This Section has focused on the role of Ca++ as a regulator of gene expression and cellularphysiology. Using CAI as a tool, we have investigated Ca++-regulated molecular events. A novel gene, CAIR-1, was cloned from CAI conditioned cells. Studies over the past year have investigated the signal transduction function of CAIR-1 and were initiated to identify a function for CAIR-1. We have demonstrated by cellular fractionation and immunohistochemistry that CAIR-1 is a cytosolic protein that is found broadly within the cell by confocal immunofluorescence. CAIR-1 is expressed in vascular tissue and epithelial cells of multiple tumor types with no clear difference yet defined between tumor and normal cells; there is minimal expression in stroma. It is present in the epithelial cells of ovarian carcinoma specimens and stains their small vessels as well. A borderline ovarian cancer specimen also showed limited staining for CAIR-1. Staining was also seen in kidney cancer, breast cancer, and colon cancer specimens. Cohorts are now being assembled to determine if CAIR-1 expression by cellular localization or relative quantity may be a marker for malignancy or aggressiveness. Pre- and post- CAI treatment specimens will be obtained in the current phase II CAI clinical trial and will be tested for changes in CAIR-1 expression by immunohistochemistry and/or RT-PCR. CAIR-1 function studies are being driven by putative functional domains in the protein. The PXXP regions suggest that CAIR-1 should bind SH3-containing proteins. Our hypothesis that CAIR-1 should function downstream of a calcium-regulated or calcium-associated pathways led to the identification of phospholipase C-gamma (PLC-g) as a putative partner protein. Coimmunoprecipitation studies indicate that CAIR-1 binds to PLC-g under basal conditions and is dissociated when cells are stimulated with epidermal growth factor. Transfection studies have begun directed at expression of full length CAIR-1 and its putative domains, as potential dominant negative constructs. These transfectants will be analyzed for functional status and alterations in calcium related signal transduction. - signal transduction, calcium, phospholipase C,

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01SC009163-12
Application #
6290799
Study Section
Special Emphasis Panel (LP)
Project Start
Project End
Budget Start
Budget End
Support Year
12
Fiscal Year
1999
Total Cost
Indirect Cost
Name
National Cancer Institute Division of Clinical Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Rasool, Nabila; LaRochelle, William; Zhong, Haihong et al. (2010) Secretory leukocyte protease inhibitor antagonizes paclitaxel in ovarian cancer cells. Clin Cancer Res 16:600-9
Kassis, Jareer N; Virador, Victoria M; Guancial, Elizabeth A et al. (2009) Genomic and phenotypic analysis reveals a key role for CCN1 (CYR61) in BAG3-modulated adhesion and invasion. J Pathol 218:495-504
Virador, Victoria M; Davidson, Ben; Czechowicz, Josephine et al. (2009) The anti-apoptotic activity of BAG3 is restricted by caspases and the proteasome. PLoS One 4:e5136
Elstrand, Mari Bunkholt; Kleinberg, Lilach; Kohn, Elise C et al. (2009) Expression and clinical role of antiapoptotic proteins of the bag, heat shock, and Bcl-2 families in effusions, primary tumors, and solid metastases in ovarian carcinoma. Int J Gynecol Pathol 28:211-21
Gunn, Andrew J; Hama, Yukihiro; Koyama, Yoshinori et al. (2007) Targeted optical fluorescence imaging of human ovarian adenocarcinoma using a galactosyl serum albumin-conjugated fluorophore. Cancer Sci 98:1727-33
Davidson, Ben; Espina, Virginia; Steinberg, Seth M et al. (2006) Proteomic analysis of malignant ovarian cancer effusions as a tool for biologic and prognostic profiling. Clin Cancer Res 12:791-9
Kassis, Jareer N; Guancial, Elizabeth A; Doong, Howard et al. (2006) CAIR-1/BAG-3 modulates cell adhesion and migration by downregulating activity of focal adhesion proteins. Exp Cell Res 312:2962-71
Kassis, Jareer; Klominek, Julius; Kohn, Elise C (2005) Tumor microenvironment: what can effusions teach us? Diagn Cytopathol 33:316-9
Kamrava, Mitchell; Simpkins, Fiona; Alejandro, Emilyn et al. (2005) Lysophosphatidic acid and endothelin-induced proliferation of ovarian cancer cell lines is mitigated by neutralization of granulin-epithelin precursor (GEP), a prosurvival factor for ovarian cancer. Oncogene 24:7084-93
Perabo, Frank G E; Demant, Andre W; Wirger, Andreas et al. (2005) Carboxyamido-triazole (CAI) reverses the balance between proliferation and apoptosis in a rat bladder cancer model. Anticancer Res 25:725-9

Showing the most recent 10 out of 22 publications