Cellular and Molecular Pathology (CMP)
Graduate Training Program
 

Faculty and Their Research Interests

   Faculty Index

  BulletDr. Badylak
  BulletDr. Barak
  BulletDr. Becich
  BulletDr. D. Becker
  BulletDr. J. Becker
  BulletDr. Billiar
  BulletDr. Blair
  BulletDr. Bostwick
  BulletDr. Bowser
  BulletDr. Chaillet
  BulletDr. Chang
  BulletDr. Cheng
  BulletDr. Chu
  BulletDr. Clemens
  BulletDr. DeFrances
  BulletDr. Demetris
  BulletDr. Dong
  BulletDr. Donnenberg
  BulletDr. Duensing
  BulletDr. Fox
  BulletDr. Gandhi
  BulletDr. Giannoukakis
  BulletDr. Gnarra
  BulletDr. Grandis
  BulletDr. Hackam
  BulletDr. Hebda
  BulletDr. Huard
  BulletDr. Kaminski
  BulletDr. Katyal
  BulletDr. Kelavkar
  BulletDr. Klunk
  BulletDr. Kulich
  BulletDr. Lagasse
  BulletDr. Latimer
  BulletDr. Luyuan Li
  BulletDr. Yong Li
  BulletDr. Youhua Liu
  BulletDr. Lokshin
  BulletDr. Luo
  BulletDr. Lyons-Weiler
  BulletDr. Mars
  BulletDr. Michalopoulos
  BulletDr. Monga
  BulletDr. Nikiforov
  BulletDr. O'Keefe
  BulletDr. Oltvai
  BulletDr. Oury
  BulletDr. Piganelli
  BulletDr. Robinson
  BulletDr. Rubin
  BulletDr. Saunders
  BulletDr. Shapiro
  BulletDr. Stolz
  BulletDr. Strom
  BulletDr. Surti
  BulletDr. Vodovotz
  BulletDr. Vorp
  BulletDr. Wang
  BulletDr. Wells
  BulletDr. Wenzel
  BulletDr. Wiley
  BulletDr. Wu, C
  BulletDr. Yin
  BulletDr. Yu
  BulletDr. Zarnegar




V-line
Dorothea Becker, Ph.D.,  Professor
Ph.D., Free University of Berlin, Berlin, Germany, 1977
E-mail: dbecker@pitt.edu

Dr. Becker's Laboratory Website

The overall objective of the research conducted in my lab concerns the characterization of genes that govern the onset and progression of human neoplasia. Given this goal, my lab focuses upon human melanoma and its precursor lesions as a model. Using molecular approaches in combination with optical imaging, three major projects are pursued. First, determination of the role of basic fibroblast growth factors (FGF2) and fibroblast growth factor receptor 1 (FGFR-1) in melanoma proliferation and angiogenesis. Second, characterization of cell adhesion molecules that are involved in melanoma invasion and metastasis. Third, analysis of new genes, identified by SAGE and DNA microarrays that are expressed in early and advanced-stage melanomas and/or melanoma precursor lesions.

Recent Publications

Moschos, S. J., Pfaff Smith, A., Mandic, M., Athanassiou, C., Watson-Hurst, K., Jukic, D. M, Edington, H. D., Kirkwood, J. M., and Becker, D. (2007). SAGE and antibody array analysis of melanoma-infiltrated lymph nodes: identification of Ubc9 as an important molecule in advanced-stage melanomas. Oncogene 26: 4216-4225.

Watson-Hurst, K., and Becker, D. (2006). The role of N-cadherin, MCAM, and ¦Â3 Integrin in melanoma proliferation, migration, and invasion. Cancer Biol. Ther. 5: 1375-1382.

Smith, A. P. Hoek, K. and Becker, D. (2005). Whole-genome expression profiling of the melanoma progression pathway reveals marked molecular differences between nevi/melanoma in situ and advanced-stage melanomas. Cancer Biol. Ther. 4: 1018-1029.

Pfaff Smith, A., Weeraratna, A. T., Spears, J. R., Meltzer, P. S. and Becker, D. (2004). SAGE identification and fluorescence imaging analysis of genes and transcripts in melanomas and precursor lesions. Cancer Biol. Ther. 3: 104-109.

McDonald, S., Edington, H. D., Kirkwood, J. M. and Becker, D. (2004). Gene expression profiling of VGP melanomas and MGP melanoma-positive lymph nodes. Cancer Biol. Ther. 3: 110-120.



 

University of Pittsburgh
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