Gene regulatory networks in cancer
 Developing
new cancer therapies or diagnostic tests relies on our comprehension of
the molecular switches regulating the progress of cancer. Although
advances have been made recently our knowledge about these molecular
switches remains incomplete. A new approach to understanding cancer
progression is to construct gene regulatory networks for specific cell
types. Gene regulatory networks are constructed from high-quality gene
array data from hundreds of disruptant and/or time-course experiments
in cultured cells. Gene regulatory networks are best described as
circuit diagrams showing cause and effect relationships between many
signalling molecules within cells. They ultimately identify master
regulators of gene expression represented by network ‘hubs’ from which
numerous signals emanate.
We are combining novel methods
developed in our group with existing published methods for analysing
gene expression data and applying them to data in breast, skin and
colon cancer to uncover potential targets for investigation in the
laboratory. Moreover, we are combining clinical information such as
patient history, survival record, tumor grade and patient age, with
molecular data to improve the predictive power of our approach.
Key Publications:
J.
Srividhya, M.A. Mourão, E.J. Crampin,
S. Schnell
Enzyme
catalyzed reactions: from experiments to computational mechanism
reconstruction
Computational
Biology & Chemistry 34, 11–18, 2010
J.
Srividhya,
E.J. Crampin, P.E. McSharry, S. Schnell
Reconstructing
biochemical pathways from time course data
Proteomics 7,
828-838, 2007
J. Wildenhain,
E.J. Crampin
Reconstructing
gene regulatory networks: from random to scale-free connectivity
IEE Proc. Systems Biology 153
(4), 247-256, 2006
E.J. Crampin,
P.E. McSharry, S. Schnell
Extracting
biochemical reaction kinetics from time series data
Lecture Notes in A.I. 3214,
329-336, 2004
E.J. Crampin, S.
Schnell, P.E. McSharry
Mathematical
and computational techniques to deduce complex biochemical reaction
mechanisms
Progress in Biophysics & Molecular Biology
86 (1),
77-112, 2004
Collaborations:
Cris Print group
(Auckland), Mik Black (Otago), Santiago Schnell (University of
Michigan)
Recent Funding:
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