A Science Foundation Ireland founded Strategic Research Cluster in association with DCU, UCD, TCD, RCSI and ICORG

Welcome to Molecular Therapeutics for Cancer Ireland

Molecular Therapeutics for Cancer, Ireland (MTCI) is a Science Foundation Ireland-funded Strategic Research Cluster which aims to discover and develop new anti-cancer drugs.

There is an urgent need for improved drug treatments for cancer, which is emerging as the leading cause of mortality in Ireland and other western countries. Traditional cancer chemotherapy has resulted in improved outcomes for some types of cancer, but remains a generally unsatisfactory form of treatment, with low rates of cure, and prominent side-effects.

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The developmental process for many of these older drugs was based on a form of trial and error, i.e. candidate chemicals were administered to cancer cells to see if they stopped them from growing. If they did, they were taken to further levels of testing and ultimately given to patients with cancer. As such it is not surprising that activity was often marginal, and toxicity was common.

There is now a much greater understanding of the molecular basis of malignancy, and multiple potential molecular targets for new drugs have been identified. The introduction of novel rationally designed molecularly targeted treatments has revolutionised the treatment of some types of cancer. The best example is imatinib, an agent which has resulted in a dramatically improved outcome for patients with chronic myeloid leukaemia, and with gastro-intestinal stromal tumours. Another drug, trastuzumab (better known as herceptin) has resulted in substantially improved outcome for patients with one of the most aggressive forms of breast cancer. Molecular treatments have also improved the outcome for patients with other tumours including cancers of the colon, kidney, lung and lymph system.

The developmental process for these new anticancer drugs has undergone radical change in the molecular era. Unlike the empirical approach used to discover chemotherapy drugs, the new approach is mechanistic and molecular.

Another critical difference is that the new approach is “translational”, i.e. it involves intense interaction between laboratory and clinical investigators. Thus, modern cancer drug development begins with recognition of clinical need, and progresses through molecular target identification, drug synthesis, pre-clinical testing, clinical trials and molecular analysis of tissue samples from treated patients

Many critical components of the development process for molecular cancer therapeutics exist in Ireland, but are dispersed across multiple institutions. Molecular Therapeutics for Cancer Ireland represents an attempt to capitalise on potential synergies between these resources, in order to develop “Ireland Inc.” as a site for cancer drug development.

News

01 February 2012

MTCI

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Publications

Recent Publications

Brennan DJ, O’Connor DP, Rexhepaj E, Ponten F, Gallagher WM. Antibody-based proteomics: fast-tracking molecular diagnostics in oncology. Nat Rev Cancer 2010; 10(9):605-17. PMID: 20720569

Corcoran C, Friel AM, Duffy MJ, Crown J, O’Driscoll L. Invited review: Intracellular and extracellular microRNAs in breast cancer. Clin Chem. 2011. In press. PMID: 21059829

Madden SF, Carpenter SB, Jeffery IB, Bjorkbacka H, Fitzgerald KA, O’Neill LA, Higgins DG. Detecting microRNA activity from gene expression data. BMC Bioinformatics. 2010 18(11):257. PMID: 20482775

Duffy MJ, O’Donovan N, Crown J. Use of molecular markers for predicting therapy response in cancer patients. Cancer Treat Rev. 2010; In press. PMID: 2068042

Browne BC, Crown J, Venkatesan N, Duffy MJ, Clynes M, Slamon D, O’Donovan N. Inhibition of IGF1R activity enhances response to trastuzumab in HER-2 positive breast cancer cells. Ann Oncol. 2010; In press. PMID: 20647220

Friel AM, Corcoran C, Crown J, O’Driscoll L. Relevance of circulating tumour cells, extracellular nucleic acids and exosomes in breast cancer. Breast Cancer Res Treat. 2010 123(3):613-25. PMID: 20549336

O’Neill K, Lyons SK, Gallagher WM, Curran KM, Byrne AT. Review Article. Bioluminescent imaging: a critical tool in pre-clinical oncology research. J Pathol. 2010; 220 (3): 317-327. PMID: 19967724.

O'Brien NA, Browne BC, Chow L, Wang Y, Ginther C, Arboleda J, Duffy MJ, Crown J, O'Donovan N, Slamon DJ. Activated Phosphoinositide 3-Kinase/AKT signaling confers resistance to trastuzumab but not lapatinib. Mol Can Ther 2010; 9(6):1489-502. PMID: 20501798

 

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