John DiGiovanni, Ph.D.

John DiGiovanni Profile Pic

Professor of Pharmacology & Toxicology
Coulter R. Sublett Chair
Director CMCT

Research in my laboratory has focused for many years on understanding how cancer develops and on the identification of novel targets, mechanisms and strategies for cancer prevention. Cancer is a disease involving gene-environment interactions and therefore understanding both environmental influences as well as genetic factors is key to developing the most effective strategies for preventing cancer. In addition, understanding the early cellular, biochemical and molecular changes that transform normal cells into cancer cells is essential if we are to eventually eradicate cancer as a major human disease.

There are several major research projects that are currently ongoing in my laboratory.  First, one major research area focuses on identifying specific cellular signaling pathways that are disrupted during tumor development and progression. Signaling pathways currently under study include the PI3K/Akt/mTOR pathway and Signal Transducers and Activators of Transcription (Stats), especially Stats1,3 and 5.  Another important research area involves studies aimed at identifying the target cells (i.e., stem/progenitor cells) for tumor development. Using a novel gene knockout strategy we have recently shown that keratinocyte stem cells located in the bulge region of hair follicles are the major targets for the initiation of skin (epithelial) tumors in mice.  Further study of these cells and their role in tumor development will lead to novel strategies and targets for both prevention and treatment of epithelial cancers. Another important area of research involves identifying genes that confer susceptibility to environmentally-induced cancer. These studies have used genetic crosses between sensitive and resistant mice to map genes involved in the promotion of skin tumors in mice.  Using this approach we recently mapped and identified a gene (Gsta4) on Chr 9 that is involved in susceptibility to skin tumor development in mice.  We also found that polymorphisms in this gene are risk alleles for human non-melanoma skin cancer (both basal cell carcinoma and squamous cell carcinoma).  We are currently examining this gene in other human cancers and also working to identify genes in other regions of mouse chromosomes identified from our initial screen that harbor susceptibility loci.  These studies also incorporate the novel approach of using  “genetical genomics” to help identify novel genes, pathways and networks involved in cancer susceptibility.

A major new research direction in my laboratory focuses on the impact of obesity on cancer development and progression, including obesity that occurs early in life. In fact, obesity in children has risen dramatically in recent years.  Obesity in both adults and children increases risk of cancer development for a number of important cancers. However, the mechanism(s) that underlie the effects of obesity on cancer development and progression are not well understood.  We are currently studying the impact of obesity on cellular signaling pathways in several tissues in relation to its effects on cancer development. Recent studies have revealed that obesity alters growth factor signaling in multiple epithelial tissues through modulation of cross-talk between the IGF-1 and EGF-receptors. The overall goal of this research is to identify molecular targets and strategies to offset the increased cancer risk and mortality associated with obesity.

Cancers currently under study in the laboratory include skin cancer (both melanoma and non-melanoma skin cancers), prostate cancer, head and neck squamous cell carcinoma and lymphoma.

See also:

Biographical Sketch (PDF file)

Recent Publications (PDF file)

Contact Information
Campus location:

US Mail Address:
The University of Texas at Austin
DPRI 2.228
1400 Barbara Jordan Blvd.
Austin, TX 78723

FEDEX Address:
DPRI 2.228
1400 Barbara Jordan Blvd.
Austin, TX 78723