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

10 August 2010

Latest News

MTCI Investigator awarded €6 million funding by the EU to investigate possible treatments for difficult-to-treat types of Breast Cancer.
 

MTCI investigator successful in EU funded research project to investigate toxicity mechanisms of approved anti-angiogenesis cancer drugs

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Publications

Recent Publications

Duffy MJ, O'Donovan N, Corwn J. Use of molecular markers for predicting 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
 
O'Donovan N, Byrne AT, O'Connor AE, McGee S, Gallagher WM, Crown J. Synergistic interaction between trastuzumab and EGFR/HER-2 tyrosine kinase inhibitors in HER-2 positive breast cancer cells. Invest New Drugs. 2010; In Press. PMID: 20229355
 
Friel AM, Crown J, O’Driscoll L. Analysis of gene expression as relevant to cancer cells and circulating tumour cells. Meth. Mol. Biol. 2010; Book chapter. In press.
 
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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