Dissecting mechanisms of resistance to targeted drug combination therapy in human colorectal cancer

• Published in: Oncogene 2019-06, Vol.38 (25), p.5076-5090
• Main Authors: Clarke, Paul A., Roe, Toby, Swabey, Kate, Hobbs, Steve M., McAndrew, Craig, Tomlin, Kathy, Westwood, Isaac, Burke, Rosemary, van Montfort, Robert, Workman, Paul
• Format: Article
• Language: English
• Subjects: 1-Phosphatidylinositol 3-kinase; 13/106; 42/89; 631/337; 631/67/1504/1885; 631/80/86; 82/80; 96/95; Aniline Compounds - administration & dosage; Antineoplastic Combined Chemotherapy Protocols - therapeutic use; Apoptosis; Cancer; Cancer therapies; Cell Biology; Cellular signal transduction; Colorectal cancer; Colorectal carcinoma; Colorectal Neoplasms - drug therapy; Colorectal Neoplasms - genetics; Colorectal Neoplasms - metabolism; Colorectal Neoplasms - pathology; Drug resistance; Drug Resistance, Neoplasm - genetics; Drug therapy; Drug therapy, Combination; Genetic aspects; Genotypes; HCT116 Cells; Human Genetics; Humans; Internal Medicine; MAP kinase; MAP Kinase Kinase 1 - antagonists & inhibitors; MAP Kinase Kinase 1 - genetics; MAP Kinase Kinase 1 - metabolism; MAP Kinase Kinase 2 - antagonists & inhibitors; MAP Kinase Kinase 2 - genetics; MAP Kinase Kinase 2 - metabolism; MAP Kinase Signaling System - drug effects; Medicine; Medicine & Public Health; MEK inhibitors; Molecular Targeted Therapy - methods; Mutation; Oncology; Protein Kinase Inhibitors - administration & dosage; Proto-Oncogene Proteins c-bcl-2 - antagonists & inhibitors; PTEN Phosphohydrolase - antagonists & inhibitors; PTEN Phosphohydrolase - genetics; PTEN Phosphohydrolase - metabolism; PTEN protein; Risk factors; Signal transduction; Signal Transduction - genetics; Sulfonamides - administration & dosage; Tumor cell lines; Tumor Cells, Cultured; Tumors
• ISSN: 0950-9232; 1476-5594
• DOI: 10.1038/s41388-019-0780-z

Genomic alterations in cancer cells result in vulnerabilities that clinicians can exploit using molecularly targeted drugs, guided by knowledge of the tumour genotype. However, the selective activity of these drugs exerts an evolutionary pressure on cancers that can result in the outgrowth of resistant clones. Use of rational drug combinations can overcome resistance to targeted drugs, but resistance may eventually develop to combinatorial therapies. We selected MAPK- and PI3K-pathway inhibition in colorectal cancer as a model system to dissect out mechanisms of resistance. We focused on these signalling pathways because they are frequently activated in colorectal tumours, have well-characterised mutations and are clinically relevant. By treating a panel of 47 human colorectal cancer cell lines with a combination of MEK- and PI3K-inhibitors, we observe a synergistic inhibition of growth in almost all cell lines. Cells with KRAS mutations are less sensitive to PI3K inhibition, but are particularly sensitive to the combined treatment. Colorectal cancer cell lines with inherent or acquired resistance to monotherapy do not show a synergistic response to the combination treatment. Cells that acquire resistance to an MEK–PI3K inhibitor combination treatment still respond to an ERK–PI3K inhibitor regimen, but subsequently also acquire resistance to this combination treatment. Importantly, the mechanisms of resistance to MEK and PI3K inhibitors observed, MEK1/2 mutation or loss of PTEN, are similar to those detected in the clinic. ERK inhibitors may have clinical utility in overcoming resistance to MEK inhibitor regimes; however, we find a recurrent active site mutation of ERK2 that drives resistance to ERK inhibitors in mono- or combined regimens, suggesting that resistance will remain a hurdle. Importantly, we find that the addition of low concentrations of the BCL2-family inhibitor navitoclax to the MEK–PI3K inhibitor regimen improves the synergistic interaction and blocks the acquisition of resistance.