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DOI 10.1186/1477-7819-12-231

Медицинская библиотека · World journal of surgical oncology · 2014

Expression levels of insulin-like growth factors and receptors in hepatocellular carcinoma: a retrospective study.

Chun Yun Shin, Huang Min, Rink Lori, Von Mehren Margaret

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

BACKGROUND

The insulin-like growth factor (IGF) pathway is implicated in the pathogenesis of hepatocellular carcinoma (HCC) and may be important in nonalcoholic fatty liver disease (NAFLD). The aim of this study is to determine expression levels of IGFs and receptors in NAFLD-associated HCC.

METHODS

Tissue microarrays were constructed from patients who underwent hepatectomy for HCC. Immunohistochemistry was performed using antibodies for IGF ligands and receptors. Immunostain results were scored by a pathologist blinded to clinical data.

RESULTS

Among 27 patients with HCC, the most common underlying liver diseases included NAFLD, hepatitis C, and alcoholic hepatitis. Expression levels of IGFs and receptors were not associated with patients' underlying liver disease. In all patients, IGF-2 expression was upregulated in tumor and adjacent non-neoplastic liver. Expression of IGF-1 was low in adjacent liver in 6 of 10 patients with cirrhosis, compared with 2 of 17 patients without cirrhosis (P = 0.025). Higher IGF-1 expression in liver adjacent to tumor was associated with poorer median survival of 22 months, compared with 72 months with equal or lower IGF-1 expression in adjacent liver relative to tumor (P = 0.006).

CONCLUSIONS

Our preliminary results demonstrate significant associations between IGF-1 expression and liver cirrhosis and survival after resection in patients with HCC, independent of their underlying liver disease.

Для цитирования: Chun Yun Shin, Huang Min, Rink Lori, Von Mehren Margaret. Expression levels of insulin-like growth factors and receptors in hepatocellular carcinoma: a retrospective study.. World journal of surgical oncology. 2014. DOI: 10.1186/1477-7819-12-231.

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