Cellular and Molecular Pathology (CMP)
Graduate Training Program
 

Faculty and Their Research Interests

   Faculty Index

  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. Delude
  BulletDr. Demetris
  BulletDr. Dong
  BulletDr. Donnenberg
  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. Monga
  BulletDr. Mars
  BulletDr. Michalopoulos
  BulletDr. Ochoa
  BulletDr. O'Keefe
  BulletDr. Oltvai
  BulletDr. Oury
  BulletDr. Pflug
  BulletDr. Piganelli
  BulletDr. Saunders
  BulletDr. Shapiro
  BulletDr. Stolz
  BulletDr. Strom
  BulletDr. Surti
  BulletDr. Vodovotz
  BulletDr. Wang
  BulletDr. Wells
  BulletDr. Wenzel
  BulletDr. Wiley
  BulletDr. Wu
  BulletDr. Yin
  BulletDr. Yu
  BulletDr. Zarnegar

V-line Dr. Bostwick
Jean J. Latimer, Assistant Professor
PhD, Roswell Park Cancer Institute
State University of NY
Email: latimerj@pitt.edu, latimerjj@upmc.edu
HomePage: http://www.upci.upmc.edu/labs/latimer/index.html



Research Interests:

Dr. Jean Latimer's laboratory is engaged in human breast tissue engineering and breast cancer research. Her laboratory has developed a novel method of establishing long lived primary cultures from non-diseased breast tissue as well as breast tumors (stages 0-IV). From these robust primary cultures her laboratory has created over 100 cell lines without the use of exogenously transforming agents.

Dr. Latimer's laboratory is using this unique tissue engineering methodology to investigate the role of Nucleotide Excision Repair in Breast Cancer etiology. In addition her most recent funding is to determine how stem cells in the breast may contribute to racially disparate types of breast cancer.

Grants:

"Biomarkers of invasiveness in racially disparate populations using an isogenic and progressive model of human DCIS"
Principal Investigator: Latimer, J.J.
Agency: Komen for the Cure
Period: May 1, 2007-April 31, 2009
The major aim of this grant is to use 3 unique DCIS (and matching contralateral breast) cell lines to establish biomarkers of pre-invasive breast cancer aggressivenss using expression microarray technology and xenograft mice.

"Quantitative proteomics of nuclear matrix proteins in novel human ductal carcinoma in situ model systems"
Principal Investigators: (Day,B. and Latimer, J.J.)
Agency: Department of Defense (synergy award) ($700,000)
Period: Dec. 1, 2008-Nov. 31, 2010
The major aim of this grant is to test the hypothesis that detectable differences exist between invasive and noninvasive DCIS at the protein level, particularly in the nucleus, and these differences are distinct from those demonstrated at the nucleic acid level.

Recent Publications

Grant, S.G., Das, R., Cerceo, C.M., Rubinstein, W.A., Latimer, J.J. (2007) Elevated levels of somatic mutation in a manifesting BRCA1 mutation carrier. Pathology Oncology Research, in press.

Donovan, M., Miles, T.D., Latimer, J.J., Grant, S.G. Talbott, E., Sasco, A.J., and Davis, D.L. (2006) Association between biomarkers of environmental exposure and increased risk of breast cancer. Nature Rev. Cancer 6: c1

Rubinstein, W.S., Latimer, J.J., Sumkin, J., Huerbin, M.B.. Grant, S.G. and, Vogel, V. G. (2006) Prospective screening study of 0.5 Tesla dedicated magnetic resonance imaging for the detection of breast cancer in young high-risk women, BMC WomenĄŻs Health 6(10) online.

Donovan, M., Miles, T.D., Latimer, J.J., Grant, S.G. Talbott, E., Sasco, A.J., and Davis, D.L. (2006) Association between biomarkers of environmental exposure and increased risk of breast cancer. Nature Rev. Cancer 6: c1.

Kelly, C.M. and Latimer, J.J. (2005) Unscheduled DNA synthesis: a functional assay for global genomic nucleotide excision repair. Methods in Molecular Biology 291: 303-320.

Johnson, J.M., and Latimer, J.J. (2005) Analysis of DNA repair using transfection-based host cell reactivation. Methods in Molecular Biology 291: 321-335.

Latimer, J.J., Rubinstein, W.S., Johnson, J.M., Kanbour-Shakir, A., Vogel, V.G., and Grant, S.G. (2005) Haploinsufficiency for BRCA1 is associated with normal levels of DNA nucleotide excision repair in breast tissue and blood lymphocytes. BMC Medical Genetics 6: 26.

Latimer, J.J., Nazir, T., Flowers, L.C., Forlenza, M.J., Beaudry-Rodgers, K., Kelly, C.M., Conte, J.A., Shestak, K., Kanbour-Shakir, A., Grant, S.G. (2003) Unique tissue-specific level of DNA nucleotide excision repair in primary human mammary epithelial cultures. Experimental Cell Research 291:111-121.

Draper, D., Kush, M.J., Donohoe, W., Janosky, J., Latimer, J.J., Heine R.P. (2001) Preterm premature rupture of membranes (pPROM) without labor is not associated with increased levels of matrix metalloproteinase-9 (MMP-9) protein. Prenatal and Neonatal Medicine 6:1-8.

Grant, S.G., Wenger, S.L., Latimer, J.J., Thull D, Burke, L.W. (2000) Analysis of genomic instability using multiple assays in a patient with Rothmund-Thomson syndrome. Clinical Genetics 58:209-215.

Forlenza, M., Latimer, J.J., Baum, A. (2000) The effects of stress on DNA repair capacity. Psychology & Health 15:881-891



 

University of Pittsburgh
School of Medicine