下调和上调
癌症研究
转移
运动性
肿瘤进展
细胞生长
细胞
癌
原发性肿瘤
癌症
生物
医学
病理
内科学
细胞生物学
基因
生物化学
遗传学
作者
Ying-Hui Zhu,Haibo Liu,Li-Yi Zhang,Tingting Zeng,Ye Song,Yanru Qin,Lei Li,Lulu Liu,Jianbiao Li,Baozhu Zhang,Xin‐Yuan Guan
出处
期刊:Carcinogenesis
[Oxford University Press]
日期:2014-02-07
卷期号:35 (5): 1154-1161
被引量:10
标识
DOI:10.1093/carcin/bgu040
摘要
Here, we report the characterization of a candidate tumor suppressor gene leucine-rich glioma inactivated 1 (LGI1) in human esophageal squamous cell carcinoma (ESCC). Downregulation of LGI1 has been detected in approximately 50% of primary ESCCs, which was significantly associated with advanced clinical stage (P < 0.001), lymph node metastasis (P < 0.001), tumor invasion (P = 0.009) and poor disease-specific survival (P < 0.001). Functional studies found that LGI1 could inhibit cell growth, clonogenicity, cell motility and tumor formation in nude mice. Mechanistic investigations suggested that LGI1 acted through extracellular signal-regulated kinase (ERK1/2) signaling to downregulate matrix metalloproteinase (MMP)-3 expression and subsequently suppressed tumor metastasis. Taken together, our study revealed that LGI1 plays an important tumor suppressive role in the development and progression of ESCC, with possible application in clinics as a biomarker and a potential new therapeutic target.
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