-Microscopy (MICRO) Shared Resource The Microscopy Shared Resource (MICRO) is a CCSG basic shared resource that combines the expertise and equipment from three different imaging modalities: light microscopy, intravital microscopy and electron microscopy. This combination gives LCCC members access to outstanding imaging capabilities. Visualization of the process of oncogenesis from tumors in whole organs, to cancer cells invading normal tissues, to transformed cells growing in culture and finally visualization of the macromolecules which lie at the heart of transformation provides a critical means of understanding, manipulating, and ultimately combating cancer. Having a broad range of imaging tools immediately available to the cancer research community at UNC within the LCCC is essential if the diverse research of the many cutting edge studies are to progress rapidly toward their goals in cancer research. This requires specialized techniques spanning a range of visualization that encompasses light and electron microscopy and dimensions of millimeters to nanometers. To provide this technology to the LCCC members, three highly specialized laboratories work together and each has an excellent history of accomplishments. The three components of the LCCC Microscopy SR consist of: The Microscopy Services Laboratory (MSL) which stands as the main supplier of widefield, confocal, and live cell imaging plus image analysis and morphometry. The Intravital Imaging SR provides a unique set of microscopes and expertise for imaging cells, tissues and organs within a living animal. The Electron Microscopy SR provides specialized imaging techniques for macromolecular imaging that have been developed by the SR director and are used world wide. Taken together, these three SRs provide a powerful tool for our cancer researchers. Future directions include expansion of light microscopy into the realm of super-resolution imaging and establishment of new methods for tagging specific proteins such that they can be localized in cells by high resolution thin sectioning.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA016086-44
Application #
9834849
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2019-12-01
Budget End
2020-11-30
Support Year
44
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Lim, Joseph K; Liapakis, Ann Marie; Shiffman, Mitchell L et al. (2018) Safety and Effectiveness of Ledipasvir and Sofosbuvir, With or Without Ribavirin, in Treatment-Experienced Patients With Genotype 1 Hepatitis C Virus Infection and Cirrhosis. Clin Gastroenterol Hepatol 16:1811-1819.e4
Wang, Gary P; Terrault, Norah; Reeves, Jacqueline D et al. (2018) Prevalence and impact of baseline resistance-associated substitutions on the efficacy of ledipasvir/sofosbuvir or simeprevir/sofosbuvir against GT1 HCV infection. Sci Rep 8:3199
Phillips, Bonnie; Van Rompay, Koen K A; Rodriguez-Nieves, Jennifer et al. (2018) Adjuvant-Dependent Enhancement of HIV Env-Specific Antibody Responses in Infant Rhesus Macaques. J Virol 92:
Lianga, Noel; Doré, Carole; Kennedy, Erin K et al. (2018) Cdk1 phosphorylation of Esp1/Separase functions with PP2A and Slk19 to regulate pericentric Cohesin and anaphase onset. PLoS Genet 14:e1007029
Allott, Emma H; Geradts, Joseph; Cohen, Stephanie M et al. (2018) Frequency of breast cancer subtypes among African American women in the AMBER consortium. Breast Cancer Res 20:12
Dhungel, Bal Mukunda; Montgomery, Nathan D; Painschab, Matthew S et al. (2018) 'Discovering' primary effusion lymphoma in Malawi. AIDS 32:2264-2266
Cameron, Jennifer E; Rositch, Anne F; Vielot, Nadja A et al. (2018) Epstein-Barr Virus, High-Risk Human Papillomavirus and Abnormal Cervical Cytology in a Prospective Cohort of African Female Sex Workers. Sex Transm Dis 45:666-672
Dronamraju, Raghuvar; Jha, Deepak Kumar; Eser, Umut et al. (2018) Set2 methyltransferase facilitates cell cycle progression by maintaining transcriptional fidelity. Nucleic Acids Res 46:1331-1344
Koehler, Jennifer W; Miller, Andrew D; Miller, C Ryan et al. (2018) A Revised Diagnostic Classification of Canine Glioma: Towards Validation of the Canine Glioma Patient as a Naturally Occurring Preclinical Model for Human Glioma. J Neuropathol Exp Neurol 77:1039-1054
Takaku, Motoki; Grimm, Sara A; Roberts, John D et al. (2018) GATA3 zinc finger 2 mutations reprogram the breast cancer transcriptional network. Nat Commun 9:1059

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