Abstract:
Background: The effect of proteolytic enzymes including Cathepsin K (CatK), a cysteine
cathepsin, in onset and progression of cancers including apoptosis, proliferation, cancer
immunology, inflammatory cell recruitment to tumors and aiding in the mobilization of normal
healthy cells from their tissue compartments assisting in cancers and their metastasis in human
has been research intensive. CatK involves in various aspects and stages of cancer and
metastasis.
Objective: To collect together and summarize biochemical and physiological pathways of how
CatK is involved in metastasis of breast and prostate cancers and CatK regulated mechanisms
underlying metastasis of such cancers to bones.
Methodology: Information for the review was gathered through published literature from global
databases including Google Scholar and PUBMED through nearly 50 different studies done on
investigating physiological and biochemical interactions between enzymatic activity of CatK
with breast and prostate cancers and their metastasis to bones. Keywords used were prostate and
breast cancers, CatK, enzymatic activity, physiology and biochemistry.
Results: Analysis of published studies revealed that immunohistochemical studies of breast
cancer cells indicate that they over express CatK resulting in induction of wrong mechanisms of
cell signaling in breast cancers, creating a higher tendency for their metastasis to bones.
Immunohistochemical, immunoprecipitation and fluorgenic assays of prostste cancers indicated
elevated levels of CatK. Lesions derived from prostate cancer cell masses were observed to
undergo increased bone formation and resorption levels. Such resorption levels causes secretion
of biological factors promoting tumor expansion. CatK was observed to be a key component
promoting higher resorption levels.
Conclusions: It is concluded that CatK is over expressed in breast and prostate cancers and this
over expression triggers cancer inducing biomolecules to cause metastais of them to bones.
Authors suggest that, to completely understand the association of CatK on cancerous cells and
their mechanism in metastasis, distributory patterns of CatK in human tissues needs to be
extensively studied.
