Interstitial flow, varying from nearly zero in the center of tumor tissue to 4 im/s in the periphery, modulates tumor cell growth and metastasis-i. Tumor cells located in the center of tumor are also subjected to a hypoxic microenvironment, which alters apoptotic, cell cycle and glycosylation pathways. Glycosylation is intimately involved in all steps of metastatic progression by modulating cadherin homophilic interactions (primary tumor) and selectin-ligand (vasculature) as well as integrin-ligand (intravasation, vasculature and extravasation) binding. The overarching goal of Project 3 is to investigate the effects of mechanical forces in prescribed oxygen tension microenvironments on tumor cell signaling and adhesion/migration using a synergistic combination of experimental and compiitational methods.
In Aim 1, we will investigate the effects of interstitial fluid flow and hypoxia on the regulation of intracellular signaling. We will also elucidate the combined effects of hypoxia and low fluid flow on the physics of key receptor-ligand interactions during the multi-step metastatic process (Aim 2). We will next study the effects of steric forces during the intravasation and extravasation process on tumor cell migration (Aim 3) and on intracellular signaling (Aim 4).
In Aim 5, we will investigate tumor cell targeting in vivo using (a) radiolabeled antibodies against CD44 variant isoforms (CD44v) and podocalyxin-like protein (PCLP) and (b) quantum dots conjugated with antibodies specific for CD44v and PCLP that are expressed by metastatic tumor cells but not normal blood cells. Linkage to PS-OC:
The specific aims of Project 3 fit the overarching theme of the Center of the role offerees in the metastatic cascade;
Aims 1 -5 are synergistically connected to Aims 1 and 2 in Project 1 and Aims 1-4 in Project 2 for further research integration of the Center; all Students and Fellows in the Project will be enrolled in the Center Training Program;this project will make use of the resources provided by the Imaging Core and Microfabrication Core, as well as the Administrative Unit of the Center;cell lines and micromechanical methods will be the same as those used in all projects;computational efforts will be shared among all projects.
|Jayatilaka, Hasini; Giri, Anjil; Karl, Michelle et al. (2018) EB1 and cytoplasmic dynein mediate protrusion dynamics for efficient 3-dimensional cell migration. FASEB J 32:1207-1221|
|Jayatilaka, Hasini; Umanzor, Fatima G; Shah, Vishwesh et al. (2018) Tumor cell density regulates matrix metalloproteinases for enhanced migration. Oncotarget 9:32556-32569|
|Lan, Tian; Hung, Shen-Hsiu; Su, Xudong et al. (2018) Integrating transient cellular and nuclear motions to comprehensively describe cell migration patterns. Sci Rep 8:1488|
|Kim, Jeong-Ki; Louhghalam, Arghavan; Lee, Geonhui et al. (2017) Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology. Nat Commun 8:2123|
|Ju, Julia A; Godet, Inês; Ye, I Chae et al. (2017) Hypoxia Selectively Enhances Integrin ?5?1 Receptor Expression in Breast Cancer to Promote Metastasis. Mol Cancer Res 15:723-734|
|He, Lijuan; Sneider, Alexandra; Chen, Weitong et al. (2017) Mammalian Cell Division in 3D Matrices via Quantitative Confocal Reflection Microscopy. J Vis Exp :|
|Semenza, Gregg L (2016) The hypoxic tumor microenvironment: A driving force for breast cancer progression. Biochim Biophys Acta 1863:382-391|
|Zhang, Kun; Grither, Whitney R; Van Hove, Samantha et al. (2016) Mechanical signals regulate and activate SNAIL1 protein to control the fibrogenic response of cancer-associated fibroblasts. J Cell Sci 129:1989-2002|
|He, Lijuan; Chen, Weitong; Wu, Pei-Hsun et al. (2016) Local 3D matrix confinement determines division axis through cell shape. Oncotarget 7:6994-7011|
|Sarnecki, Jacob S; Burns, Kathleen H; Wood, Laura D et al. (2016) A robust nonlinear tissue-component discrimination method for computational pathology. Lab Invest 96:450-8|
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