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
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  BulletDr. DeFrances
  BulletDr. Delude
  BulletDr. Demetris
  BulletDr. Dong
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  BulletDr. Gandhi
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  BulletDr. Gnarra
  BulletDr. Grandis
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  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. Zarnegar


V-line Dr. Luo
Jianhua Luo, Associate Professor
MD, Guangzhou Medical Institute, Canton, China, 1982
PhD, University of Maryland at Baltimore, MD, USA, 1992
Email:  luojh@pitt.edu


Completion of human genome sequencing laid down the foundation for genome-wide analysis of gene expression in human malignancies. In order to understand the pathogenesis of prostate cancer, it is necessary to identify which set of the estimated 30,000 to 40,000 genes in the human genome involving in the development of the disease. Application of high throughput, quantitative analysis of gene expression in human cancer samples appears to be the most logical and conventional way to obtain information of gene expression alterations in human cancer, and help to identify critical genetic event triggering the irreversible process of malignancy. In the past three years, we have been utilizing two important technologies to study genetic alterations in prostate cancer, i.e. Affymetrix's oligo chip array and differential subtraction chain developed from this laboratory.

Despite high incidences of prostate cancer among men in the United States, only a small fraction of prostate cancer develops life-threatening conditions. Recently, using differential subtraction chain, we identified two novel genes whose alteration might be associated with progression of prostate cancer. Currently, we are focusing on investigating physiological role of one of these genes, myopodin, and its mechanism that mediates metastasis suppression activity. By performing large scale Affymetrix chip analysis, we identify a set of genes whose expression alterations dictate the aggressive behavior of prostate cancer. Preliminary random blind test suggest that this set of genes is a fairly reliable outcome predictor. Larger clinical test is underway to determine possible clinical usage of this gene profile predictor.

Recent Publication

  1. Yan P. Yu, Guoying Yu, George Tseng, Kathleen Cieply, Joel Nelson, Marie Defrances, Reza Zarnegar, George Michalopoulos and Jian-Hua Luo (2007). Glutathione Peroxidase 3, Deleted or Methylated In Prostate Cancer, Suppresses Prostate Cancer Growth and Metastasis. Cancer Research, in press.
  2. Baoguo Ren, Yan P. Yu, George C. Tseng, Chuanyue Wu, Ka Chen, Uma N. Rao, Joel Nelson, George K. Michalopoulos and Jian-Hua Luo (2007). Analysis of Integrin ¦Á7 Mutations in Prostate Cancer, Liver Cancer, Glioblastoma Multiforme, and Leiomyosarcoma. Journal of National Cancer Institute, 99, 868-880.
  3. Craig, F.E., Johnson, L.R., Harvey, S.A.K., Nalesnik, M.A., Luo, J.H., Bhattacharya, S.D., and Swerdlow, S.H. (2007). Gene Expression Profiling of Epstain-Bar Virus-Positive and Negative Monomorphic B-Cell Post-transplant Lymphoproliferative Disorders. Diagnostic Molecular Pathology, in press
  4. Shirish Paranjpe, William C. Bowen, Aaron W. Bell, Kari Nejak-Bowen, Jian-Hua Luo and George K. Michalopoulos (2007). Cell cycle effects caused by inhibition of HGF and its receptor c-met in regenerating rat livers by RNA interference. Hepatology 45, 1471-1477.
  5. Chiosea S, Jelezcova E, Chandran U, Luo J, Mantha G, Sobol RW, Dacic S. (2007). Overexpression of Dicer in precursor lesions of lung adenocarcinoma. Cancer Res. 67(5):2345-50.
  6. Yingjian Li, Junwei Yang, Jian-Hua Luo, Shoukat Dedhar and Youhua Liu (2007). Tubular epithelial cells dedifferentiation is driven by helix-loop-helix transcriptional inhibitor Id1. Journal of American Society of Nephrology 18, 449-60.
  7. Jian-Hua Luo, Baoguo Ren, Sergei Keryanov, George C. Tseng, Uma N.M. Rao, Satdarshan P. Monga, Steven Strom, Anthony J. Demetris, Michael Nalesnik, Yan P. Yu, Sarangarajan Ranganathan and George K. Michalopoulos (2006). Transcriptomic and Genomic analysis of Human Hepatocellular Carcinomas and Hepatoblastomas. Hepatology 44, 1012-1024.
  8. Yan Ping Yu and Jian-Hua Luo (2006). Myopodin Mediated Suppression of Prostate Cancer Cell Migration Involves Interaction with Zyxin. Cancer Research, 66, 7414-7419.
  9. Yan Ping Yu, George C. Tseng and Jian-Hua Luo (2006). Inactivation of Myopodin Expression Is Associated with Prostate Cancer Relapse. Urology 68, 578-82.
  10. Guoying Yu, George C. Tseng, Yan Ping Yu, Tim Gavel, Joel Nelson, Alan Wells, George Michalopoulos, Demetrius Kokkinakis and Jian-Hua Luo (2006). CSR1 Suppresses Tumor Growth and Metastasis of Prostate Cancer. American Journal of Pathology 168, 597-607.
  11. Baoguo Ren, Guoying Yu, George C. Tseng, Kathleen Cieply, Timothy Gavel, Joel Nelson, George Michalopoulos, Yan Ping Yu and Jian-Hua Luo (2006). MCM7 Amplification and Overexpression Are Associated with Prostate Cancer Progression. Oncogene 25, 1090-1098.



 

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