DREAM complex · Quiescence · Tumor suppression

How cells stop dividing—and how cancers escape the brake

The Litovchick laboratory investigates the molecular systems that decide whether a cell proliferates, enters quiescence or resumes growth. By studying the DREAM complex, DYRK1A signalling and RB-family tumor suppressors, the group aims to explain how cell-cycle control is lost in cancer and how that loss can be exploited therapeutically.

Litovchick Lab research

Our research

One molecular switch. Many cell-fate consequences.

The Litovchick laboratory studies how cells enter, maintain and escape quiescence, with a particular focus on the DREAM transcriptional repressor complex and its control of cell-cycle gene expression. The group connects the molecular assembly of DREAM—through RB-family proteins, E2F factors, the MuvB core and the DYRK1A kinase—to tumor suppression, cancer-cell dormancy and treatment response. Current work extends these mechanisms into lung cancer, ovarian cancer, HPV-associated disease and mutant-p53 non-small-cell lung cancer, seeking vulnerabilities that can convert growth arrest from a protective state into a therapeutic opportunity.

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Larisa Litovchick, M.D., Ph.D.

Principal investigator

Larisa Litovchick, M.D., Ph.D.

Associate Professor of Internal Medicine

Larisa Litovchick, M.D., Ph.D., is an Associate Professor in the Department of Internal Medicine at Virginia Commonwealth University School of Medicine and a member of the Cancer Biology research program at VCU Massey Comprehensive Cancer Center. She is an Associate Director in VCU's physician-scientist training environment and has a long-standing record of NIH- and DOD-supported research on the evolutionarily conserved DREAM transcriptional repressor complex. Her work helped define mammalian DREAM, identify the DYRK1A–LIN52 phosphorylation mechanism required for its assembly, and establish links between DREAM activity, cellular quiescence, tumor dormancy and cancer therapy response.

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