Increased signalling by the small G protein Ras is found in many human cancers and is often caused by direct mutation of this protein. Hence, small-molecule attenuation of pathological Ras activity is of utmost interest in oncology. However, despite nearly three decades of intense drug discovery efforts, no clinically viable option for Ras inhibition has been developed. Very recently, reports of a number of new approaches of addressing Ras activity have led to the revival of this molecular target with the prospect of finally fulfilling the therapy promises associated with this important protein
RAS drug development has made enormous strides in the past ten years, with the first direct KRAS inh...
Around 20% of all malignancies harbour activating mutations in RAS isoforms. Despite this, there is ...
2noThe Ras pathway is frequently deregulated in cancer, actively contributing to tumor development a...
Increased signalling by the small G protein Ras is found in many human cancers and is often caused b...
Ras proteins are key elements in the regulation of cellular proliferation, differentiation and survi...
Abnormal expression or mutations in Ras proteins has been found in up to 30 % of cancer cell types, ...
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common oncogenes, and around 19% of...
RAS mutations are the most common gain-of-function change in human cancer and promise to be a critic...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
K-Ras proteins are major drivers of human cancers, playing a direct causal role in about one million...
Despite more than three decades of intensive effort, no effective pharmacologic inhibitors of the Ra...
AbstractThree decades after identification of the Ras oncogene, no effective treatments for Ras muta...
RAS oncogenes are the most commonly mutated oncogenes in human cancer, and RAS-mutant cancers repres...
Around 20% of all malignancies harbour activating mutations in RAS isoforms. Despite this, there is ...
KRAS is the most frequently activated oncogene in human cancer, but it has, so far, shrugged off all...
RAS drug development has made enormous strides in the past ten years, with the first direct KRAS inh...
Around 20% of all malignancies harbour activating mutations in RAS isoforms. Despite this, there is ...
2noThe Ras pathway is frequently deregulated in cancer, actively contributing to tumor development a...
Increased signalling by the small G protein Ras is found in many human cancers and is often caused b...
Ras proteins are key elements in the regulation of cellular proliferation, differentiation and survi...
Abnormal expression or mutations in Ras proteins has been found in up to 30 % of cancer cell types, ...
Abstract RAS mutations (HRAS, NRAS, and KRAS) are among the most common oncogenes, and around 19% of...
RAS mutations are the most common gain-of-function change in human cancer and promise to be a critic...
Mutations of RAS oncogenes are responsible for about 30% of all human cancer types, including pancre...
K-Ras proteins are major drivers of human cancers, playing a direct causal role in about one million...
Despite more than three decades of intensive effort, no effective pharmacologic inhibitors of the Ra...
AbstractThree decades after identification of the Ras oncogene, no effective treatments for Ras muta...
RAS oncogenes are the most commonly mutated oncogenes in human cancer, and RAS-mutant cancers repres...
Around 20% of all malignancies harbour activating mutations in RAS isoforms. Despite this, there is ...
KRAS is the most frequently activated oncogene in human cancer, but it has, so far, shrugged off all...
RAS drug development has made enormous strides in the past ten years, with the first direct KRAS inh...
Around 20% of all malignancies harbour activating mutations in RAS isoforms. Despite this, there is ...
2noThe Ras pathway is frequently deregulated in cancer, actively contributing to tumor development a...