Identifying Novel Actionable Targets in Colon Cancer.
Maria Grazia CerritoEmanuela GrassilliPublished in: Biomedicines (2021)
Colorectal cancer is the fourth cause of death from cancer worldwide, mainly due to the high incidence of drug-resistance toward classic chemotherapeutic and newly targeted drugs. In the last decade or so, the development of novel high-throughput approaches, both genome-wide and chemical, allowed the identification of novel actionable targets and the development of the relative specific inhibitors to be used either to re-sensitize drug-resistant tumors (in combination with chemotherapy) or to be synthetic lethal for tumors with specific oncogenic mutations. Finally, high-throughput screening using FDA-approved libraries of "known" drugs uncovered new therapeutic applications of drugs (used alone or in combination) that have been in the clinic for decades for treating non-cancerous diseases (re-positioning or re-purposing approach). Thus, several novel actionable targets have been identified and some of them are already being tested in clinical trials, indicating that high-throughput approaches, especially those involving drug re-positioning, may lead in a near future to significant improvement of the therapy for colon cancer patients, especially in the context of a personalized approach, i.e., in defined subgroups of patients whose tumors carry certain mutations.
Keyphrases
- high throughput
- drug resistant
- clinical trial
- genome wide
- multidrug resistant
- end stage renal disease
- acinetobacter baumannii
- newly diagnosed
- ejection fraction
- chronic kidney disease
- primary care
- dna methylation
- drug induced
- single cell
- peritoneal dialysis
- squamous cell carcinoma
- papillary thyroid
- risk factors
- transcription factor
- emergency department
- current status
- cancer therapy
- locally advanced
- pseudomonas aeruginosa
- radiation therapy
- drug delivery
- study protocol
- drug administration
- childhood cancer