がん進展制御研究所Mutations in Kirsten rat-sarcoma (KRAS) are well appreciated to be major drivers of human cancers through dysregulation of multiple growth and survival pathways. Similar to many other non-kinase oncogenes and tumor suppressors, efforts to directly target KRAS pharmaceutically have not yet materialized. As a result, there is broad interest in an alternative approach to develop therapies that induce synthetic lethality in cancers with mutant KRAS, therefore exposing the particular vulnerabilities of these cancers. Fueling these efforts is our increased understanding into the biology driving KRAS mutant cancers, in particular the important pathways that mutant KRAS governs to promote survival. In this mini-review, we summarize the lat...
: Non-small cell lung cancer (NSCLC) represents the perfect paradigm of 'precision medicine' due to ...
KRAS phosphorylation has been reported recently to modulate the activity of mutant KRAS protein in v...
Rationale: KRAS is the most common and, simultaneously, the most ambiguous oncogene implicated in hu...
Mutations in KRAS are among the most frequent aberrations in cancer, including colon cancer. KRAS di...
Mutations in Kristen Rat Sarcoma viral oncogene (KRAS) are among the most frequent gain-of-function ...
AbstractMutations in the KRAS oncogene represent one of the most prevalent genetic alterations in co...
The development of pharmacologic inhibitors of the KRAS oncoprotein, which is mutated in ~30% of all...
Current evidence strongly suggests that cancer cells depend on the microenvironment in order to thri...
Activating mutations in KRAS are present in 25% of human cancers. When mutated, the KRAS protein bec...
SummaryKRAS is the most frequently mutated oncogene in human cancer, yet no therapies are available ...
Despite having been identified over thirty years ago and definitively established as having a critic...
Approximately 15% of all cancer patients harbor mutated KRAS. Direct inhibitors of KRAS have now bee...
For decades, KRAS mutant lung adenocarcinomas (LUAD) have been refractory to therapeutic strategies ...
KRAS mutations occur in a quarter of all of human cancers, yet no selective drug has been approved t...
Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health and Science...
: Non-small cell lung cancer (NSCLC) represents the perfect paradigm of 'precision medicine' due to ...
KRAS phosphorylation has been reported recently to modulate the activity of mutant KRAS protein in v...
Rationale: KRAS is the most common and, simultaneously, the most ambiguous oncogene implicated in hu...
Mutations in KRAS are among the most frequent aberrations in cancer, including colon cancer. KRAS di...
Mutations in Kristen Rat Sarcoma viral oncogene (KRAS) are among the most frequent gain-of-function ...
AbstractMutations in the KRAS oncogene represent one of the most prevalent genetic alterations in co...
The development of pharmacologic inhibitors of the KRAS oncoprotein, which is mutated in ~30% of all...
Current evidence strongly suggests that cancer cells depend on the microenvironment in order to thri...
Activating mutations in KRAS are present in 25% of human cancers. When mutated, the KRAS protein bec...
SummaryKRAS is the most frequently mutated oncogene in human cancer, yet no therapies are available ...
Despite having been identified over thirty years ago and definitively established as having a critic...
Approximately 15% of all cancer patients harbor mutated KRAS. Direct inhibitors of KRAS have now bee...
For decades, KRAS mutant lung adenocarcinomas (LUAD) have been refractory to therapeutic strategies ...
KRAS mutations occur in a quarter of all of human cancers, yet no selective drug has been approved t...
Cancer Early Detection Advanced Research (CEDAR), Knight Cancer Institute, Oregon Health and Science...
: Non-small cell lung cancer (NSCLC) represents the perfect paradigm of 'precision medicine' due to ...
KRAS phosphorylation has been reported recently to modulate the activity of mutant KRAS protein in v...
Rationale: KRAS is the most common and, simultaneously, the most ambiguous oncogene implicated in hu...