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UNIVERSITY OF SOUTH CAROLINA
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Arnold School of Public Health
University of South Carolina
800 Sumter Street
Columbia, SC 29208

Phone: 803-777-5032
Fax: 803-777-4783

 

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Tara    Sabo-Attwood  Ph.D.
Assistant Professor

Public Health Research Center (PHRC), 401C
921 Assembly Street
Columbia, SC 29208

Secondary Address:
None

Sabo-Attwood Laboratory Website

Phone: (803) 777-4120
Fax: (803) 777-3391
Email: saboattw@mailbox.sc.edu

Biographical Information:
2003-2005, Postdoctoral Fellow, Department of Environmental Pathology, University of Vermont
2003, Ph.D., Environmental Toxicology, University of Florida
1996, B.S., Cytogenetics, University of Connecticut


Honors & Awards:
2004, Postdoctoral Vermont Cancer Center Award, University of Vermont
2003, Patent for Largemouth bass gene chip, University of Florida (EcoArray Inc.)
2003, NIEHS Postdoctoral Fellowship, University of Vermont
2003, Graduate Student Competition Award-Pollutant Responses in Marine Organisms (PRIMO)
2001, Medical Guild Departmental Competition, University of Florida, Gainesville FL


Research:
Research Interests:

• Cell signaling pathways impacted by airborne pollutants (asbestos, smoke, nanoparticles) relevant to environmental lung disease

• The role of estrogen in lung cancer

• Molecular mechanisms of xenoestrogens in aquatic models (zebrafish)

Airborne pollutants and environmental lung disease

Occupational and environmental exposure to airborne pollutants is associated with the development of chronic lung disease including cancer, fibrosis, bronchitis, and asthma, among others. The molecular pathways perturbed by these pollutants (asbestos, smoke, nanoparticles) is not clear, and elucidation of these signaling cascades and control of critical downstream gene targets in lung cells is the focus of my research.

Using a toxicogenomic approach, we have discovered several candidate genes (MUCs and Clca1) that may be important in particulate-induced lung disease and are specifically involved in the production and regulation of mucin secretion in the lung. Airway mucus hypersecretion is a prominent feature of chronic lung pathologies, and elucidation of signaling pathways stimulated by airborne pollutants that regulate mucus metaplasia will lead to both a better understanding of basic biology of chronic pulmonary diseases as well as potential therapeutic targets. We are currently investigating the role of EGFR/MAPK signaling pathways in the transcriptional regulation of these genes through in vitro and in vivo applications including microarrays, siRNA, chemical inhibition studies, immunohistochemistry, and transgenic animals.

In a related focus, we are also investigating the role of estrogen receptors in lung disease. The increasing incidence of female non-smokers with lung cancer (adenocarcinoma) has led to speculation that estrogen plays a role in disease development and/or progression. Estrogen receptors have been recently discovered in the lung and are overexpressed in some tumors, but the role they play in regulation of cell growth, death, metastasis, and therapeutic resistance is currently unknown.

Endocrine disruption in aquatic model systems

Many estrogen active compounds (xenoestrogens), including components of pesticides, herbicides, insecticides, industrial chemicals, and pharmaceuticals have been causally associated with adverse effects on wildlife and human populations, contributing to impaired reproductive success, developmental abnormalities, and cancer incidence. Xenoestrogens bind and activate estrogen receptors, which are transcription factors that regulate downstream gene targets involved in growth, reproduction, and development. Estrogen signaling pathways have become increasingly complex with the discovery of additional receptor subtypes,  and . Investigating the functional roles of the receptor isotypes in aquatic models (zebrafish) in response to estrogen and environmental contaminants is currently underway using molecular techniques including microarrays and morpholino knockdown.


Selected Publications:

Norman, R.S., J.W. Stone, A. Gole, C.J. Murphy, and T.L. Sabo-Attwood. (2007). Targeted photothermal lysis of the pathogenic bacteria, Pseudomonas aeruginosa using gold nanorods. Nano Letters (In Review).

Christopher B. Manning, Tara Sabo-Attwood, Raymond F. Robledo, Maximilian B. MacPherson, Mercedes Rincon, Pamela Vacek, David Hemenway, Douglas J Taatjes, Patty J. Lee, and Brooke T. Mossman. (2007) Targeting the MEK1 Cascade Alters Proliferation and Differentiation of Bronchiolar Epithelium after Asbestos Inhalation. (In Review).

Fukagawa N, Muyao L, Sabo-Attwood T, Timblin C, Butnor K, Gagne J, Steele C, Taatjes D, Huber S, and Mossman BT. (2007) Airborne Pathogenic Particulates Exacerbate Atherosclerosis in ApoE Deficient Mice via CD4+ T Cells. (In Review)

Tara Sabo-Attwood, Jason L Blum, Kevin J Kroll, Vishal Patel, Detlef Birkholz, Nancy J Szabo, Suzanne Z Fisher, Robert McKenna, Martha Campbell-Thompson and Nancy D Denslow. (2007) Distinct expression and activity profiles of largemouth bass estrogen receptors in response to estradiol and nonylphenol. J Mol Endo (In Press).

Maria E Ramos-Nino, Steve R Blumen, Tara Sabo-Attwood, Joanna Gell, Harvey Pass, Maurizio Bocchetta, Deborah Altomare, Barbara Kroczynska, Michele Carbone, Joseph Testa, Nicholas Heintz, and Brooke T. (2007) Mossman. Complex Regulation of Fra-1 in Human Mesotheliomas. Am J Respir Cell Mol Biol. Sep 13.

Raj JU, Aliferis C, Caprioli RM, Cowley Jr AW, Davies PF, Duncan MW, Erle DJ, Erzurum SC, Finn PW, Ischiropoulos H, Kaminski N, Kleeberger SR, Leikauf GD, Loyd JE, Martin TR, Matalon S, Moore JH, Quackenbush J, Sabo-Attwood T, Shapiro SD, Schnitzer JE, Schwartz DA, Schwiebert LM, Sheppard D, Ware LB, Weiss ST, Whitsett JA, Wurfel MM, Matthay MA. (2007) Genomics and Proteomics of Lung Disease. Am J Physiol Lung Cell Mol Physiol. Apr 27.

Sabo-Attwood, T. , Ramos, M.E., Bond, J., Butnor, K., Heintz, N., Gruber, A., Vacek, P., and Mossman, B.T. (2005) Gene Expression Profiles Reveal Increased mCLCA3 Expression and Mucus Metaplasia in a Murine Model of Asbestos-Induced Fibrogenesis. Am J Pathol. 2005 Nov;167(5):1243-56.

Ramos-Nino, ME, Vianale, G., Sabo-Atwood, T. , Mutti, L., and Mossman, B.T. (2004) Human Mesothelioma Cells Exhibit Tumor Cell-Specific Differences in Phosphatidylinositol 3-kinase/AKT Activity that Predict the Efficacy of Onconase. Molecular Cancer Therapeutics 2005; 4(5).

Sabo-Attwood, T. , Ramos, M.E., Bond, J., Butnor, K., Heintz, N., Gruber, A., Vacek, P., and Mossman, B.T. (2005) Gene Expression Profiles Reveal Increased mCLCA3 Expression and Mucus Metaplasia in a Murine Model of Asbestos-Induced Fibrogenesis. Am J Pathol. 2005 Nov;167(5):1243-56.

Sabo-Attwood, T. , Kroll, KJ, and Denslow, N.D. (2004) Differential Expression of Largemouth Bass Estrogen Receptor Isotypes Alpha, Beta, and Gamma By Estradiol. Molecular and Cellular Endocrinology 218, 107-118.

Larkin, P., Sabo-Attwood, T. , Kelso, J., and Denslow, ND. (2003) Analysis of gene expression profiles in largemouth bass exposed to the endogenous hormone, estradiol, and the environmental contaminants, nonylphenol, and p, p'-DDE. EcoToxicology 12, 463-468.

Sabo-Attwood, T. , Larkin, P., Kelso, J., and Denslow, N.D. (2002) Gene expression profiles of largemouth bass exposed to nonylphenol and ICI 182,780. Endocrine Disruptors: Mechanisms and Impacts, International Congress on the Biology of Fish, 17-28.

Larkin, P., Sabo-Attwood, T. , Kelso, J., and Denslow, N. (2002) Gene expression analysis of largemouth bass to estradiol, nonylphenol, and p,p'-DDE. Comparative Biochemistry and Physiology Special Issue, Functional Genomics, 133, 543-557.


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