
Masonic Cancer Center, University of Minnesota

Research Program: Tumor Biology and Progression
Professor, Departments of Laboratory Medicine and Pathology,Department of Urologic Surgery, and Otolaryngology — Head and Neck Surgery
ahmedk@umn.edu
612-467-2594 — office
612-467-2876 — lab
Preferred contact method: e-mail
Dr. Ahmed received his Ph.D. in Biochemistry in 1960 from McGill University, Montreal, Canada. He conducted postdoctoral studies in the laboratory of Dr. Jacob D. Judah at the Wistar Institute, University of Pennsylvania, Philadelphia, PA. He joined Masonic Cancer Center in 1994. He conducts research on signaling in abnormal and normal cell growth.
Signaling in Abnormal and Normal Cell Growth
The major focus of our research is to determine the molecular mechanisms that control cell growth, proliferation, and apoptosis. Our investigations are aimed at understanding the signaling in prostate cancer (PCa) and squamous cell carcinoma of the head and neck (SCCHN). Protein kinase CK2 (formerly casein kinase II or 2) is the biochemical paradigm for our studies. This protein kinase signal plays a critical role in cell growth and proliferation, and our recent work has also established it as a major modulator of the apoptotic activity in the cell. The importance of CK2 in cancer relates to the consistently observed dysregulation of this kinase in all the cancers that have been examined. The ability of CK2 to promote cell growth as well as suppress apoptosis links the kinase to cancer biology as cancer cells are characterized by dysregulation not only of proliferation but also of apoptosis. An important aspect CK2 is that this signal has the potential of serving as a target for inducing apoptosis in cancer cells. Current studies in our laboratory are focused on this aspect as well as on defining the mechanism of CK2 mediated suppression of apoptosis. Many of the CK2 functions related to cell growth and cell death are mediated via its signaling to the nuclear structures (such as chromatin and nuclear matrix). As such, we are interested in delineating the mechanism of these signaling events. Investigations in our laboratory have made the initial proof of principle observations on the potential targeting of CK2 for cancer therapy by antisense CK2 mediated molecular downregulation of CK2. A novel nanoparticle approach is also being developed for delivering the antisense specifically to the tumor cells in vivo. The experimental studies in the laboratory employ diverse range of biochemical, cell biological, and molecular biological techniques.
Unger GM, Davis AT, Slaton JW, Ahmed K: Protein kinase CK2 as regulator of cell survival: Implications for cancer therapy. Curr Canc Drug Targets 4(1): 77-84, 2004.
Wang G, Davis AT, Ahmed K: Suppression of receptor-mediated apoptosis by CK2. Second Messengers and Phosphoprotein Signaling. Proceedings of the 12th International Conference on Second Messengers and Phosphoproteins, Montreal, Canada, 2004. pp 209-212.
Patel A, Miller L, Ahmed K, Ondrey F: NF-B downregulation strategies in head and neck cancer treatment. Otolaryngol Head Neck Surg 131: 288-295, 2004.
Slaton JW, Sloper DT, Unger G, Davis A, Ahmed K: Induction of apoptosis by antisense CK2 in human prostate cancer xenograft model. Mol Canc Res 2: 712-721, 2004.
Wang G, Unger G, Ahmad KA, Slaton JW, Ahmed K: Downregulation of CK2 induces apoptosis in cancer cells—A potential approach to cancer therapy. Mol Cell Biochem 274: 77-84, 2005.
Ahmad KA, Wang G, Ahmed K. Intracellular hydrogen peroxide production is an upstream event in apoptosis induced by down-regulation of casein kinase 2 in prostate cancer cells. Mol Cancer Res. 2006;4:331-338.
Wang G, Ahmad KA, Unger G, Slaton JW, Ahmed K. CK2 signaling in androgen-dependent and -independent prostate cancer. J Cell Biochem 99: 382-391, 2006.
Kramerov AA, Saghizadeh M, Pan H, Kabosova A, Montenarh M, Ahmed K, Penn JS, Chan CK, Hinton DR, Grant MB, Ljubimov AV: Expression of protein kinase CK2 in astroglial cells of normal and neovascularized retina. Amer J Path 168: 1722-1736, 2006.
Wang G, Ahmad KA, Ahmed K: Role of CK2 in regulation of TRAIL induced apoptosis in prostate cancer cells. Canc Res 66: 2242-2249, 2006.
He H, Tan M, Pamarthy D, Ahmed K, Sun Y: CK2-mediated phosphorylation of SAG at Thr 10 regulates its stability but not its E3 ligase activity. Mol Cell Biochem 295: 179-188, 2007.
Ahmad KA, Harris NH, Johnson AD, Lindvall HCN, Wang G, Ahmed K: Protein kinase CK2 modulates apoptosis induced by resveratrol and EGCG in prostate cancer cells. Mol Canc Therap 6: 1006-1012, 2007.
McDonnell MA, Abedin MJ, Melendez M, Platikanova TN, Ahmed K, Kelekar A: Phosphorylation of murine Caspase-9 by the protein kinase CK2 regulates its cleavage by Caspase-8. J Biol Chem 283: 20149-20158, 2008.
Ahmed K, Issinger O-G, Meggio F, Pinna LA: CK2 in Health and Disease—Preface. Mol Cell Biochem 316: 1-3, 2008.
Ahmad KA, Wang G, Unger G, Slaton J, Ahmed K: Protein kinase CK2—A key suppressor of apoptosis. Adv Enzyme Regul 48: 179-187, 2008.
Wang G, Ahmad KA, Ahmed K: Impact of protein kinase CK2 on inhibitor of apoptosis proteins (IAPs) in prostate cancer cells. Mol Cell Biochem 316: 91-97, 2008
Trembley JH, Wang G, Unger G, Slaton J, Ahmed K: CK2—A key player in cancer biology. Cell Mol Life Sci. 2009 Apr 24. [Epub ahead of print]