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Craig D. Logsdon, Ph.D.

Present Title & Affiliation

Primary Appointment

Professor, Department of Cancer Biology, The University of Texas M. D. Anderson Cancer Center, Houston, TX

Dual/Joint/Adjunct Appointment

Professor, Department of Gastrointestinal (GI) Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX

Research Interests

The goal of my laboratory is to improve the diagnosis and treatment of pancreatic cancer and the related disease pancreatitis. One of our major goals is the identification of disease specific molecules useful as biomarkers or therapeutic targets. For this purpose we have utilized gene profiling and proteomics approaches to identify disease specific molecules. These molecules are then verified as being cancer cell specific using real-time quantitative PCR, Western blotting and immunolocalization in tissue arrays. Functional characterization is then conducted  in order to identify molecules with high potential for translational value such as those involved in cancer cell proliferation and survival. Validation of functional roles is conducted  intially in vitro and then in vivo. In vitro experiments are conducted both by over-expression and reduced-expression. Molecules that increase pancreatic cancer aggressiveness when over-expressed and which decrease pancreatic cancer cell growth when silenced may be good targets for therapeutic intervention. Once an important functional molecule is identified we develop experimental therapeutics using reagents developed or identified for manipulation of these molecules. Antibodies, dominant negatives, siRNAs and pharmacological agents capable of manipulating the function of the molecules are tested as potential therapeutic agents in animal models. Currently, we are using orthotopically transplanted pancreatic cancer cells or primary xenografts placed in immune deficient animals as our models. We are also developing genetic animal models for pancreatic cancer. Using these approaches  we have already discovered important biomarkers and exciting candidates for therapeutic intervention. However, there are many more candidate molecules to investigate and much more to discover. This is a very exciting time for research into pancreatic disease with many opportunities for collaborative research.

Office Address

The University of Texas M. D. Anderson Cancer Center
Department of Cancer Biology
1515 Holcombe Blvd.
Unit Number: 953
Houston, TX 77030
Room Number: 2SCR2.2014
Phone: 713 563-3585
Fax: 713-563-8986
Email: clogsdon@mdanderson.org

Education & Training

Degree-Granting Education

1981 University of California, Berkeley, CA, PHD, Physiology

Experience/Service

Endowed Positions

Lockton Distinguished Chair for Pancreatic Cancer Research, The University of Texas M. D. Anderson Cancer Center, Houston, TX, 2004-present

Honors and Awards

2007 President, American Pancreatic Association
1981 Phi Beta Kappa Member
1979 Julius T. Hansen Memorial Prize for Outstanding Graduate Student
1977 University of California Regents Fellow, University of California, Berkeley
1976 Suma Cum Laude, California State University, Humboldt
1976 University of California Regents Fellow, University of California, Berkeley

Selected Publications

Peer-Reviewed Original Research Articles

1. Ji B, Tsou L, Wang H, Gaiser S, J Daniluk J, DZ Chang, Y Bi, T Grote, DS Longnecker, and CD Logsdon. Ras Activity Levels Control the Development of Pancreatic Diseases. Gastroenterology. e-Pub 6/2009. PMID: 19501586.
2. Arumugam T, Ramachandran V, Rournier KF, H Wang, Marquis L, Abbruzzese JL, Gallick GE, Logsdon CD, McConkey DJ, Choi W. Epithelial to Mesenchymal Transition Contributes to Drug Resistance in Pancreatic Cancer. Cancer Res 69(14):5820-8, 2009. PMID: 19584296.
3. Ji B, Gaiser S, Chen X, Ernst SA, and CD Logsdon. Intracellular trypsin induces pancreatic acinar cell death but not NFkB activation. Journal of Biological chemistry 284(26):17488-98, 2009. PMCID: PMC19383608.
4. Wang, L, Heidt DG, Lee CJ, Yang H, Logsdon CD, Zhang L, Fearon ER, Ljungman M, Simeone DM. Oncogenic Function of ATDC (TRIM29) in Pancreatic Cancer Through Wnt Pathway Activation and B-catenin Stabilization. Cancer Cell, 2009. PMCID: PMC2673547.
5. Wang H, Song X, Logsdon C, Zhou G, Evans DB, Abbruzzese JL, Hamilton SR, Tan TH, Wang H. Proteasome-mediated degradation and functions of hematopoietic progenitor kinase 1 in pancreatic cancer. Cancer Res. 69(3):1069-70, 2009. PMID: 19141650.
6. Ji B, Song J, Tsou L, Bi Y, Mortensen R, Logsdon CD. BAC Recombineering Allows Development of an Efficient Pancreatic Acinar Cell Specific Transgenic Model. Genesis 46(8):390-395, 8/2008.
7. Ramachandran V, Arumugam T, Wang H, Logsdon CD. Anterior Gradient 2 (AGR2) is Expressed and Secreted During the Development of Pancreatic Cancer and Promotes Cancer Cell Survival. Cancer Research 68(19):7811-1818, 2008. PMID: 18829536.
8. Tong Z, Kunnumakkara AB, Wang H, Matsuo Y, Diagaradjane P. Harikumar KB, Ramachandran V, Sung B, Chakraborty A, Bresalier RS, Logsdon C, Aggarwal BB, Krishnan S, Guha S.. Neutrophil gelatinase-associated lipocalin: a novel suppressor of invasion and angiogenesis in pancreatic cancer. Cancer Res 65(15):6100-6108, 2008. PMCID: PMC2714276.
9. Pan X, Arumugam T, Yamamoto T, Levin PA, Ramachandran V, Ji B, Lopez-Berestein G, McConkey D, Logsdon CD. NFkB p65/relA Silencing Induces Apoptosis and Increases Gemcitabine Effectiveness in a Subset of Pancreatic Cancer Cells. Clin. Cancer Res. 14(4):8143-51, 2008. PMID: 19088029.
10. Grote T, Siwak DR, Fritsche HA, Joy C, Mills GB, Simeone D, Whitcomb DC, Logsdon CD. Reverse phase protein array for biomarkers in serum and plasma: Accurate detection of CA1909 in pancreatic cancer patient samples. Proteomics 8(15):3051-3060, 2008. PMID: 18615426.
11. Ji B, Song J, Tsou L, Bi Y, Mortensen R, Logsdon CD. Robust acinar cell transgene expression of CrErT via BAC recombineering. Genesis 46(8):390-395, 2008. PMID: 18693271.
12. Gray MJ, Van Buren G, Dallas NA, Xia L, Wang X, Yang AS, Somcio RJ, Lin YG, Lim S, Fan F, Mangala LS, Arumugam T, Logsdon CD, Lopez-Berestein G, Sood AK, Ellis LM. Therapeutic targeting of neuropilin-2 on colorectal carcinoma cells implanted in the murine liver. J Natl Cancer Inst 100(2):109-120, 2008. e-Pub 1/2008. PMID: 18182619.
13. Hwang RF, Moore T, Amos KD, Rivera A, Arumugam T, Ramachandran V, Evans DB, and Logsdon CD. Cancer-associated stromal fibroblasts promote pancreatic tumor progression. Cancer Res 68(3):918-926, 2007. PMCID: PMC2519173.
14. Simeone DM, Ji B, Banerjee M, Arumugam T, Li D, Anderson M, Bamberger AM, Greenson J, Brand RE, Ramachandran V, Logsdon CD. CEACAM1 is a serum biomarker for pancreatic cancer. Pancreas 34(4):436-443, 2007. PMID: 17446843.
15. Arumugam T, Ramachandran V, and Logsdon CD. Cromolyn Blocks S100P activation of RAGE and improves gemcitabine effectiveness in pancreatic cancer. J Natl Cancer Inst 98(24):1806-1818, 2006.
16. Arumugam T, Simeone DM, Schmidt AM, Logsdon CD. S100P stimulates cell proliferation and survival via receptor for activated glycation end products (RAGE). J Biol Chem 279:5059-5065, 2004. PMID: 14617629.
17. Okami J, Simeone DM, Logsdon CD. Silencing of the hypoxia-inducible cell death protein BNIP3 in pancreatic cancer. Cancer Res 64:5338-5346, 2004. PMID: 15289340.
18. Logsdon CD, Simeone DM, Binkley C, Arumugam T, Greenson JK, Giordano TJ, Misek DE, Kuick R, Hanash S. Molecular profiling of pancreatic adenocarcinoma and chronic pancreatitis identifies multiple genes differentially regulated in pancreatic cancer. Cancer Res 63:2649-2657, 5/2003. PMID: 12750293.

Grant & Contract Support

Title: Pancreatic Cancer Therapy Directed at RAGE and its Ligand S100P
Funding Source: The Linda de Picciotto Pancreas Cancer Research Program, The Marc Rich Foundation
Role: Principal Investigator
Duration: 10/1/2007 - 9/30/2012
 
Title: Molecular Mechanisms of Acute Pancreatitis
Funding Source: NIH/NIDDK
Role: Principal Investigator
Duration: 4/1/2007 - 3/31/2011

Last updated: 9/21/2009