KRAS: From undruggable to a druggable Cancer Target
D Uprety, AA Adjei - Cancer treatment reviews, 2020 - Elsevier
RAS is the most frequently mutated oncogene in human cancers, with mutations in about
30% of all cancers. RAS exists in three different isoforms (K-RAS, H-RAS and N-RAS) with …
30% of all cancers. RAS exists in three different isoforms (K-RAS, H-RAS and N-RAS) with …
Role of artificial intelligence in radiogenomics for cancers in the era of precision medicine
Simple Summary Recently, radiogenomics has played a significant role and offered a new
understanding of cancer's biology and behavior in response to standard therapy. It also …
understanding of cancer's biology and behavior in response to standard therapy. It also …
Comutations and KRASG12C Inhibitor Efficacy in Advanced NSCLC
MV Negrao, HA Araujo, G Lamberti, AJ Cooper… - Cancer discovery, 2023 - AACR
Molecular modifiers of KRASG12C inhibitor (KRASG12Ci) efficacy in advanced KRAS G12C-
mutant NSCLC are poorly defined. In a large unbiased clinicogenomic analysis of 424 …
mutant NSCLC are poorly defined. In a large unbiased clinicogenomic analysis of 424 …
KRAS oncogene in non-small cell lung cancer: clinical perspectives on the treatment of an old target
Lung neoplasms are the leading cause of death by cancer worldwide. Non-small cell lung
cancer (NSCLC) constitutes more than 80% of all lung malignancies and the majority of …
cancer (NSCLC) constitutes more than 80% of all lung malignancies and the majority of …
Idiopathic pulmonary fibrosis and lung cancer: mechanisms and molecular targets
B Ballester, J Milara, J Cortijo - International journal of molecular sciences, 2019 - mdpi.com
Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pulmonary
disease with a median survival of 2–4 years after diagnosis. A significant number of IPF …
disease with a median survival of 2–4 years after diagnosis. A significant number of IPF …
Biochemical and structural analysis of common cancer-associated KRAS mutations
JC Hunter, A Manandhar, MA Carrasco, D Gurbani… - Molecular cancer …, 2015 - AACR
KRAS mutations are the most common genetic abnormalities in cancer, but the distribution
of specific mutations across cancers and the differential responses of patients with specific …
of specific mutations across cancers and the differential responses of patients with specific …
[HTML][HTML] K-ras mutation subtypes in NSCLC and associated co-occuring mutations in other oncogenic pathways
M Scheffler, MA Ihle, R Hein… - Journal of Thoracic …, 2019 - Elsevier
Introduction Although KRAS mutations in NSCLC have been considered mutually exclusive
driver mutations for a long time, there is now growing evidence that KRAS-mutated NSCLC …
driver mutations for a long time, there is now growing evidence that KRAS-mutated NSCLC …
The state of the art for artificial intelligence in lung digital pathology
Lung diseases carry a significant burden of morbidity and mortality worldwide. The advent of
digital pathology (DP) and an increase in computational power have led to the development …
digital pathology (DP) and an increase in computational power have led to the development …
[HTML][HTML] Mutation patterns in a population-based non-small cell lung cancer cohort and prognostic impact of concomitant mutations in KRAS and TP53 or STK11
L La Fleur, E Falk-Sörqvist, P Smeds, A Berglund… - Lung cancer, 2019 - Elsevier
Objectives Non-small cell lung cancer (NSCLC) is a heterogeneous disease with unique
combinations of somatic molecular alterations in individual patients, as well as significant …
combinations of somatic molecular alterations in individual patients, as well as significant …
Direct Targeting KRAS Mutation in Non-Small Cell Lung Cancer: Focus on Resistance
D Reita, L Pabst, E Pencreach, E Guérin, L Dano… - Cancers, 2022 - mdpi.com
Simple Summary KRAS is the most frequently mutated oncogene in non-small cell lung
cancers (NSCLC), with a frequency around 30%, and among them KRAS G12C mutation …
cancers (NSCLC), with a frequency around 30%, and among them KRAS G12C mutation …