Emerging roles of proteases in tumour suppression
By C. López‐Otín, L. Matrisian. Nature Reviews. Cancer, 2007
826 citations recorded by the source corpus.
Subfields: Cancer Research, Hematology, Oncology
View Paper: https://www.semanticscholar.org/paper/154aee3278a145ccfc7f04b0521f1fdc6024a1a3
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Citations in the corpus
- Matrix Metalloproteinases: Regulators of the Tumor Microenvironment (2010, background): “The tumor-suppressing functions of these MMPs is probably another reason for the failure of broad-spectrum MPIs as anticancer drugs (Lopez-Otin and Matrisian, 2007).”
- The metastatic niche: adapting the foreign soil (2009, background): “MMPs are instrumental in degrading ECM components during inflammatory responses and tissue repair as well as in primary tumour growt”
- Metalloproteinase‐dependent and ‐independent processes contribute to inhibition of breast cancer cell migration, angiogenesis and liver metastasis by a disintegrin and metalloproteinase with thrombospondin motifs‐15 (2015, background): “Also ADAMTS1 is among several ADAMTS genes that are epigenetically silenced in many types of cancer suggesting its function as a tumor-suppressor.(1,29) How then can we rationalize this apparent duality? The ADAMTS enzymes are ECM-binding proteases whose substrates include integral matrix components”
- Higher sensitivity of Adamts12-deficient mice to tumor growth and angiogenesis (2010, positive): “Recently, the generation of animal models involving gain or loss of function of matrix metalloproteinases (MMPs) has led to the surprising discovery of tumor-suppressive function for some proteases (Lopez-Otin and Matrisian, 2007).”
- Lysosomal membrane permeabilization in cell death (2008, background): “In addition to these tumor-promoting effects of cathepsins, evidence is emerging that proteases, and in particular cathepsins, may have a function as tumor suppressors as well (Lopez-Otin and Matrisian, 2007).”
- The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin motifs) family (2015, background): “For many family members, the dominant theme is tumor suppression as they show epigenetic silencing (ADAMTS1, 8, 9, 12 and 18) or mutational inactivation (ADAMTS15) in several cancer types [48, 51, 108–114].”