Targeting KRAS in Cancer: Promising Therapeutic Strategies
- PMID: 33801965
- PMCID: PMC7999304
- DOI: 10.3390/cancers13061204
Targeting KRAS in Cancer: Promising Therapeutic Strategies
Abstract
The Kirsten rat sarcoma viral oncogene homolog (KRAS) is mutated in approximately 25% of all human cancers and is known to be a major player promoting and maintaining tumorigenesis through the RAS/MAPK pathway. Over the years, a large number of studies have identified strategies at different regulatory levels to tackle this 'difficult-to-target' oncoprotein. Yet, the most ideal strategy to overcome KRAS and its downstream effects has yet to be uncovered. This review summarizes the role of KRAS activating mutations in multiple cancer types as well as the key findings for potential strategies inhibiting its oncogenic behavior. A comprehensive analysis of the different pathways and mechanisms associated with KRAS activity in tumors will ultimately pave the way for promising future work that will identify optimum therapeutic strategies.
Keywords: EGFR; KRAS; MAPK; cancer; mutations; targeted-therapy.
Conflict of interest statement
The authors declare no conflict of interest.
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