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Molecular Biomarkers & Targets an overview Michael Messenger NIHR Diagnostic Evidence Co-Operative & Leeds Cancer Research UK Centre.

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Presentation on theme: "Molecular Biomarkers & Targets an overview Michael Messenger NIHR Diagnostic Evidence Co-Operative & Leeds Cancer Research UK Centre."— Presentation transcript:

1 Molecular Biomarkers & Targets an overview Michael Messenger NIHR Diagnostic Evidence Co-Operative & Leeds Cancer Research UK Centre

2 What is a biomarker? “a characteristic that is objectively measured and evaluated as an indicator of pathogenic processes, or responses to a therapeutic intervention.” (adapted from National Institute for Health, USA) Molecular Biomarkers include: – nucleic acids, proteins, lipids, polysaccharides and metabolites. Cancer Biomarkers: – associated with “The Hallmarks of Cancer”

3 Hallmarks of Cancer Sustaining proliferative signalling Evading growth suppressors Avoiding immune destruction Enabling replicative immortality Tumour – promoting inflammation Activating invasion & metastasis Inducing angiogenesis Genome instability & mutation Resisting cell death Deregulating cellular energetics Hanahan and Weinberg “Hallmarks of Cancer: The next generation” Cell 2001

4 How are biomarkers used clinically?

5 Molecular Targets (cancer) “an accessible molecular biomarker involved in a key biological process” the ideal target should have the following characteristics: –expressed only on/in tumour cells & not expressed on critical host/normal cells (Specific) –expressed on all tumour cells (Sensitive) –expressed in high numbers –no mutant or variant forms should be present –critical to cell survival –not shed, lost or circulated.

6 Molecular Targets (cancer)

7 Clinical Need in Colorectal Cancer Ability to detect and stage cancers intra- operatively Tumour-specific delivery of cytotoxic drugs or contrast agents for enhanced imaging Contact: Prof David Jayne D.G.Jayne@leeds.ac.uk

8 Potential targets in Colorectal Cancer

9 Clinical Need in Neuro-Oncology Glioblastoma multiforme (GBM) is the major unmet need in adult practice Tumour heterogeneity is a major challenge in defining useful targeted agents Targeting early events in gliomagenesis and common resistance mechanisms is appealing Contact: Prof Susan Short and Dr Heiko Wurdak S.C.Short@leeds.ac.uk H.Wurdak@leeds.ac.uk

10 Potential targets in Neuro-Oncology Targeting Stem cell phenotype: SOX2 has emerged as major driver in GBM stem cell population SOX2 inactivator Targeting early events in gliomagenesis: IDH1mutation is initiating mutation in secondary GBM Cytotoxic specific to IDHmut cells Targeting common resistance mechanisms: MGMT repair enzyme expression limits effectiveness of chemotherapy in 60% of cases MGMT inhibitor Contact: Prof Susan Short and Dr Heiko Wurdak S.C.Short@leeds.ac.uk H.Wurdak@leeds.ac.uk

11 Clinical Need in Urological Cancers Renal Cancer – No biomarkers in routine clinical use, tools for better diagnosis and prognosis required – Resistant to chemotherapy. Few treatment options Bladder Cancer – No biomarkers in routine use – Treatments have not changed for >20 years. Contact: Dr Naveen Vasudev N.Vasudev@leeds.ac.uk

12 Potential Targets in Urological Cancers Harnessing the immune system – PD1 / PDL-1 antibodies - Promising activity in kidney and bladder cancer Powles et al. Nature 2014 Complete remission in a patient with metastatic bladder cancer Renal cancer imaging – CAIX labelled antibodies - eg Superparamagnetic iron oxide (SPIO) nanoparticles and mAb G250 conjugated as mMRI probe Lu et al. Plos One 2014 Contact: Dr Naveen Vasudev N.Vasudev@leeds.ac.uk

13 Clinical Need in Breast cancer Tamoxifen- the first targeted cancer therapy Need for precision medicine to match patients to therapies Deliver drugs more specifically and reduce toxicity General need for targeting – MicroRNAs – Tumour stroma Fibroblasts Immune infiltrates Contact: Prof Val Spears and Peter Hall V.Speirs@leeds.ac.uk p.s.hall@leeds.ac.uk

14 Potential Targets in Breast cancer Specific gene targets – FGFR2 consistently identified as a breast cancer risk locus – CDK4/6 – PI3K/AKT/mTOR – PARP – Src – HDAC All identified from pre-clinical studies examining the mechanisms driving resistance Contact: Prof Val Spears V.Speirs@leeds.ac.uk

15 Next Generation Target Discovery

16 Acknowledgements Peter Selby David Jayne Susan Short Heiko Wurdak Naveen Vasudev Val Spears

17 Example: Herceptin


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