMT-related molecule expression in CRC cells , and it is involved in migratory potential alterations. Additionally, tissue microarray analysis of CRC patients showed an increase in the probability of developing CRC distant metastasis and a decrease in the survival rate of patients with high expression. The results obtained in this study indicate that LOXL2 is involved in the development and progression of CRC metastasis, and therefore, its expression levels may represent a useful prognostic marker.
结直肠癌(CRC)是最危险的恶性肿瘤类型之一,而癌症转移是CRC治疗失败的主要因素。最近,赖氨酰氧化酶样2(LOXL2)已被证明是不同癌症类型中上皮-间质转化(EMT)的调节因子。然而,尚未有报道称LOXL2参与CRC转移。在本研究中,我们证明LOXL2表达与CRC转移率密切相关,它参与CRC细胞中EMT相关分子表达的调节,并参与迁移潜能的改变。此外,对CRC患者的组织芯片分析显示,发生CRC远处转移的概率增加,高表达患者的生存率降低。本研究获得的结果表明,LOXL2参与CRC转移的发生和发展,因此,其表达水平可能是一个有用的预后标志物。