One of the most frequently mutated oncogenes in human cancer, KRAS has long been considered “undruggable” with targeted therapy. As central drivers of cancer progressions, KRAS mutations function as oncogenic initiators, instigating the proliferation of malignant cells. The result is the rapid expansion of resistant malignant tissue.
Targeting these mutations is imperative to advancing cancer therapy, and in light of recent developments in the field, BMC Cancer has published this Collection on Cancer therapy: KRAS targeted therapies.
We encouraged submissions on a range of topics, including but not limited to:
- Novel strategies, such as small molecule inhibitors, immunotherapies, and gene-based therapies, designed specifically for addressing KRAS-mutated cancers
- Studies that assess the safety, effectiveness, and tolerability of KRAS targeted therapies across cancer types
- Precise biomarkers and diagnostic tools
- Potential synergistic effects arising from combining KRAS targeted agents with conventional cancer treatments
- Mechanisms responsible for resistance to KRAS targeted therapies
- Analyses of real-world clinical results
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