Kevin Roarty Lab

Research Areas

Building and maintaining the mammary gland

The mammary gland is one of the few organs that develops largely after birth and remodels repeatedly across a lifetime. We investigate how canonical and alternative (β-catenin-independent) Wnt signals, including those routed through Ror-family receptors, are integrated within epithelial subsets to direct branching, position cells correctly within the tissue, and sustain the gland at steady state. A central question is how a single pathway achieves such specific outcomes depending on which cell receives the signal and when.

Cell identity, fate, and plasticity

Cells in the breast are not locked into fixed roles. We examine how epithelial cells acquire, maintain, and lose their identities, and how the plasticity that serves normal tissue becomes a liability once it is redeployed in cancer. This work addresses how heterogeneity within a tumor arises, how transitional and hybrid cell states are stabilized, and what those states contribute to progression.

Tumor ecosystems, adaptation, and metastatic vulnerability

Metastasis is rarely the work of one cell type acting alone. We treat the tumor as an ecosystem, in which subpopulations of cancer cells coordinate with one another and with stromal, immune, and vascular neighbors within a supporting matrix. What makes this ecosystem formidable is its adaptability. As cells leave the primary site and encounter the very different niche of a distant organ, the collective reorganizes itself: roles are reassigned, dependencies shift, and the group reconstitutes a functioning community in foreign tissue. Following that process from the breast outward, with an emphasis on the lung, we ask which coordinated behaviors and which niche interactions the ecosystem cannot do without. Those dependencies are the vulnerabilities we aim to target.

Approaches and Technologies

Our model systems include three-dimensional organoid culture, genetically engineered and syngeneic mouse models, patient-derived xenografts, and primary patient specimens. We visualize these systems by confocal and second harmonic generation microscopy, along with live imaging of tissue dynamics. To resolve the cell states and interactions underlying what we observe, we apply single-cell and spatial transcriptomics, flow cytometry, and additional multi-omics approaches.

The Lab

Our team is listed on the Lab Members page.