Updated March, 2013


S. Perwez Hussain, Ph.D.
Tenure Track Investigator

Biography: Dr. Hussain received his Ph.D in Cancer Biology from Jawaharlal Nehru University, New Delhi, India. He was then trained as a Post Doctoral Fellow at Swiss Institute for Research on Cancer, Lausanne, Switzerland and subsequently at the Laboratory of Human Carcinogenesis, National Cancer Institute (NCI), Bethesda, Maryland. He then joined faculty at the University of Maryland School of Medicine, Baltimore. He was recruited to NCI as a tenure track investigator in 2009. He has published over 70 peer-reviewed manuscripts and book chapters and frequently invited to speak at national and international scientific conference. He also serves on many scientific committee and editorial boards for cancer journals.

Research Program and Goals:

Our research program investigates the molecular pathogenesis of pancreatic cancer to determine molecular events critical to tumor progression, using an integrative biology translation research approach. Pancreatic cancer is one of the most lethal malignancies with a median survival of 6 months and a 5-year survival of mere 6%. The dismal prognosis in pancreatic cancer is due to the lack of an effective therapy and reliable biomarkers for early diagnosis. Understanding pancreatic tumor biology, a priority recommendation of the Pancreatic Cancer Progress Review Group (convened by NCI), is essential to develop strategies for prevention, diagnosis and effective therapeutic intervention. The Pancreatic Cancer Unit (PCU) investigates pancreatic tumor biology with focus on the role of inflammatory mediators, to understand the underlying mechanism of tumor progression, and to identify candidate targets for therapeutic intervention. Our efforts include both a focused and global approach, which involves the analyses of clinical samples to assess the biological relevance of a marker (e.g., gene or metabolite) by evaluating its association with disease aggressiveness in pancreatic cancer patients, followed by the investigation of its mechanistic role in disease progression using pancreatic cancer cells and genetically engineered mouse model of pancreatic cancer. The overall aim of our research program is to understand the pancreatic tumor biology and identify critical pathways associated with tumor progression and disease aggressiveness that can be targeted for therapeutic intervention.

Current Research Projects:

1. Role of Immune and Inflammatory mediators in the progression of pancreatic cancer

Evidence from epidemiological and molecular studies support a role of inflammation in the development, progression and therapeutic resistance in pancreatic cancer. One such evidence comes from the observation that the risk of developing pancreatic cancer increases several-fold, in patient with hereditary and sporadic pancreatitis. There is a step-wise accumulation of inflammatory changes during the development of PDAC, intermingled within a characteristic desmoplastic stroma. Increase in the level of cytokines, chemokines, generation of reactive oxygen and nitrogen species, alteration in inflammation-associated miRNA expressions, and induction of NF-kB are some of the major inflammation-mediated events that may contribute to the development and progression of cancer. Many of the immune and inflammatory mediators are expressed both in tumor epithelial and stromal cells. However, the precise roles of inflammatory and immune mediators in the progression and aggressiveness of pancreatic cancer are not completely understood. Defining the mechanistic role of these mediators in disease progression may help identify candidate therapeutic targets. We have recently shown that an increased expression level of macrophage migration inhibitory factor (MIF), a proinflammatory cytokine, in tumors was significantly associated with poor outcome in resected cases of PDAC, induced epithelial-to- mesenchymal transition and enhanced tumor growth and metastasis (Funamizu et. al., Int J. Cancer, 2012). We are currently exploring, if MIF and other inflammatory mediators are candidate therapeutic targets in pancreatic cancer.

2. Molecular Profiling of Human Pancreatic Cancer:

Molecular profiling using genomic, transcriptomics and metabolomics, collectively known as “OMICS”, is an important and widely used strategy for an unbiased, global screening of molecular characteristics and/or differences in biological samples, which may help in understanding the biological mechanisms, which contribute to the development and progression of cancer. The highly heterogeneous characteristic of pancreatic tumor underscores the significance of a comprehensive and integrative molecular profiling in larger cohort of tumor, followed by their validations in multiple independent cohorts and assay platforms to examine molecular subgroups, and understand how several molecular events are intertwined as a network leading to the disease aggressiveness and poor outcome. The delineation of subtypes-specific biology and critical pathways associated with disease outcome may identify subtype-specific candidate targets for therapeutic intervention. Our overall goal is to examine a large sample set of PDAC, using global strategies, including transcriptomics and metabolomics to 1) identify critical genes and pathways that may be interrogated as candidate therapeutic targets; 2) Distinguish molecular subgroups with distinct therapeutic response and disease outcome; 3) Molecular characterization of early stage tumors with extreme prognoses to reveal critical pathways linked to outcome.

Selected Recent References

1. Zhang G, Schetter A, He P, Funamizu N, Gaedcke J, Ghadimi BM, Ried T, Hassan R, Yffantis HG, Lee DH, Lacy C, Maitra A, Hanna N, Alexander HR, Hussain SP: DPEP1 inhibits tumor cell invasiveness, enhances chemosensitivity and predicts clinical outcome in pancreatic ductal adenocarcinoma. PLoS One, 7 (2), e31507, 2012.

2. Funamizu N, Hu C, Lacy C, Schetter A, Zhang G, He P, Gaedcke J, Ghadimi BM, Ried T, Yffantis HG, Lee DH, Subleski J, Chan T, Weiss JM, Back TC, Yanaga K, Hanna N, Alexander HR, Maitra A, Hussain SP: Macrophage Migration Inhibitory Factor (MIF) induces epithelial to mesenchymal transition, enhances tumor aggressiveness and predicts clinical outcome in resected pancreatic ductal adenocarcinoma. Int. J. Cancer, July 23, Epub 2012.

3. Mathe, E., Nguyen, G., Funamizu, N., He, P., Make, M., Croce, C.M and Hussain, S.P: Inflammation regulates micron expression in cooperation with p53 and nitric oxide. Int. J. Cancer, 131, 760-765, 2012.

4. Okayama, H., Saito, M., Oue, N., Weiss, J.M., Stauffer, J., Takenoshita, S., Wiltrout, R.H., Hussain, S.P, Harris CC: NOS2 enhances KRAS-induced lung carcinogenesis, inflammation and microRNA-21 expression. Int. J. Cancer, May 23, Epub, 2012.

5. Du, Q., Park, K. S., Guo, Z., He, P., Nagashima, M., Shao, L., Rohit Sahai, Geller, D.A and Hussain, S.P.: Regulation of human NOS2 expression by Wnt-≤-catenin signaling. Cancer Research, 66: 7024-7031, 2006.


E-mail address: hussainp@mail.nih.gov

[Home] | [Office of the Chief] [MG&C Section] | [ME Section] [Liver Carcinogenesis Unit] |[Pancreatic Cancer Unit]
[Complete Bibliography] | [Post Doctoral Opportunities]