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Call for Award Nominations

Please strongly encourage your graduate students and postdocs to submit abstracts and apply for the PostDoc and Graduate Student Best Abstract Awards for EB2010. The links for the Award applications are below. Be sure to select the Toxicology Division.

Graduate Student Best Abstract Award (GSBPA):

http://www.aspet.org/awards/grad_student_abstract/

Postdoctoral Scientist Award (PostDocSci):

http://www.aspet.org/awards/postdoctoral_scientist/

The prize for the single Postdoctoral Scientist award is $500, while prizes for the 1st, 2nd, and 3rd Graduate Student Best Paper Awards are $500, $300, and $200, respectively. A Graduate Student-Postdoc Best Abstract Competition and Student-Mentor Mixer will be held, during which the posters will be judged, and winners identified. The winners will also be announced at the Division for Toxicology Business Meeting. Winning posters will also be displayed at the joint mixer in combination with the Division for Drug Metabolism. This provides a large and interested audience for your students and postdocs, and is a great opportunity for them to network.

In addition, ASPET provides a number of Travel Awards to EB2010, including Graduate Student Travel Awards, Minority Graduate Student Travel Awards, Young Scientist Travel Awards, Minority Young Scientist Travel Awards, and Summer Undergraduate Research Fellow Travel Awards. Information for the Travel Awards can be found at ASPET website: http://www.aspet.org/awards/travel/.
 

Call for Symposium Proposals

The Division for Toxicology of ASPET is soliciting proposals for Division-sponsored symposia for the Experimental Biology 2011 meeting. While it seems early, we need your input now regarding topics that you would like to develop and organize, or suggestions of cutting-edge science for the officers of the Division for Toxicology to consider and pursue.  The Program Committee of ASPET will meet later this fall to begin planning and developing symposia, with final decisions made in February.  Please consider organizing a symposium; this is an excellent opportunity to bring the leaders of your field together for a timely session that could attract a potentially large audience of Experimental Biology attendees. The Division for Toxicology frequently co-sponsors symposia with other Divisions (e.g., Drug Metabolism, Neuropharmacology, or Cardiovascular Pharmacology), so feel free to think broadly.  Financial assistance is available from ASPET to help cover the speaker registration and travel expenses. Clear and simple guidelines and an on-line submission form are available on the ASPET web site (again, please select Toxicology as the appropriate Division)

 

Please submit your preliminary ideas and plans to Dr. Qiang Ma (Division Chair) at qam1@cdc.gov no later than November 14 so that we can have a list of topics ready for the fall meeting of the ASPET Program Committee.

 

Membership in the Division for Toxicology

and ASPET

Membership in the Division for Toxicology is FREE if you are an ASPET member, and ASPET provides funds to the Division based on its membership. These funds are used to support the Postdoc and Graduate Student Awards, and food at the mixers. While our Division is healthy, we always welcome new energy and ideas. You may join as many Divisions as you want. Please also encourage your students and postdocs to join ASPET and the Division for Toxicology. The first year of student membership is free, and dues thereafter are 25% of Regular member dues. Additional information regarding membership can be found  HERE

Predoctoral Award Winners at EB2008

Division for Toxicology Symposia at EB2010 Anaheim, April 24-28 (printable version is HERE

Symposium 1: Regulating the Regulators: Redox regulation and stress response proteins

Co-Sponsor: Division for Drug Metabolism

Chair: Daret St. Clair

Cellular redox status (oxidizing/reducing conditions) is known to play several important roles in signaling of life and death processes. Transcription regulators are important targets of redox regulation that carry out the survival and death responses.  However, increasing evidence suggests that cellular redox status is also regulated by the activity of transcription factors and modifiers such as NF-kB, p53 and SIRT.  Hence, activation of these proteins and the subsequent alteration of cellular redox status are interrelated.  In light of these new findings, we believed that a topic on the connections between cellular redox status and redox sensitive proteins is timely and should be of importance to many scientists attending ASPET meetings. Given that cellular redox status contributes to almost all aspects of biological function, and transcription regulatory proteins are critical for normal cellular functions, this proposed session will serve as an excellent platform to bring together two important fields: redox and transcription regulation. 

Introduction to the connections between cellular redox status and transcription responses

Daret St. Clair, PhD, Department of Toxicology, University of Kentucky

p53 regulates mitochondrial function

Paul M. Hwang, MD, PhD, Cardiology Branch, National Heart, Lung, and Blood Institute, NIH

ROS and p53 modulators in cancer specific apoptosis

Sam Lee, PhD, Cutaneous Biology Research Laboratory, Harvard Medical School

SIRT3 is a mitochondrial tumor suppressor gene required for maintenance of mitochondrial integrity and oxidative metabolism during stress

David Gius, MD, PhD, Radiation Oncology Branch, NIH

Mitochondria: novel regulators of the Keap1/Nrf-2antioxidant pathway

Aimee Landar, PhD, Center for Free Radical Biology, University of Alabama-Birmingham

(Young Investigator Speaker)

The bi-directional role of p53 on MnSOD expression

Sanjit Dhar, PhD, Graduate Center for Toxicology, University of Kentucky

(Young Investigator Speaker)

Symposium 2: Role of mitochondria in pathogenesis of drug hepatotoxicity

Co-Sponsor: Division for Drug Metabolism & Division for Integrative Systems, Translational and Clinical Pharmacology

Chair: Neil Kaplowitz

Mitocondria have attracted renewed interest because of their role in oxidative stress and as potential target to toxic drugs. Drugs that interfere with electron transport promote ROS production. Critical in handling this oxidative stress is the status of the mitochondrial defense and its compartmentation. The eventual exhaustion of this defense exposes the cytoplasm to ROS.  The effect on sustained activation of signal transduction pathways may then lead to JNK targeting to mitochondria and cell death. The discussion of this area of research will bring attention to the importance of mitochondria as a primary and secondary target of hepatotoxic drugs. This will stimulate discussion and more work to advance the field of hepatotoxicity.

Introduction

Neil Kaplowitz, MD, Division of Gastroenterology and Liver Diseases, University of Southern California

Compartmentation of oxidative stress defense in mitochondria: implications for drug toxicity

This talk will address the role of mitochondrial thioredoxin and GSH and its relation to other compartments

Dean Jones, PhD, Division of Ophthalmology, Emory University School of Medicine

Mitochondrial permeability transition

This talk will focus on the MPT, what regulates it and its contribution

John LeMasters, MD, PhD, Department of Biochemistry and Molecular Biology and Pharmaceutical Sciences

Medical University of Southern Carolina

Interplay of signal transduction and mitochondria in the acetaminophen model

This talk will address role of kinases (JNK, etc) in mediating oxidative stress induced necrosis

Derick Han, PhD, Division of Gastrointestinal and Liver Diseases, University of Southern California

(Young Investigator Speaker)

Threshold for mitochondrial participation in idiosyncratic DILI

This talk will address the SOD+/- in increasing or unmasking of drugs and mechanisms

Urs Boelsterli, PhD, Department of Pharmaceutical Sciences, University of Connecticut School of Pharmacy

Symposium 3: Div Tox-sponsored symposium: ABC transporters, their role in physiology, toxicology and cancer

Chair: John Schuetz

            Details are being finalized

 

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