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The Therapeutic Landscape for KRAS-Mutated Colorectal Cancers
by
Whitehall, Vicki L. J.
, Burge, Matthew E.
, Tria, Simon Manuel
in
Apoptosis
/ Cancer therapies
/ Cell division
/ Colorectal cancer
/ Colorectal carcinoma
/ Immunotherapy
/ K-Ras protein
/ Kinases
/ Medical prognosis
/ Metabolic pathways
/ Metastases
/ Metastasis
/ Mutants
/ Mutation
/ Non-small cell lung carcinoma
/ Patients
/ Proteins
/ Review
/ Small cell lung carcinoma
2023
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The Therapeutic Landscape for KRAS-Mutated Colorectal Cancers
by
Whitehall, Vicki L. J.
, Burge, Matthew E.
, Tria, Simon Manuel
in
Apoptosis
/ Cancer therapies
/ Cell division
/ Colorectal cancer
/ Colorectal carcinoma
/ Immunotherapy
/ K-Ras protein
/ Kinases
/ Medical prognosis
/ Metabolic pathways
/ Metastases
/ Metastasis
/ Mutants
/ Mutation
/ Non-small cell lung carcinoma
/ Patients
/ Proteins
/ Review
/ Small cell lung carcinoma
2023
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Do you wish to request the book?
The Therapeutic Landscape for KRAS-Mutated Colorectal Cancers
by
Whitehall, Vicki L. J.
, Burge, Matthew E.
, Tria, Simon Manuel
in
Apoptosis
/ Cancer therapies
/ Cell division
/ Colorectal cancer
/ Colorectal carcinoma
/ Immunotherapy
/ K-Ras protein
/ Kinases
/ Medical prognosis
/ Metabolic pathways
/ Metastases
/ Metastasis
/ Mutants
/ Mutation
/ Non-small cell lung carcinoma
/ Patients
/ Proteins
/ Review
/ Small cell lung carcinoma
2023
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The Therapeutic Landscape for KRAS-Mutated Colorectal Cancers
Journal Article
The Therapeutic Landscape for KRAS-Mutated Colorectal Cancers
2023
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Overview
Colorectal cancer is one of the world’s most prevalent and lethal cancers. Mutations of the KRAS gene occur in ~40% of metastatic colorectal cancers. While this cohort has historically been difficult to manage, the last few years have shown exponential growth in the development of selective inhibitors targeting KRAS mutations. Their foremost mechanism of action utilizes the Switch II binding pocket and Cys12 residue of GDP-bound KRAS proteins in G12C mutants, confining them to their inactive state. Sotorasib and Adagrasib, both FDA-approved for the treatment of non-small cell lung cancer (NSCLC), have been pivotal in paving the way for KRAS G12C inhibitors in the clinical setting. Other KRAS inhibitors in development include a multi-targeting KRAS-mutant drug and a G12D mutant drug. Treatment resistance remains an issue with combination treatment regimens including indirect pathway inhibition and immunotherapy providing possible ways to combat this. While KRAS-mutant selective therapy has come a long way, more work is required to make this an effective and viable option for patients with colorectal cancer.
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