Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chun W. Tam"'
Publikováno v:
Journal of Pineal Research. 54:69-79
Our laboratory has recently demonstrated a melatonin MT1 receptor-mediated antiproliferative signaling mechanism in androgen receptor (AR)-positive prostate epithelial cells which involves up-regulation of p27(Kip1) through dual activation of Gα(s)/
Publikováno v:
Journal of Pineal Research. 49:301-311
Melatonin has been shown to inhibit the proliferation of malignant and transformed human prostate epithelial cells by transcriptional up-regulation of p27(Kip1) expression via MTNR1A receptor-mediated activation of protein kinase A (PKA) and protein
Publikováno v:
Endocrinology. 147:5023-5033
A possible role of the PDZ domain-containing protein 2 (PDZD2) in prostate tumorigenesis has been suggested. Besides, PDZD2 is posttranslationally cleaved by a caspasedependent mechanism to form a secreted PDZ domaincontaining protein 2 (sPDZD2) with
Autor:
Chun W. Tam, Stephen Y. W. Shiu
Publikováno v:
Journal of pineal research. 51(3)
Recently, a novel melatonin MT(1) receptor-mediated antiproliferative signaling mechanism involving transcriptional up-regulation of p27(Kip1) due to paralleled stimulation of protein kinase A (PKA) and protein kinase C (PKC), as a result of respecti
Publikováno v:
Journal of pineal research. 49(3)
Melatonin has been shown to inhibit the proliferation of malignant and transformed human prostate epithelial cells by transcriptional up-regulation of p27(Kip1) expression via MTNR1A receptor-mediated activation of protein kinase A (PKA) and protein
Publikováno v:
Journal of pineal research. 45(4)
Circannual variation in the human serum levels of prostate-specific antigen, a growth marker of the prostate gland, has been reported recently. The present study was conducted to investigate the role of the photoperiodic hormone melatonin (MLT) and i
Publikováno v:
Journal of pineal research. 42(2)
There is an unmet clinical demand for safe and effective pharmaceuticals/nutraceuticals for prostate cancer prevention and hormone-refractory prostate cancer treatment. Previous laboratory and human studies of our laboratory demonstrated an associati