Mastitis is a common infection ofthe breast during lactation. Mastitis is either infective or due to milk stasis and induces inflammation in the extracellular matrix or stroma of the breast. Mastitis resolves with treatment but causes involution of mammary lobules. Episodes of mastitis are known to increase the risk of breast cancer. Moreover, in the post-lactation period, the breast cancer risk is increased, independent of mastitis. This is in part due to the induction of inflammatory genes during the process of involution. This project aims to determine if breast cancer develops more readily in a post-mastitis milieu. Using high-throughput technologies, we aim to define the acute and chronic changes that mastitis induces in the extracellular matrix (stroma) and how these changes contribute to the formation of breast cancer. Lastly, we aim to define the effects of mastitis on PTHrP signaling in the mammary stroma and PTHrP's role in promoting breast cancer via its effects on mammary stem cells. As a Junior Investigator in the COBRE in Matrix Biology, I will work with my scientific mentor to complete the scientific aims and to develop a grant proposal for future R01 funding.

Public Health Relevance

): Breast cancer progression is worsened by both inflammation and the stiffness of the extracellular matrix. Successful completion ofthe proposed aims will result in an improved understanding ofthe forces driving breast cancer progression, and the identification of potential therapeutic targets.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Exploratory Grants (P20)
Project #
5P20GM109095-03
Application #
9067406
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2016-06-01
Budget End
2017-05-31
Support Year
3
Fiscal Year
2016
Total Cost
Indirect Cost
Name
Boise State University
Department
Type
DUNS #
072995848
City
Boise
State
ID
Country
United States
Zip Code
83725
Beard Jr, Richard S; Hoettels, Brian A; Meegan, Jamie E et al. (2018) AKT2 maintains brain endothelial claudin-5 expression and selective activation of IR/AKT2/FOXO1-signaling reverses barrier dysfunction. J Cereb Blood Flow Metab :271678X18817512
Yocham, Katie M; Scott, Crystal; Fujimoto, Kiyo et al. (2018) Mechanical Properties of Graphene Foam and Graphene Foam - Tissue Composites. Adv Eng Mater 20:
Browning, Landon; Patel, Megha R; Horvath, Eli Bring et al. (2018) IL-6 and ovarian cancer: inflammatory cytokines in promotion of metastasis. Cancer Manag Res 10:6685-6693
Anwar, Mehruba; Turner, Matthew; Farrell, Natalija et al. (2018) Hikers poisoned: Veratrum steroidal alkaloid toxicity following ingestion of foraged Veratrum parviflorum. Clin Toxicol (Phila) 56:841-845
Rohn, Troy T; Mack, Jacob M (2018) Apolipoprotein E Fragmentation within Lewy Bodies of the Human Parkinson's Disease Brain. Int J Neurodegener Dis 1:
Pandhi, Twinkle; Kreit, Eric; Aga, Roberto et al. (2018) Electrical Transport and Power Dissipation in Aerosol-Jet-Printed Graphene Interconnects. Sci Rep 8:10842
Misra, N; Wines, T F; Knopp, C L et al. (2018) Immunogenicity of a Staphylococcus aureus-cholera toxin A2/B vaccine for bovine mastitis. Vaccine 36:3513-3521
Thompson, William R; Yen, Sherwin S; Uzer, Gunes et al. (2018) LARG GEF and ARHGAP18 orchestrate RhoA activity to control mesenchymal stem cell lineage. Bone 107:172-180
Misra, N; Pu, X; Holt, D N et al. (2018) Immunoproteomics to identify Staphylococcus aureus antigens expressed in bovine milk during mastitis. J Dairy Sci 101:6296-6309
Graham, David M; Andersen, Tomas; Sharek, Lisa et al. (2018) Enucleated cells reveal differential roles of the nucleus in cell migration, polarity, and mechanotransduction. J Cell Biol 217:895-914

Showing the most recent 10 out of 87 publications