|
Molecular Pathology
of Carcinogenesis
Most of the Molecular Pathology faculty involved
in the study of carcinogenesis are associated with the Department
of Molecular Pathology at M. D. Anderson. The primary focus of
the Department of Molecular Pathology at M. D. Anderson is research
on the genes and gene products involved in the abnormal growth
of tumor cells, and the mechanisms by which these abnormal gene
products induce cancer. The long-term goal of these studies is
to develop new diagnostic reagents and new therapeutic strategies
for cancer. The research activities of the department include several
areas of investigations that relate to these themes.
-
One area concerns gene products of proto-oncogenes
involved in either malignant tumor formation or leukemia. These
particular gene products have been found to possess an important
regulatory enzyme activity (for example, a protein kinase)
that modulates signal transduction in different cellular pathways.
-
A second area of research concerns the
study of a new class of genes involved in prolonging the survival
of non-growing cells by blocking programmed cell death, or
apoptosis. This prolonged survival is believed to enable cells
to undergo further genetic mutations that eventually lead to
a malignant state.
-
A third area concerns the role of cell-adhesion
proteins involved in cell-to-cell interaction, with particular
emphasis on prostate and breast cancers. A recent faculty addition
to the department provides expertise in the study of Proteomics.
Following advances in sequencing the human genome (DNA), the
next challenge is to probe the structure and function of the
proteins encoded by the genome, hence the term "Proteomics."
Other areas of research include:
-
Genes involved in drug resistance
-
Novel and ultrasensitive methods for detecting,
separating and quantitating malignant cells in normal cell
populations in tissue and body fluids
-
Factors required for progression of B-cell
lymphoma
A newly discovered protein kinase that regulates events in mitosis in breast
cancer and other cancers
-
Genes involved in reactive oxygen as they
relate to cancer
-
Genes associated with day/night changes
(the circadian clock) in gene expression as they relate to
cancer and signal transduction pathways involved in cell adhesion
changes in cancer cells
-
HIV vaccines and HIV therapy
-
Retrovirus-mediated gene therapy for treating
cancer
-
Gene therapy for liver disease
Research activities are supported in large part by peer-reviewed grants awarded
to our faculty. These include grants from the National Cancer Institute,
American Cancer Society, and the Department of Defense. Other support is
provided by industrial firms through licensing arrangements on either issued
patents or pending patents. Gift funds provide additional research support
to various investigators in the department.
The department has a core facility laboratory
that provides synthetic peptide reagents and other protein/peptide-related
services for faculty and staff researchers and/or clinicians. Synthetic
peptides are used primarily to produce antibodies as probes for
basic and clinical research. In addition, synthetic peptides are
used as ligands to mimic various ligands, growth factors and cytokines
for protein interaction studies.
Associated Faculty
Ralph
B. Arlinghaus, Ph.D.: Professor
and chairman of the Department of Molecular Pathology at the
University of Texas M. D. Anderson Cancer Center. RNA tumor
viruses (retroviruses), the v-Mos oncoprotein, and the role of
Bcr in Bcr-Abl positive human leukemia.
Jiale Dai, Ph.D: Assistant Professor, Department of
Molecular Pathology at the University of Texas M. D. Anderson Cancer
Center. Molecular genetics and biology of breast cancer.
Madeleine Duvic, M.D.: Professor, Department of Dermatology at
the University of Texas M. D. Anderson Cancer Center. Molecular
Pathogenesis of Skin Diseases
Richard
J. Ford, M.D., Ph.D.: Professor, Chief; Section of Pathobiology,
Department of Molecular Pathology at the University of Texas
M. D. Anderson Cancer Center. Cell growth control in normal
and neoplastic human B lymphocytes.
Peter
R. C. Gascoyne, Ph.D.: Professor,
Department of Molecular Pathology at the University of Texas
M. D. Anderson Cancer Center. Development of dielectric methods
for discriminating between, and isolating, diseased cells and
pathogens.
Peng Huang, M.D., Ph.D.: Associate Professor, Department
of Molecular Pathology at the University of Texas M. D. Anderson
Cancer Center. Biochemical and molecular mechanisms of action
of anticancer agents.
Mien-Chie
Hung, Ph.D.:Chairman, Dept. of Molecular and Cellular Oncology,
Director, Breast Cancer Basic Research Program, Ruth Legett Jones
Distinguished Chair Professor. Oncogenes, Tumor Suppressor
Genes, Signal Transduction, and Gene Therapy.
Ryuji Kobayashi,
Ph.D.: Professor, Department
of Molecular Pathology at the University of Texas M. D. Anderson
Cancer Center. Method development in proteomics research;
Bcr-Abl signaling in leukemia; TCL-1 function in T-cell tumorigenesis;
protein S-nitrosylation.
M. Tien Kuo,
Ph.D.: Felix
L. Haas Professor in Basic Science Department of Molecular Pathology
Chief, Section of Eukaryotic Cell Research, Department of Molecular Pathology
at the University of Texas M. D. Anderson Cancer. Evolution of drug resistance
and tumor development; Targeted prodrug therapy of liver cancers; Genomic instability
and evolution of drug resistance.
Sue-Hwa Lin, Ph.D.: Professor, Department
of Molecular Pathology at the University of Texas M. D. Anderson
Cancer Center. Prostate cancer bone metastasis; Roles of
CEACAM1 cell adhesion molecule in prostate cancer; Roles of
anti-angiogenic protein 16-kDa prolactin in prostate cancer.
Timothy
J. McDonnell, M.D., Ph.D.: Professor, Department
of Molecular Pathology at the University of Texas M. D. Anderson
Cancer Center. Molecular oncology; Molecular determinants
of therapeutic response
Jagannadha K. Sastry, Ph.D.:Professor,
Department of Immunology at
the University of Texas M. D. Anderson Cancer Center. HIV-AIDS;
cervical cancer; vaccines; cellular immunology; synthetic peptides.
Elizabeth
L. Travis, Ph.D.: Professor, Experimental and Radiation Oncology at
the University of Texas M. D. Anderson Cancer Center. Radiation-induced
fibrosis; genetic basis of tissue radiation sensitivity and fibrosis;
growth factors. |