Subject(s)
Carcinoma, Adenosquamous/pathology , Hepatectomy/methods , Liver Neoplasms/pathology , Liver/pathology , Neoplasm Recurrence, Local/pathology , Aged , Antigens, Tumor-Associated, Carbohydrate/genetics , Biomarkers, Tumor/genetics , Carcinoembryonic Antigen/genetics , Carcinoma, Adenosquamous/diagnostic imaging , Carcinoma, Adenosquamous/genetics , Carcinoma, Adenosquamous/surgery , Fatal Outcome , Female , Gene Expression , Humans , Keratin-5/genetics , Keratin-6/genetics , Liver/diagnostic imaging , Liver/metabolism , Liver/surgery , Liver Neoplasms/diagnostic imaging , Liver Neoplasms/genetics , Liver Neoplasms/surgery , Neoplasm Recurrence, Local/diagnostic imaging , Neoplasm Recurrence, Local/genetics , Neoplasm Recurrence, Local/surgery , Tomography, X-Ray ComputedABSTRACT
Colorectal cancer (CRC) is one of the most aggressive tumours in the human digestive system. Most CRC patients have poor prognosis due to metastasis and recurrence. Angiopoietin-like 4 (ANGPTL4) is involved in tumour development. Regulatory T (Treg) cells and M2 macrophages promote tumour growth and metastasis. Herein, we explored the changes of ANGPTL4 expression in CRC patients at different stages and observed whether in situ tumour-Treg and -M2 macrophages are correlated with ANGPTL4 expression. Serum ANGPTL4 (sANGPTL4) levels of 70 CRC patients and 10 healthy controls were detected by ELISA. ANGPTL4, Foxp3 and CD163 expression levels in CRC tissues were measured by immunohistochemistry. Recombinant ANGPTL4 (rANGPTL4) proteins were further added into cell-culture systems for induction of Treg cells and M2 macrophages. The results showed both sANGPTL4 and in situ tumour-ANGPTL4 expression levels increased in Dukes C-D stage CRC patients. Foxp3+ and CD163+ cells in tumour tissue sections were also more intensive in Dukes C-D stage patients than in Dukes A-B stage patients. Foxp3+ and CD163+ cells in tumour tissues were positively correlated with both tissue and sANGPTL4 expression (P < 0.01). Recombinant ANGPTL4 promoted the induction of murine Treg cells and M2 macrophages ex vivo. Therefore, elevated ANGPTL4 expression could be a marker for advanced CRC. Treg cell and M2 macrophage induction could be one of the mechanisms of tumour promotion mediated by ANGPTL4.
