The Cytochemistry and Morphology Core facilIty comprises three units: a Light Microscopy Unit, an Electron Microscopy Unit, and an image Analysis Unit. This Core Facility is designed to provide accessible, state-of-the art microscopy for funded investigators. A range of services and techniques are provided including routine light photomicroscopy utilizing inverted microscopes or a Zeiss Photoscope III with phase contrast, differential interference contrast, epifluorescence, or interference reflection optics, high resolution immunocytochemistry of 5, 0.5, and 0.1 micromoles frozen sections, either double or single labeled, conventional electron microscopy of plastic sections, In situ hybridization, including labeling of sections with antibodies against protein moieties, scanning confocal microscopy, and image analysis of cells, tissue sections, or photographic negatives using a Zeiss IBAS image analyzer. Drs. Susette Mueller and Wen-Tien Chen are co-directors, and together with the microscopist, Dr. Maozheng Dai, have provided state-of-the-art microscopy instrumentation and expert assistance for studies in tumor cell biology. The instrumentation and personnel have been centralized over the last two years in the Preclinical Science Building. The use of the Core facility has expanded, with the light and image analysis units becoming more heavily utilized. An additional 25% time/effort of the image analysis technician is requested to support an increasingly sophisticated utilization of the Image Analysis Unit. The proposed support for the Image Analysis Technician, Mr. Zitzmann, will allow an increase in powerful image analysis applications tailored for specific research needs. Members from seven programs of the CCSG application, and from nine departments have utilized the Cytochemistry and Morphology Core in the last two years, including work from 23 peer-reviewed funded projects.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA051008-07
Application #
5207614
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
7
Fiscal Year
1996
Total Cost
Indirect Cost
da Cruz, Raquel Santana; Carney, Elissa J; Clarke, Johan et al. (2018) Paternal malnutrition programs breast cancer risk and tumor metabolism in offspring. Breast Cancer Res 20:99
Fan, Ping; Tyagi, Amit K; Agboke, Fadeke A et al. (2018) Modulation of nuclear factor-kappa B activation by the endoplasmic reticulum stress sensor PERK to mediate estrogen-induced apoptosis in breast cancer cells. Cell Death Discov 4:15
Dash, Chiranjeev; Taylor, Teletia R; Makambi, Kepher H et al. (2018) Effect of exercise on metabolic syndrome in black women by family history and predicted risk of breast cancer: The FIERCE Study. Cancer 124:3355-3363
Lynce, Filipa; Blackburn, Matthew J; Cai, Ling et al. (2018) Characteristics and outcomes of breast cancer patients enrolled in the National Cancer Institute Cancer Therapy Evaluation Program sponsored phase I clinical trials. Breast Cancer Res Treat 168:35-41
Paffhausen, Emily S; Alowais, Yasir; Chao, Cara W et al. (2018) Discovery of a stem-like multipotent cell fate. Am J Stem Cells 7:25-37
Lee, Shiao-Pieng; Kao, Chen-Yu; Chang, Shun-Cheng et al. (2018) Tissue distribution and subcellular localizations determine in vivo functional relationship among prostasin, matriptase, HAI-1, and HAI-2 in human skin. PLoS One 13:e0192632
Tiek, D M; Rone, J D; Graham, G T et al. (2018) Alterations in Cell Motility, Proliferation, and Metabolism in Novel Models of Acquired Temozolomide Resistant Glioblastoma. Sci Rep 8:7222
Akinyemiju, Tomi F; Demb, Joshua; Izano, Monika A et al. (2018) The association of early life socioeconomic position on breast cancer incidence and mortality: a systematic review. Int J Public Health 63:787-797
Sehrawat, Archana; Gao, Lina; Wang, Yuliang et al. (2018) LSD1 activates a lethal prostate cancer gene network independently of its demethylase function. Proc Natl Acad Sci U S A 115:E4179-E4188
Furth, Priscilla A (2018) Peroxisome proliferator-activated receptor gamma and BRCA1. Endocr Relat Cancer :

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