TY - JOUR
T1 - Tumor-Stroma Interaction of Human Pancreatic Cancer
T2 - Acquired Resistance to Anticancer Drugs and Proliferation Regulation Is Dependent on Extracellular Matrix Proteins
AU - Miyamoto, Hidenori
AU - Murakami, Tatsuya
AU - Tsuchida, Kunihiro
AU - Sugino, Hiromu
AU - Miyake, Hidenori
AU - Tashiro, Seiki
PY - 2004/1
Y1 - 2004/1
N2 - Introduction: Pancreatic cancer is one of the major causes of cancer-related deaths in industrialized countries. It is known that pancreatic cancer is resistant to chemotherapy and that cancer cells are surrounded by extracellular matrix (ECM) proteins including collagen 1, collagen IV, fibronectin, and laminin. Aims: To examine the role of ECM proteins in acquired resistance to anticancer drugs and proliferation regulation in pancreatic cancers. Methodology and Results: We used an in vitro model of ECM-induced chemoresistance and cell proliferation of cancer, cell lines (M1A PaCa-2, PANC-1, and Capan-1) with 3 different malignancy grades and found that resistance to cytotoxic drugs and proliferation regulation was dependent on ECM proteins. Pancreatic cancer cell lines, especially M1A PaCa-2 cells, adhering to any of the ECM proteins showed decreased cytotoxicity of anticancer drugs, except for gemcitabine. PANC-1 and Capan-1 cells adhering to fibronectin, collagen I, and collagen IV proliferated more than the controls. Conclusion: ECM proteins have important roles in acquired resistance to anticancer drugs and cell proliferation regulation of pancreatic cancer cells. Therefore, the expression of ECM proteins in pancreatic cancer specimens could provide valuable information to aid anticancer drug cytotoxicity, and gemcitabine would be useful for treatment of patients with pancreatic cancer.
AB - Introduction: Pancreatic cancer is one of the major causes of cancer-related deaths in industrialized countries. It is known that pancreatic cancer is resistant to chemotherapy and that cancer cells are surrounded by extracellular matrix (ECM) proteins including collagen 1, collagen IV, fibronectin, and laminin. Aims: To examine the role of ECM proteins in acquired resistance to anticancer drugs and proliferation regulation in pancreatic cancers. Methodology and Results: We used an in vitro model of ECM-induced chemoresistance and cell proliferation of cancer, cell lines (M1A PaCa-2, PANC-1, and Capan-1) with 3 different malignancy grades and found that resistance to cytotoxic drugs and proliferation regulation was dependent on ECM proteins. Pancreatic cancer cell lines, especially M1A PaCa-2 cells, adhering to any of the ECM proteins showed decreased cytotoxicity of anticancer drugs, except for gemcitabine. PANC-1 and Capan-1 cells adhering to fibronectin, collagen I, and collagen IV proliferated more than the controls. Conclusion: ECM proteins have important roles in acquired resistance to anticancer drugs and cell proliferation regulation of pancreatic cancer cells. Therefore, the expression of ECM proteins in pancreatic cancer specimens could provide valuable information to aid anticancer drug cytotoxicity, and gemcitabine would be useful for treatment of patients with pancreatic cancer.
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U2 - 10.1097/00006676-200401000-00006
DO - 10.1097/00006676-200401000-00006
M3 - Article
C2 - 14707728
AN - SCOPUS:0346157370
SN - 0885-3177
VL - 28
SP - 38
EP - 44
JO - Pancreas
JF - Pancreas
IS - 1
ER -
