ABI Systems Biology Group: Research


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:


 
       

 Auckland Bioengineering Institute / Systems Biology Group / Research Projects