ResearchLarge8

 

Mechanisms of Carcinoma Progression: From Bench to Bedside

Arthur M. Mercurio

We are interested in the mechanisms that underlie the genesis of high-grade, aggressive carcinomas of the breast and prostate. Our reserach is rooted in the hypothesis that high-grade carcinomas are characterized by specific autocrine signaling pathways involving growth factor (VEGF) receptors and integrins, and that autocrine signaling promotes a de-differentiated, EMT phenotype and increases the frequecy and self-renewal of tumor-initiating/stem cells.  Components of this autocrine singaling pathway are prime targets for therapeutic intervention.


ResearchLarge8

 

Cell Death and Autophagy

Eric Baehrecke

Our laboratory studies the mechanisms that regulate autophagy, cell survival and programmed cell death in the context of normal and abnormal development. Altered autophagy, cell survival and cell death are associated with a variety of human disorders including cancer.


ResearchLarge8

 

Genetic Control of Programmed Cell Death (Apoptosis) in Drosophila

Andreas Bergmann

The long-term objective of our research is to gain a comprehensive understanding of the genetic control of apoptosis and cell proliferation, and their connection to human cancer. Apoptosis and cell proliferation are critical for normal development, homeostasis and aging.


ResearchLarge8

 

Hereditary Breast Cancer

Sharon Cantor

Breast cancer is the most common hereditary cancer syndrome in the United States. Two genes are associated with hereditary cancer, BRCA1 and BRCA2. Mutations in these genes predispose women to early onset breast and ovarian cancer


ResearchLarge8

 

Cancer Epidemiology; Prenatal Origin of Cancer

Chung-Cheng Hsieh

Our laboratory area of interest is cancer epidemiology with research focusing on (1) prenatal origin of cancer risk, with special interest in the association of stem cells and perinatal factors with breast cancer risk, (2) gestational characteristics and maternal risk for breast and ovarian cancer, and (3) breast cancer risk factors for women of different ethnic backgrounds.


ResearchLarge8

 

Mouse models of leukemia

Michelle A. Kelliher

Aberrant expression of developmentally important regulatory genes has been increasingly implicated among hematopoietic malignancies. Abnormalities in either abundance or activity of these gene products can result in inappropriate expression of genes critical to the processes of cell growth and differentiation.


ResearchLarge8

 

Adult Epithelial Stem Cells

Stephen Lyle

We are interested in key molecular and cell biologic properties of cancer stem cells, which are responsible for tumor growth, recurrence and metastasis.  We are applying techniques and knowledge developed in earlier studies of normal epithelial stem cells to characterize cellular subsets of human tumors that display stem cell properties.  The ultimate goal is to more efficiently target chemoresistant cancer stem cells for destruction, leading to better patient outcomes. 


ResearchLarge3

 

The Hedgehog (Hh) Signaling Pathway in Development and Cancer

Junhao Mao

My lab is interested in the molecular mechanisms that underlie organogenesis and tumorigenesis of the gastrointestinal tract.  Our work is focused on the regulation of several key signaling pathways such as The Hedgehog (Hh), Wnt and BMP.  We use a combination of transgenic mouse models and cellular approaches to identify their roles in stem cell/progenitor function, epithelial-mesenchymal interactions, and their contribution to gastrointestinal tumor intiation and progression.


ResearchLarge10

 

Insulin Receptor Substrate Signaling in Breast Cancer

Leslie Shaw

The research interests of the Shaw Lab are aimed at understanding the mechanisms involved in the progression of cancer from carcinoma in situ to metastatic disease. Progression requires that these cells acquire the abilities to invade, survive in non-breast tissues and stimulate angiogenesis. One of the major interests of the lab is the contribution of Insulin Receptor Substrate (IRS)-dependent signaling pathways to breast cancer progression. The IRS proteins are adaptor proteins that are recruited to surface receptors in response to ligand binding where they organize complexes that initiate intracellular signaling cascades.


ResearchLarge8

 

Epithelial Mesenchymal Transition and Cancer Progression

Karl Simin

Our current research is focused on the role of tight junction complexes in regulating epithelial to mesenchymal transition (EMT) and invasive cell behavior. EMT describes processes that cause epithelial cells, which normally form sheets of interconnected cells, to dissemble their intercellular junctions, lose apical-basal polarity, and acquire mesenchymal characteristics, such as increased motility.


ResearchLarge11

 

The interactions between epigenomics, cell differentiation and the cell cycle

Merav Socolovsky

We study the interactions between epigenomics, cell division and differentiation in the erythropoietic system. We recently found that erythropoiesis entails genome-wide loss of DNA methylation, a process that was previously thought to be limited to pluripotent cells in the early embryo. We also found that erythroiod gene transcription is activated by a cell fate switch that is closely orchestrated by DNA replication. Dysregulation of the molecular pathways that underlie these effects is likely to contribute to blood cancers.