Abstract 91: RalA is frequently up-regulated in human hepatocellular carcinoma and promotes metastasis and cancer stemness

RalA is a Ras-related small GTP binding protein A; however, its functional roles and regulatory mechanisms in hepatocellular carcinoma (HCC) are unclear. In this study, using the RNA-Seq data from TCGA database and our in-house HKU database, we observed that RalA expression was significantly up-regu...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 2018-07, Vol.78 (13_Supplement), p.91-91
Hauptverfasser: Zhao, Luqing, Chan, Lo-Kong, Ho, Daniel Wai-Hung, Tsui, Goofy Yu-Man, Lam, Macrina Wai-Ling, Kam, Charles Shing, Sze, Karen Man-Fong, Zhang, Vanilla Xin, Husain, Abdullah, Lee, Joyce Man-Fong, Ng, Irene Oi-Lin
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Sprache:eng
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Zusammenfassung:RalA is a Ras-related small GTP binding protein A; however, its functional roles and regulatory mechanisms in hepatocellular carcinoma (HCC) are unclear. In this study, using the RNA-Seq data from TCGA database and our in-house HKU database, we observed that RalA expression was significantly up-regulated in human HCCs (P=0.001). This RalA over-expression was validated in a separate cohort of our HCC patients. Upon clinicopathological correlation of RalA in HCC, we found that over-expression of RalA was associated with more aggressive features of HCC patients, with more frequent tumor microsatellite formation (P=0.001), venous invasion (P=0.005) and absence of tumor encapsulation (P=0.005). The over-expression also correlated with poorer overall survival of HCC patients (P
ISSN:0008-5472
1538-7445
DOI:10.1158/1538-7445.AM2018-91