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Elevated levels of Ser/Thr protein phosphatase 5 (PP5) in human breast cancer.
- Source :
-
Biochimica et biophysica acta [Biochim Biophys Acta] 2008 Apr; Vol. 1782 (4), pp. 259-70. Date of Electronic Publication: 2008 Jan 26. - Publication Year :
- 2008
-
Abstract
- Ser/Thr protein phosphatase 5 (PP5) regulates several signaling-cascades that suppress growth and/or facilitate apoptosis in response to genomic stress. The expression of PP5 is responsive to hypoxia inducible factor-1 (HIF-1) and estrogen, which have both been linked to the progression of human breast cancer. Still, it is not clear if PP5 plays a role in the development of human cancer. Here, immunostaining of breast cancer tissue-microarrays (TMAs) revealed a positive correlation between PP5 over-expression and ductal carcinoma in situ (DCIS; P value 0.0028), invasive ductal carcinoma (IDC; P value 0.012) and IDC with metastases at the time of diagnosis (P value 0.0001). In a mouse xenograft model, the constitutive over-expression of PP5 was associated with an increase in the rate of tumor growth. In a MCF-7 cell culture model over-expression correlated with both an increase in the rate of proliferation and protection from cell death induced by oxidative stress, UVC-irradiation, adriamycin, and vinblastine. PP5 over-expression had no apparent effect on the sensitivity of MCF-7 cells to taxol or rapamycin. Western analysis of extracts from cells over-expressing PP5 revealed a decrease in the phosphorylation of known substrates for PP5. Together, these studies indicate that elevated levels of PP5 protein occur in human breast cancer and suggest that PP5 over-expression may aid tumor progression.
- Subjects :
- Animals
Cell Death
Cell Line, Tumor
Doxorubicin pharmacology
Humans
Mice
Mice, Nude
Nuclear Proteins
Oxidative Stress
Phosphoprotein Phosphatases
Threonine
Time Factors
Ultraviolet Rays
Up-Regulation
Vinblastine pharmacology
Breast Neoplasms enzymology
Carcinoma, Ductal, Breast enzymology
Carcinoma, Intraductal, Noninfiltrating enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 0006-3002
- Volume :
- 1782
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Biochimica et biophysica acta
- Publication Type :
- Academic Journal
- Accession number :
- 18280813
- Full Text :
- https://doi.org/10.1016/j.bbadis.2008.01.004