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The RAS proto-oncogene family (HRAS, KRAS, NRAS) encodes small GTPases that function as molecular switches in signaling pathways regulating cell proliferation, differentiation, and survival. Mutations in RAS genes, particularly KRAS, are highly prevalent in various cancers, leading to constitutive activation of downstream signaling and uncontrolled cell growth. Targeting mutant RAS, especially KRAS G12C, has emerged as a promising therapeutic strategy.
Inhibition of RAS GTPase activity, irreversible modification of cysteine at position 12 (e.g., KRAS G12C inhibitors)
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