TY - JOUR
T1 - Role of imbalance between neutrophil elastase and α1-antitrypsin in cancer development and progression
AU - Sun, Zhifu
AU - Yang, Ping
N1 - Funding Information:
We thank Susan Ernst for her technical assistance with the manuscript This work was supported by grant no. NIH-CA80127 (Yang) from the US National Cancer Institute and Mayo Foundation Funds
PY - 2004/3/1
Y1 - 2004/3/1
N2 - Neutrophil elastase and α1-antitrypsin are a pair of protease and protease inhibitor counterparts. The imbalance between the two counterparts is generally thought to cause tissue damage, which could create a favourable tissue environment for carcinogens and tumour progression. Laboratory research and clinical findings have indicated that a deficiency in α1-antitrypsin is associated with increased risk of liver cancer, bladder cancer, gall bladder cancer, malignant lymphoma, and lung cancer. Conversely, raised concentrations of neutrophil elastase might promote the development, invasion, and metastasis of many cancers. Several mechanisms of carcinogenesis have been postulated. Excess neutrophil elastase might facilitate cancer development by causing tissue damage and air trapping, which foster longer carcinogen exposure, might promote cancer progression by degrading the intercellular matrix barrier, and might directly lead to cancer development through the tumour-necrosis-factor signalling pathway.
AB - Neutrophil elastase and α1-antitrypsin are a pair of protease and protease inhibitor counterparts. The imbalance between the two counterparts is generally thought to cause tissue damage, which could create a favourable tissue environment for carcinogens and tumour progression. Laboratory research and clinical findings have indicated that a deficiency in α1-antitrypsin is associated with increased risk of liver cancer, bladder cancer, gall bladder cancer, malignant lymphoma, and lung cancer. Conversely, raised concentrations of neutrophil elastase might promote the development, invasion, and metastasis of many cancers. Several mechanisms of carcinogenesis have been postulated. Excess neutrophil elastase might facilitate cancer development by causing tissue damage and air trapping, which foster longer carcinogen exposure, might promote cancer progression by degrading the intercellular matrix barrier, and might directly lead to cancer development through the tumour-necrosis-factor signalling pathway.
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U2 - 10.1016/S1470-2045(04)01414-7
DO - 10.1016/S1470-2045(04)01414-7
M3 - Review article
C2 - 15003202
AN - SCOPUS:1342287837
SN - 1470-2045
VL - 5
SP - 182
EP - 190
JO - The Lancet Oncology
JF - The Lancet Oncology
IS - 3
ER -