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Effect of preoperative FOLFOX chemotherapy on CCL20/CCR6 expression in colorectal liver metastases
Authors:Rubie Claudia  Frick Vilma Oliveira  Ghadjar Pirus  Wagner Mathias  Justinger Christoph  Graeber Stefan  Sperling Jens  Kollmar Otto  Schilling Martin K
Institution:Claudia Rubie,Vilma Oliveira Frick,Christoph Justinger,Jens Sperling,Otto Kollmar,Martin K Schilling,Department of General,Visceral,Vascular and Paediatric Surgery,University of the Saarland,66421 Homburg/Saar,Germany Pirus Ghadjar,Department of Radiation Oncology,Inselspital,Bern University Hospital and University of Bern,3010 Bern,Switzerland Mathias Wagner,Institute of Pathology,Germany Stefan Graeber,Institute of Medical Biometrics,Epidemiology,and Medical I...
Abstract:AIM: To evaluate the influence of preoperative FOLFOX chemotherapy on CCL20/CCR6 expression in liver metastases of stage IV colorectal cancer (CRC) patients.METHODS: Using Real Time-PCR, enzyme-linked immunosorbent assay, Western Blots and immunohistochemistry, we have analyzed the expression of CCL20, CCR6 and proliferation marker Ki-67 in colorectal liver metastasis (CRLM) specimens from stage IV CRC patients who received preoperative FOLFOX chemotherapy (n = 53) and in patients who did not receive FOLFOX chemotherapy prior to liver surgery (n = 29).RESULTS: Of the 53 patients who received FOLFOX, time to liver surgery was ≤ 1 mo in 14 patients, ≤ 1 year in 22 patients and > 1 year in 17 patients, respectively. In addition, we investigated the proliferation rate of CRC cells in liver metastases in the different patient groups. Both CCL20 and CCR6 mRNA and protein expression levels were significantly increased in patients who received preoperative FOLFOX chemotherapy ≤ 12 mo before liver surgery (P < 0.001) in comparison to patients who did not undergo FOLFOX treatment. Further, proliferation of CRLM cells as measured by Ki-67 was increased in patients who underwent FOLFOX treatment. CCL20 and CCR6 expression levels were significantly increased in CRLM patients who had undergone preoperative FOLFOX chemotherapy.CONCLUSION: This chemokine/receptor up-regulation could lead to increased proliferation/migration through an autocrine mechanism which might be used by surviving metastatic cells to escape cell death caused by FOLFOX.
Keywords:FOLFOX chemotherapy  CCL20/CCR6 expression  Colorectal liver metastases  Proliferation  
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