Abstract

Introduction. In spite of intensive research during many years, pancreatic adenocarcinoma remains one of the deadliest cancers. The surgical intervention remains main possibility of treatment because chemotherapy and radiotherapy has a minimal impact on long-term survival. We are still looking for the weak points of this devastating disease. Materials and Methods. Pancreatic tumor tissue samples were collected from 36 patients. Immunohistochemistry staining was used to evaluate expression of growth factors and immune infiltrates. Activity of MMP2 and MMP9 was assessed by gelatin zymography on 7.5% SDS-PAGE gel with 0.1% gelatin. Results. All growth factors were strongly expressed in pancreatic tumor tissue. We found that level of expression of c-Met receptor was higher for G3 tumors than for G2 tumors. Also we found that active MMP2 was present at all stages of tumor while active MMP9 just at more advanced tumors. Abundant immune cells infiltration was distinctive for tumor tissue, especially macrophages were infiltrating tumor tissue. We found that amount of macrophages was associated with lymph nodes metastases. Conclusion. In our research we demonstrated that among many factors influencing tumor microenvironment c-Met receptor, infiltrating macrophages and MMP2 have significant influence on development and invasion of pancreatic cancer.

Highlights

  • In spite of intensive research during many years, pancreatic adenocarcinoma remains one of the deadliest cancers

  • The surgical intervention remains main possibility of treatment because chemotherapy and radiotherapy has a minimal impact on long-term survival

  • Pancreatic tumor tissue samples were collected from 36 patients who underwent surgical resection due to pancreatic cancer

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Summary

Introduction

In spite of intensive research during many years, pancreatic adenocarcinoma remains one of the deadliest cancers. In our research we demonstrated that among many factors influencing tumor microenvironment c-Met receptor, infiltrating macrophages and MMP2 have significant influence on development and invasion of pancreatic cancer. Research over the last twenty years has yielded much insight into pancreatic cancer biology, but it has neither improved diagnostics methods nor the way of treatment. It was shown in recent years that the tumor microenvironment plays a critical role in tumor progression [1]. In pancreatic tumors this microenvironment is heterogeneous. It consists of dense fibrotic stroma with cancer cells, stellate cells, infiltrating inflammatory cells, and the remains of the proper structure of the pancreas

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