IL13Rα2-targeted therapy for pancreatic cancer

  • Research type

    Research Study

  • Full title

    Investigation of IL13Rα2-targeted therapy for pancreatic cancer

  • IRAS ID

    220376

  • Contact name

    Venkateswarlu Kanamarlapudi

  • Contact email

    k.venkateswarlu@swansea.ac.uk

  • Sponsor organisation

    Swansea University

  • Duration of Study in the UK

    2 years, 11 months, 31 days

  • Research summary

    Pancreatic cancer has a very poor survival rate with currently only 5% of newly-diagnosed patients surviving for more than 5 years. This extremely poor outlook is in part due to the fact that pancreatic tumours are highly resistant to standard cancer drug treatments. Therefore, new treatment options are urgently required for this type of cancer. In this regard, we and others have shown that the interleukin-13 receptor alpha 2 (IL-13Rα2) protein is over-expressed on the surface of pancreatic cancer cells, highlighting the possibility that this molecule may represent a novel drug target. Towards this end, we have developed a small peptide-based drug (Pep1-Phor21) that specifically binds to IL-13Rα2 on the surface of tumour cells and selectively kills them. Unlike many standard chemotherapies which operate inside cells, this new drug should be more effective as it rapidly kills cancer cells by working outside at the cell surface, circumventing many of the drug-resistance problems associated with established chemotherapies. To date, we have extensively investigated the specific activity of the experimental drug on cultured pancreatic tumour cell lines and to gain further insight as to how this drug will perform in patients, it is now essential that we further investigate the expression of the drug target and define the activity of this new drug on primary tumour samples from patients.

  • REC name

    East Midlands - Nottingham 1 Research Ethics Committee

  • REC reference

    17/EM/0071

  • Date of REC Opinion

    15 Feb 2017

  • REC opinion

    Favourable Opinion