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Matrix-Degrading Type II Transmembrane Serine Protease Matriptase: Its Role in Cancer Development and Malignancy

並列摘要


Proteolysis on the cell surface has well-known roles in the tissue homeostasis and in the pathogenesis such as cancers. A newly described, epithelia-derived type II transmembrane serine protease, matriptase, has been shown with important roles in the epithelial homeostasis, i.e., terminal keratinocyte differentiation, as well as its deregulation in the cancer development and progression. In epithelia, matriptase has a cognate inhibitor HAI-1 (hepatocyte growth factor activator inhibitor-1) for the regulation of this protease expression, trafficking, and activity. In animal model, matriptase is essential for postnatal survival, epidermal barrier function, stratum corneum, and hair follicle development, as well as thymocyte survival. Deregulated matriptase induces carcinogenesis and malignant transformation. In human cancers, both matriptase and HAI-1 expression are recurrently lost of their balance, resulting in activation of the protease, which is correlated with clinical stages. Thus, malfunction of matriptase potently raises cancer development and metastatic cancer lesions.

並列關鍵字

matriptase HAI-1 serine protease protease inhibitor

被引用紀錄


Liao, Y. Z. (2015). 間質蛋白酶在表皮生長因子與K-Ras所誘發之大腸癌細胞侵襲移動能力中扮演角色 [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2015.02417
Ko, C. J. (2015). 第二型嵌膜絲胺酸蛋白酶II在攝護腺癌症進程及轉移所扮演的角色 [doctoral dissertation, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2015.02384
Hsia, Y. H. (2015). 草藥萃取物NTU04及MSL-UH抑制胰腺癌侵襲力以及機制之研究 [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2015.00615
Hsieh, H. Y. (2014). 探討嵌膜蛋白酶在人類大腸上皮細胞間緊密連接形成過程中扮演的角色 [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2014.00380
Lin, H. Y. (2012). 探討第二型間質蛋白酶在人類攝護腺癌細胞轉移中所扮演的角色 [master's thesis, National Taiwan University]. Airiti Library. https://doi.org/10.6342/NTU.2012.01954

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