Steven B. McMahon, PhD
233 S. Tenth Street, Suite 609
Philadelphia, PA 19107
Most Recent Peer-reviewed Publications
- Retraction Notice to: Nuclear receptor function requires a TFTC-type histone acetyl transferase complex
- USP22 regulates oncogenic signaling pathways to drive lethal cancer progression
- The epigenetic modifier ubiquitin-specific protease 22 (USP22) regulates embryonic stem cell differentiation via transcriptional repression of sex-determining region Y-box 2 (SOX2)
- P53: The TRiC Is Knowing When to Fold 'Em
- Acetylation of the cell-fate factor dachshund determines p53 binding and signaling modules in breast cancer
PhD, Immunology, University of Pennsylvania
MS, Physiology, Temple University
BS, Biology, Albright College
Expertise & Research Interests
Our group has a long-standing interest in understanding the biochemical events that are deregulated to cause alterations in broad transcriptional programs in human cancer. As such, our research focuses on the two most commonly mutated transcription factors, MYC and p53, that are critical to cancer progression. We are currently focused on defining precisely how MYC and p53 are regulated in cancer cells, how the transcription programs they control are altered in cancer, and ultimately what essential cellular processes are impacted by these changes. Collectively, these studies have identified previously unknown nodes in these pathways that may represent potential therapeutic targets.
Current Research Projects
- Understand the role of altered mitochondrial transcription in the ability of MYC to reprogram cellular metabolism during malignant transformation.
- Identify the mechanism by which post-translational modifications control the ability of the p53 tumor suppressor to selectively activate distinct transcriptomes.
- Define the contribution of genetic lesions in subunits of the human SAGA coactivator complex to human cancer.