MICROENVIMET : SEVENTH FRAMEWORK PROGRAM
MICROENVIMET : SEVENTH FRAMEWORK PROGRAM

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Partner 9
B. Turk and O. Vasiljeva – JSI - Ljubljana (SI)

http://www.ijs.si/

Qualifications and capacity:
The Department of Biochemistry, Molecular and Structural Biology is one of the most active institutions in the field of the papain-like cysteine proteases and their endogenous inhibitors. Research interests encompass different aspects of molecular and cellular biology, structural biology, physiology, and biomedical applications (cancer, inflammation, immunology).

Boris Turk (PhD) is Head of the Department and Associate Prof. of Biochemistry at University of Ljubljana. He has expertise in protease biochemistry and in apoptosis, where he is involved in studies of apoptosis resistance of cancer cells. He is currently involved in two EU FP6 projects NANOSAFE2 (NMP2-CT-2005-515843) and CAMP (Chemical Genomics by Activity Monitoring of Proteases; LSHG-CT-2006-018830).
Olga Vasiljeva (MD, PhD) has broad experience and knowledge in the field of proteases and their inhibitors. She has gained expertise in transgenic tumour models during her postdoctoral training at the Department of Molecular Medicine and Cell Research Freiburg, Germany. She contributed to demonstrate the importance of tumour and stromal cells derived cysteine proteases for tumour progression and metastasis. Her scientific interests are focused on the investigation of the role of cysteine cathepsin inhibitors in metastatic dissemination by studying the tumour-host interactions both at primary and secondary sites. She is a promising young scientist establising her own group.

Most relevant publications:
Inhibition of papain-like cysteine proteases and legumain by caspase-specific inhibitors: when reaction mechanism is more important than specificity.
Rozman Pungercar J, Kopitar-Jerala N, Bogyo M, Turk D, Vasiljeva O, Klemencic I, Vandenabeele P, Bromme D, Puizdar V, Fonovic M, Trstenjak-Prebanda M, Dolenc I, Turk V and Turk B
Cell Death Differ, 10: 881-888, 2003

Selective disruption of lysosomes in HeLa cells triggers apoptosis mediated by cleavage of bid by multiple papain-like lysosomal cathepsins.
Cirman T, Oresic K, Droga-Mazovec G, Turk V, Reed JC, Myers RM, Salvesen GS and Turk B
J Biol Chem, 279: 3578-3587, 2004

Tumour cell–derived and macrophage-derived cathepsin B promotes progression and lung metastasis of mammary cancer.
Vasiljeva O, Papazoglou A, Kruger A, Brodoefel H, Korovin M, Deussing J, Augustin N, Nielsen BS, Almholt K, Bogyo M, Peters C and Reinheckel T
Cancer Res, 66: 5242-5250, 2006

Targeting proteases: successes, failures and future prospects.
Turk B
Nature Reviews Drug Discovery, 5: 785-799, 2006

Emerging roles of cysteine cathepsins in disease and their potential as drug targets.
Vasiljeva O, Reinheckel T, Peters C, Turk D, Turk V and Turk B
Curr Pharm Des, 13(3): 385-401, 2007







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