Dr. Minna Roh-Johnson
Little things. big impact.

Dr. Minna Roh-Johnson

At the crossroads of motion and medicine

Assistant Professor of Biochemistry  |  University of Utah

Decoding cancer cell migration.

Dr. Minna Roh-Johnson leads the University of Utah’s biochemistry lab. The primary focus of her research is cell biology and unlocking the mysteries of cell migration, particularly in cancer cells.

Breakthroughs by Dr. Roh-Johnson

Focal adhesion in vivo

Zebrafish earn their stripes.

Understanding how melanoma cells migrate requires in vivo study. Central to the issue is focal adhesion, or how cancer cells attach to an underlying substrate. Despite years of research, the organization of these structures is still unclear.


Dr. Roh-Johnson’s lab has developed an innovative system in zebrafish larvae that allows them to observe the formation of focal adhesion structures in highly migratory melanoma cells on the surface of the skin.

They have used this system to dissect the composition and dynamics of focal adhesion structures and have identified unique properties of cancer cells in their native environments. This deeper understanding of focal adhesion formation is a positive step toward therapies to prevent it.


From Dr. Roh-Johnson's lab

  • Cancer cells interacting with matrix in vivo.

    Cancer cells on the move

    Cancer cells interacting with matrix in vivo. Zebrafish melanoma cells (magenta) physically interact with collagen fibrils (green) during cell migration in vivo.

  • Cancer cells form focal adhesion structures at the base of actin-rich protrusions.

    Focal adhesions in action

    Cancer cells form focal adhesion structures at the base of actin-rich protrusions. Zebrafish melanoma cells expressing Paxillin (green) and Lifeact to visualize actin (magenta).

  • Cancer cells form actin-rich structures during cell migration in vivo

    Tracking melanoma in zebrafish

    Cancer cells form actin-rich structures during cell migration in vivo. Zebrafish melanoma cells expressing Lifeact-EGFP transplanted into a four-day post-fertilization zebrafish larva.

The best results are when you see something you didn't expect under the microscope.

Dr. Minna Roh-Johnson University of Utah

Breakthroughs by Dr. Roh-Johnson

The power of CAR-Ms

Micromanaging macrophages.

The recent development of chimeric antigen receptor macrophages (CAR-M’s) to create a proper anti-tumor macrophage phenotype hasopened new possibilities for therapeutic cancer interventions.

The premise is that macrophages can readily infiltrate solid tumors. If a macrophage can be taught to engulf a specific cancer cell, and is then introduced to the cancer environment, it could be the basis for a powerful therapeutic.

Breakthroughs by Dr. Roh-Johnson

Macrophages in metastasis

Decoding macrophage messages.

The recent development of chimeric antigen receptor macrophages (CAR-M’s) to create a proper anti-tumor macrophage phenotype hasopened new possibilities for therapeutic cancer interventions.

The premise is that macrophages can readily infiltrate solid tumors. If a macrophage can be taught to engulf a specific cancer cell, and is then introduced to the cancer environment, it could be the basis for a powerful therapeutic.

From Dr. Roh-Johnson's lab

  • MDA MDA 231 breast cancer cells with RFP-tagged mitochondria labelled with MitoTracker Deep Red (magenta) and LysoTracker (cyan).

    Mitochondrial heterogeneity in breast cancer cells

    MDA MDA 231 breast cancer cells with RFP-tagged mitochondria labelled with MitoTracker Deep Red (magenta) and LysoTracker (cyan).

  • Mitochondrial fragmentation

    Mitochondrial fragmentation

    Primary human macrophages expressing mitochondrially-localized mEmerald differentiated into an M2-like anti-tumor macrophage state exhibits increased mitochondrial fragmentation.

  • Primary human macrophages (green) transfer mitochondria to MDA MB 231 breast cancer cells (red)

    Tracking melanoma in zebrafish

    Primary human macrophages (green) transfer mitochondria to MDA MB 231 breast cancer cells (red). Arrowheads mark transferred macrophage mitochondria in breast cancer cells.

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