TY - JOUR
T1 - Emerging clinical importance of the cancer biomarkers kallikrein-related peptidases (KLK) in female and male reproductive organ malignancies
AU - Schmitt, Manfred
AU - Magdolen, Viktor
AU - Yang, Feng
AU - Kiechle, Marion
AU - Bayani, Jane
AU - Yousef, George M.
AU - Scorilas, Andreas
AU - Diamandis, Eleftherios P.
AU - Dorn, Julia
PY - 2013/12
Y1 - 2013/12
N2 - Background. Tumor tissue-associated KLKs (kallikrein-related peptidases) are clinically important biomarkers that may allow prognosis of the cancer disease and/or prediction of response/failure of cancer patients to cancerdirected drugs. Regarding the female/male reproductive tract, remarkably, all of the fifteen KLKs are expressed in the normal prostate, breast, cervix uteri, and the testis, whereas the uterus/endometrium and the ovary are expressing a limited number of KLKs only. Conclusions. Most of the information regarding elevated expression of KLKs in tumor-affected organs is available for ovarian cancer; depicting them as valuable biomarkers in the cancerous phenotype. In contrast, for breast cancer, a series of KLKs was found to be downregulated. However, in breast cancer, KLK4 is elevated which is also true for ovarian and prostate cancer. In such cases, selective synthetic KLK inhibitors that aim at blocking the proteolytic activities of certain KLKs may serve as future candidate therapeutic drugs to interfere with tumor progression and metastasis.
AB - Background. Tumor tissue-associated KLKs (kallikrein-related peptidases) are clinically important biomarkers that may allow prognosis of the cancer disease and/or prediction of response/failure of cancer patients to cancerdirected drugs. Regarding the female/male reproductive tract, remarkably, all of the fifteen KLKs are expressed in the normal prostate, breast, cervix uteri, and the testis, whereas the uterus/endometrium and the ovary are expressing a limited number of KLKs only. Conclusions. Most of the information regarding elevated expression of KLKs in tumor-affected organs is available for ovarian cancer; depicting them as valuable biomarkers in the cancerous phenotype. In contrast, for breast cancer, a series of KLKs was found to be downregulated. However, in breast cancer, KLK4 is elevated which is also true for ovarian and prostate cancer. In such cases, selective synthetic KLK inhibitors that aim at blocking the proteolytic activities of certain KLKs may serve as future candidate therapeutic drugs to interfere with tumor progression and metastasis.
KW - Cancer
KW - Cervix; breast
KW - Endometrium
KW - Ovary
KW - Prostate
KW - Proteases
KW - Testis
KW - Uterus
UR - http://www.scopus.com/inward/record.url?scp=84893806399&partnerID=8YFLogxK
U2 - 10.2478/raon-2013-0053
DO - 10.2478/raon-2013-0053
M3 - Article
AN - SCOPUS:84893806399
SN - 1318-2099
VL - 47
SP - 319
EP - 329
JO - Radiology and Oncology
JF - Radiology and Oncology
IS - 4
ER -