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TRAIL expression levels in human hepatocellular carcinoma have implications for tumor growth, recurrence and survival
Author(s) -
PirasStraub Katja,
Khairzada Khaleda,
Trippler Martin,
Baba Hideo A.,
Kaiser Gernot M.,
Paul Andreas,
Canbay Ali,
Weber Frank,
Gerken Guido,
Herzer Kerstin
Publication year - 2014
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.29139
Subject(s) - hepatocellular carcinoma , hccs , liver transplantation , medicine , apoptosis , liver cancer , liver disease , pathology , immunohistochemistry , tumor necrosis factor alpha , cancer , cancer research , carcinoma , transplantation , oncology , biology , biochemistry
The proapoptotic molecule TNF‐related apoptosis‐inducing ligand (TRAIL) has earned attention because of its ability to induce apoptosis in liver cancer cells without damaging normal liver cells. It may play an important role in preventing the development and outgrowth of hepatocellular carcinoma (HCC). TRAIL expression was investigated in a large series of human HCCs. We analyzed liver tissue from 108 patients undergoing partial liver resection (PLR) or liver transplantation (LT) because of either HCC or other indications. TRAIL expression was correlated with the cause of liver disease, demographic and clinical variables and pathologic properties. Our analysis found that in 66% of HCCs TRAIL expression was significantly lower than in the surrounding non‐cancerous liver tissue ( p ≤ 0.012). Separation by cause of disease showed that HCC TRAIL mRNA expression was lower in almost all groups than in non‐cancerous tissue but most significantly lower in NASH‐associated liver tumors. Interestingly, low HCC TRAIL expression was found to correlate with tumor size ( p ≤ 0.007) and stage, as well as with tumor recurrence after resection and poor survival rates. The results of this study suggest that low TRAIL mRNA levels may be both a dominant feature in HCC development and growth and a predictor of tumor recurrence and poorer survival rates.