Harnessing the ion transportome to treat cancer
Abstract Despite significant advances in early detection and therapeutic opportunities, cancer remains a critical global health challenge. The greatest barrier to reducing cancer‐associated mortality is the persistent problem of therapeutic resistance and metastasis. Standard treatment approaches, including surgery combined with chemotherapy and radiation, are effective for many patients with localised disease. However, a substantial proportion of patients will experience recurrence and therapy resistance, leading to treatment failure and poor outcomes. This adverse prognosis for patients highlights the critical need to identify new therapeutic targets capable of improving long‐term survival. The ion transportome comprises ion channels, solute transporters and pumps that regulate controlled movement of sodium (Na + ), potassium (K + ), calcium (Ca 2+ ), chloride (Cl − ) and hydrogen (H + ) across cell membranes. Ion transport is central to many cellular processes, including cell growth, volume regulation, proliferation and migration. In many solid tumours, the finely tuned ionic balance becomes dysregulated, with aberrant expression or activity of membrane transport proteins being closely linked to many of the hallmarks of cancer. Ion channel modulation using pharmacological agents designed to treat channelopathies has demonstrated promise in suppressing cancer progression in preclinical models. Thus, targeting ion‐driven vulnerabilities within solid tumours may complement existing therapies to overcome resistance and improve patient outcomes. The dynamic nature of ion transport mechanisms means that addressing critical research questions regarding their suitability as pharmacological targets is challenging, highlighting the need to develop innovative approaches to study these processes in oncology. image
Authors
- A. James
- Ruth D. Murrell‐Lagnado (ORCID: https://orcid.org/0000-0003-2743-7977)
- Sara Moodad (ORCID: https://orcid.org/0000-0001-8332-6601)
- Şerife Yerlikaya (ORCID: https://orcid.org/0000-0002-5349-7298)
- Jason Bruce
- Alina Capatina
- Amanda Foust
- Thomas; id_orcid 0000-0003-1768-3808 Eykyn
- Orkun Soyer
- Antony Jackson
- Robinson, Hugh, 1584?-1655
- Karen McCloskey
- Samantha Salvage
- Elizabeth Fitzgerald
- Jodie Malcolm
- Sarah Lilley
- Paul Buchanan
- Alson Huang
- Frederick Jones
- Jonathan Ashmore
- Aamir Ahmed
- Stuart Higgins
- WILLIAM BRACKENBURY
- Yoshikatsu Hayashi
- Tim G. Hales (ORCID: https://orcid.org/0000-0002-2040-9714)
Institutions
- Manchester Metropolitan University (GB)
- Queen's University Belfast (GB)
- East Sussex County Council (GB)
- University of Sussex (GB)
- St George's, University of London (GB)
- University of Dundee (GB)
- King's College London (GB)
- University of Cambridge (GB)
- Yorkshire Cancer Research (GB)
- University of Manchester (GB)
- Istanbul Medipol University (TR)
- University of Warwick (GB)
- MRC Laboratory for Molecular Cell Biology (GB)
- Dublin City University (IE)
- University College London (GB)
- Imperial College London (GB)
- University of York (GB)
- University of Reading (GB)
Publication Details
- Journal
- The Journal of Physiology
- Published
- 2026-10-18
- DOI
- https://doi.org/10.1113/jp290738
- Primary Topic
- Ion Transport and Channel Regulation
- Type
- article
- Field-Weighted Citation Impact
- 0.00