The Repurposing of Non-Peptide Neurokinin-1 Receptor Antagonists as Antitumor Drugs: An Urgent Challenge for Aprepitant.
Rafael CoveñasFrancisco David RodriguezPrema RobinsonMiguel MuñozPublished in: International journal of molecular sciences (2023)
The substance P (SP)/neurokinin-1 receptor (NK-1R) system is involved in cancer progression. NK-1R, activated by SP, promotes tumor cell proliferation and migration, angiogenesis, the Warburg effect, and the prevention of apoptosis. Tumor cells overexpress NK-1R, which influences their viability. A typical specific anticancer strategy using NK-1R antagonists, irrespective of the tumor type, is possible because these antagonists block all the effects mentioned above mediated by SP on cancer cells. This review will update the information regarding using NK-1R antagonists, particularly Aprepitant, as an anticancer drug. Aprepitant shows a broad-spectrum anticancer effect against many tumor types. Aprepitant alone or in combination therapy with radiotherapy or chemotherapy could reduce the sequelae and increase the cure rate and quality of life of patients with cancer. Current data open the door to new cancer research aimed at antitumor therapeutic strategies using Aprepitant. To achieve this goal, reprofiling the antiemetic Aprepitant as an anticancer drug is urgently needed.
Keyphrases
- chemotherapy induced
- nk cells
- combination therapy
- papillary thyroid
- oxidative stress
- squamous cell
- emergency department
- endoplasmic reticulum stress
- stem cells
- cell death
- single cell
- squamous cell carcinoma
- healthcare
- vascular endothelial growth factor
- minimally invasive
- big data
- young adults
- artificial intelligence
- radiation induced
- data analysis
- binding protein