Metastasis is responsible for the majority of cancer deaths despite progress in cancer treatment over the past decades. The PI3K signaling pathway, which is mutated at high frequencies in various forms of human cancers, has been implicated in the metastatic process, but the cellular mechanism is poorly understood. Recent studies into the fundamental mechanism of cell migration open up new opportunities to investigate how cancer cells migrate and metastasize. Using Dictyostelium and human neutrophils as models, the principle investigator (PI) has demonstrated that cell migration depends on the coupling between an excitable Ras-PI3K network and a cytoskeletal network to drive the formation of protrusions. The objectives of this proposal are (1) to assess to what extent a similar coupling between an excitable PI3K signaling network and a cytoskeletal network drives the migration of cancer cells; (2) to investigate how altered PI3K signaling activity affect the dynamics of the molecular networks to change the motility and metastatic behavior of cancer cells. To achieve these objectives, the PI will use cutting edge imaging techniques to visualize the spatiotemporal dynamics of various signaling and cytoskeletal activities in breast cancer cells to understand the features and functions of these activities (Aim 1). The PI3K signaling activity will be altered using genetic or pharmacological methods to study how the signaling and cytoskeletal activities are affected, and how these changes affect the migration of cells in vitro (Aim 2). The dynamics of the molecular networks in various cancer cells with or without altered Pi3K signaling will then be correlated with their ability to metastasize in mice (Aim 3). Finally, the PI3K signaling and cytoskeletal activities will be examined in primary and metastatic tumors from breast cancer patients to confirm the clinical relevance of experimental findings (Aim 4). The successful completion of these aims will provide valuable information for developing molecular interventions for metastatic cancers. The PI has received clinical training prior to his research career. The award will support the PI to obtain preliminary results required for independent funding and acquire new skills through collaboration, particularly regarding the use of mice and patient samples. The long-term goal of the PI is to apply fundamental cell biology to the development of new interventions for cancers.

Public Health Relevance

Despite tremendous progress in cancer treatment, metastasis remains the major cause of death in cancer patients. Recent progress in the fundamental biology of cell movement provides an opportunity to understand how genetic mutations in the molecular networks cause cancer cells to metastasize and may reveal more effective strategies to control the metastatic process.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Career Transition Award (K22)
Project #
5K22CA212060-03
Application #
9654615
Study Section
Subcommittee I - Transistion to Independence (NCI)
Program Officer
Korczak, Jeannette F
Project Start
2017-04-01
Project End
2020-03-31
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
3
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Pathology
Type
Schools of Medicine
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Yang, J-Ming; Bhattacharya, Sayak; West-Foyle, Hoku et al. (2018) Integrating chemical and mechanical signals through dynamic coupling between cellular protrusions and pulsed ERK activation. Nat Commun 9:4673
Yu, Yu; Suryo Rahmanto, Yohan; Lee, Meng-Horng et al. (2018) Inhibition of ovarian tumor cell invasiveness by targeting SYK in the tyrosine kinase signaling pathway. Oncogene 37:3778-3789