Roarke Kamber, PhD

Assistant Professor
Anatomy
Research Description: 

My research interests center on understanding how macrophages detect and eliminate disease-causing cells, including cancer cells, and determining why this homeostatic process fails in aging and disease. To this end, my research encompasses questions in immunology and cancer biology, and leverages a wide range of experimental approaches including genome-wide CRISPR screens, live-cell imaging, biochemical reconstitution, and animal models. We aim to systematically map the inter-cellular signaling axes between macrophages and their target cells that govern phagocytosis, with a particular focus on defining the roles of uncharacterized genes and metabolites in this process. These discovery-based efforts will allow us to understand how macrophages make the all-or-none decision to destroy another cell, to characterize pathological failure modes, and to engineer innate immune cells with enhanced therapeutic properties. The ultimate goal of my research program is to uncover fundamental biological insights that enable next-generation immunotherapies for currently untreatable diseases.

Primary Thematic Area: 
Immunology
Secondary Thematic Area: 
Cancer Biology & Cell Signaling
Research Summary: 
Mechanisms of Macrophage-Mediated Cell Clearance

Websites

Publications: 

Development of compact transcriptional effectors using high-throughput measurements in diverse contexts.

Nature biotechnology

Tycko J, Van MV, DelRosso N, Ye H, Yao D, Valbuena R, Vaughan-Jackson A, Xu X, Ludwig C, Spees K, Liu K, Gu M, Khare V, Mukund AX, Suzuki PH, Arana S, Zhang C, Du PP, Ornstein TS, Hess GT, Kamber RA, Qi LS, Khalil AS, Bintu L, Bassik MC

In vivo perturb-seq of cancer and microenvironment cells dissects oncologic drivers and radiotherapy responses in glioblastoma.

Genome biology

Liu SJ, Zou C, Pak J, Morse A, Pang D, Casey-Clyde T, Borah AA, Wu D, Seo K, O'Loughlin T, Lim DA, Ozawa T, Berger MS, Kamber RA, Weiss WA, Raleigh DR, Gilbert LA

Pathways for macrophage uptake of cell-free circular RNAs.

Molecular cell

Amaya L, Abe B, Liu J, Zhao F, Zhang WL, Chen R, Li R, Wang S, Kamber RA, Tsai MC, Bassik MC, Majeti R, Chang HY

A Genome-Wide CRISPR Screen Identifies Sortilin as the Receptor Responsible for Galectin-1 Lysosomal Trafficking.

bioRxiv : the preprint server for biology

Donnelly J, Kamber RA, Wisnovsky S, Roberts DS, Peltan EL, Bassik MC, Bertozzi CR

Elucidating the cellular determinants of targeted membrane protein degradation by lysosome-targeting chimeras.

Science (New York, N.Y.)

Ahn G, Riley NM, Kamber RA, Wisnovsky S, Moncayo von Hase S, Bassik MC, Banik SM, Bertozzi CR