|
Faculty |
Cancers Studied |
Description of Research |
|
Sherif Abdel-Rahman |
General |
In my laboratory, the focus is on
toxicogenomic and pharmacogenomic research. I am specifically interested in understanding how
inherited genetic characteristics influence the susceptibility of individuals to environmental
agents and affect their response to drug therapy. |
|
Xiaodong Cheng |
Ovarian
Pancreatic |
The major research focus in our laboratory is
function and regulation of protein kinases and small GTPases and their roles in cancers. We are
also conducting study of the molecular mechanism of ovarian cell transformation and
tumorgenesis using a genetically defined ovarian cancer model and functional proteomics
approaches. |
|
Dai Chung |
Neuroblastoma |
Our ongoing projects include (1) characterizing
expression of GRP and GRP-R in various clinical stages of neuroblastomas, (2) determining
mechanisms involved in the regulation of GRP-R gene and protein expression, and (3) identifying
the role of phosphatidylinositol 3-kinase in GRP-induced proliferation of neuroblastomas. |
|
Tom Albrecht |
Viral-induced |
Our research program investigates the
relationship of human cytomegalovirus (HCMV) to oncogenic processes. Our work has shown that
HCMV interacts with chemical carcinogens or radiation to induce more-than-additive, usually
synergistic, increases in genetic damage endpoints. We are now investigating the mechanisms
through which these effects may occur, including cellular signal transduction, perturbation of
cell cycle regulation, and interference with repair processes and programmed cell death. |
|
Cornelis Elferink |
Liver |
Toxins, pathogenic infection (viral and
bacterial), and physical injury to the liver results in a loss of hepatic tissue, triggering a
regenerative response intent on restoring liver cell mass. Dysregulation in the repair process
can lead to liver failure or liver cancer. The aryl hydrocarbon receptor (AhR) is a
ligand-activated transcription factor functionally identified with proliferative and apoptotic
processes. Exposure to the prototypical AhR ligand (TCDD, dioxin) induces a host of toxic and
adaptive endpoints, including inhibition of liver regeneration following tissue injury. Our
long-term goal is to understand mechanistically how the AhR contributes to liver homeostasis by
regulating cell proliferation and apoptosis, and thereby identify the molecular basis for
TCDD-induced disruption of normal biological processes. |
|
Lisa Elferink |
Liver
Pancreatic |
We are interested in how dysregulated cMet
endocytosis and down regulation contribute to the dissemination and metastases of pancreatic
and hepatocellular carcinomas. The intensity, duration and specificity of signal transduction
through cMet are regulated by ligand-mediated endocytosis and lysosomal degradation. Sustained
signaling from the receptor tyrosine kinase cMet correlates with early stage invasion,
dissemination and metastases of several aggressive human gastrointestinal cancers particularly
pancreatic adenocarcinomas and hepatocellular carcinomas. |
|
Rinat Esenaliev |
Breast
Colon
Ovarian
Prostate |
My cancer-related research includes drug
and gene delivery in tumor cells with novel techniques. We study enhancement of anti-cancer
drug and gene delivery in vitro and in vivo in nude mice bearing human colon, breast, prostate,
or ovarian tumors.
|
|
Mark Evers |
GI cancers |
Current research interests include the
evaluation of cellular mechanisms leading to the differentiation of the developing intestine
and the growth of normal and neoplastic GI tissues. Another area of active interest in the
laboratory is the better understanding of the signaling pathways which contribute to intestinal
cell differentiation. |
|
Miriam Falzon |
Breast
Colon |
PTHrP is able to enter the nucleus and/or
nucleolus and influence cell cycle progression and apoptosis (intracrine effects). We are
studying the effects of PTHrP on cell proliferation of breast cancer cells. We have shown that
PTHrP localizes to the nucleus and produces a net increase in breast cancer cell proliferation.
The mechanism for this effect is being investigated with respect to cell cycle regulation.
|
|
David Gorenstein |
Drug design |
We have a major program oriented toward the
combinatorial selection, rational design, synthesis and structural characterization of
oligonucleotide analogues (especially dithiophosphate analogues selected from large
combinatorial libraries - "thioaptamers") and other agents directed toward manipulation of key
proteins involved in inflammation and cancer such as NF-KappaB. In addition multidimensional
NMR is currently being carried out on the thioaptamer agents and protein complexes and these
are used for development of a proteomics chip. |
|
Tianyan Gao |
General |
The focus of my lab is to
study molecular mechanisms underlying the regulation of a novel protein phosphatase
named PHLPP. Research involves identification of novel interacting proteins,
biochemical characterization of signal transduction pathways governing the phosphatase
activity, and investigation of the tumor suppressor function of the phosphatase in mouse
models. |
|
Owen Hamill |
General |
We are interested in the role of
mechanosensitive channels and Ca2+ signaling in tumor cell migration and invasion. We
study prostate tumor cells and use patch clamp recording, Ca2+ imaging and molecular biological
techniques. Our aim is to understand the signaling pathways that switch a cell from a
nonmigratory to a migratory phenotype. |
|
Mark
Hellmich |
Colon
GI
Ovarian
|
My major research interest is in the elucidation of signaling
pathways regulated by heptahelical
G-protein linked peptide hormone receptors of gastrointestinal tracts, specifically those
pathways coupled to the bombesin and gastrin family of receptors. |
|
Jianhang Jia |
General |
The objective of the research in Dr. Jia's laboratory is to
elucidate the mechanisms by which Hedgehog signal is transduced. Studies on the components of
the Hh signaling pathway may provide new avenues for developing diagnostic tools and
therapeutic treatment of cancers which associate with dysregulation of Hh signaling.
|
|
Stanley M. Lemon |
Liver
Viral-induced |
My laboratory works on the
pathogenesis of hepatitis C virus infections, and the role of this virus in the development of
primary hepatocellular carcinoma. |
|
Chunming Liu |
Colon |
Dr. Liu's Lab studies the molecular mechanism of
Wnt/beta-catenin signaling and JAK/STAT signaling, and the role of these signaling pathways in
development, oncogenesis and stem cell self-renewal. |
|
Bruce
A. Luxon |
General
Bioinformatics
Drug discovery |
Research in my lab covers a broad range of
interests including bioinformatics, genomics, proteomics, metabolomics, and systems biology. We
also have programs for the development of novel thioaptamer-based diagnostics and therapeutics
targeting infectious disease and cancer. We are especially interested in the EGFR and
other RTKs as targets for cancer therapeutics. |
|
Lee-Jane Lu |
Breast Cancer |
Our lab studies breast cancer prevention,
public health; breast cancer biomarker discovery; diet and breast cancer |
|
Luis
Martinez |
Breast |
My lab is interested in determining the underlying mechanism(s) for mtp53’s oncogenic activity.
The long-term aim of the lab is to elucidate the critical functions mutant p53 utilizes to
promote cancer development, in order to generate new targets for therapeutic intervention. |
|
Sankar Mitra |
General |
Linkage of cancer induction and treatment
to DNA damage repair |
|
Kathleen
O'Connor |
Breast
Pancreatic
Colon
|
Our lab is interested in understanding how
advanced cancers, specifically carcinomas, invade and metastasize. Specific areas of active
investigation are centered around understand how integrins and integrin signaling control cAMP
metabolism, Rho family GTPases and gene transcription and thereby contribute to the aggressive
behavior of advanced cancers. |
|
Don Powell |
Colon |
The Powell laboratory studies the colon
cancer microenvironment; i.e., epithelial/mesenchymal interactions between the colonic stroma
and normal, adenoma and carcinoma colonic epithelia. We are
particularly interested in the biology and role of “activated” fibroblast (myofibroblasts)
which constitutively express COX-2 and other factors that contribute to colon tumor
progression. |
|
Louise Prakash |
General |
Translesion synthesis across
mutagenic/carcinogenic DNA lesions |
|
Satya Prakash |
General |
Translesion synthesis across
mutagenic/carcinogenic DNA lesions |
|
Vicente Resto |
General with emphasis on head and neck cancers |
My laboratory focuses
on the study of lymphatic metastasis with special interest in the molecular mediators of
lodgment and growth of tumor cells within the lymph node microenvironment. Furthermore,
we are interested in understanding the impact these interactions have towards promoting tumor
tolerance by the immune system. To these ends, we apply functional genetic screening,
biophysical, and biochemical techniques to the study of this novel biology. |
|
Sarita
Sastry |
Colon |
My lab studies the role of protein tyrosine phosphatase in
controlling cell migration. My long-term goal is to understand their function and regulation
during tumor cell invasion and tumor angiogenesis. |
|
Pomila Singh |
GI Cancers |
.Dr.
Singh's laboratory is conducting research in the area of hormones and growth factors as it
relates to colon carcinogenesis.
|
|
E.
Brad Thompson |
General |
1. Steroid hormones and cancers of several
types.
2. Use of peptide therapy for groove and hematologous malignancies. |
|
Shahid Umar |
Colon |
To understand: how pro-inflammatory
cytokines and dietary fiber regulate nuclear factor-kB (NF-kB) and -catenin mediated increases
in cell census in the colon in the absence and presence of chronic inflammation and, whether
these conditions facilitate subsequent mucosal priming for colon carcinogenesis. |
|
Roger A.
Vertrees |
Lung cancer |
My lab is a translational lab that deals
with all aspects of the pathobiology of lung cancer from cell culture and study of mechanisms
to clinical trials. Our long range goal is to developing new therapies for patients with lung
cancer. Working with Dr. Zwischenberger we have developed an extracorporeal method of
delivering hyperthermia to patients with this disease and in our first clinical trial
demonstrated significant beneficial effects of hyperthermia. |
|
Jon Ward |
Hematopoietic
Carcinogenesis |
Dr. Ward's research focuses on the effects
of exposures to genotoxic chemicals in the environment. A particular focus of his research is
on understanding the mechanisms by which 1,3-butadiene, a carcinogenic chemical used in rubber
manufacturing and a common air pollutant, induces mutations in occupationally exposed human
subjects and in mice. |
|
Cheryl S. Watson |
Breast Pituitary
Lymphoid
Tumors |
Dr. Watson's work centers on the basic
mechanisms of steroid hormone action, specializing more recently in nongenomic pathways. Her
publications focus on cellular mechanisms of signaling involved in the growth of breast,
pituitary, and lymphoid tumors. She also studies the signaling pathways by which estrogen
mimetics (environmental estrogens, phytoestrogens) act on these tumor and organ systems. |
|
Jingwu Xie |
Gastric
Medulablastoma
Basal Cell
Pancreatic |
The main focus in Dr. Xie's laboratory is to investigate genetic
alterations of cancer, particularly the hedgehog signaling transduction pathway, and its role
in the development of cancer. |
|
Peter
(Binhua) Zhou |
Breast |
Metastasis, the spread of cells from a primary tumor to distant
sites, is the main cause of death in patients with cancer. Our long-term goal is to eliminate
the incidence of cancer metastasis by understanding the molecular mechanism underlying the
initial step of metastasis. |