Gene interactions and pathways from curated databases and text-mining

◀ Back to HRAS

HRAS — KRAS

Pathways - manually collected, often from reviews:

Protein-Protein interactions - manually collected from original source literature:

Studies that report less than 10 interactions are marked with *

Text-mined interactions from Literome

Cengel et al., Cancer Biol Ther 2006 (Pancreatic Neoplasms) : Thus, radiosensitization of human cancer cells that express mutated K-RAS occurred under conditions where AZD3409 inihibits the activation of farneyslated H-RAS , but did not inhibit K-RAS activation
Cengel et al., Neoplasia (New York, N.Y.) 2007 (Colorectal Neoplasms...) : Taken together, these findings suggest that EGFR activated H-Ras signaling is initiated by oncogenic K-Ras to promote radiation survival in pancreatic and colorectal cancers
Li et al., Zhongguo Yi Xue Ke Xue Yuan Xue Bao 1990 (Carcinoma, Hepatocellular...) : However, the mRNA expression of c-Ha-ras , c-N-Ras and c-myc oncogenes was enhanced by 4 mmol/L sodium butyrate treatment, while the expression of c-Ki-ras and c-fos remained unchanged
Li et al., Blood 2011 (Leukemia, Myeloid, Acute...) : We found that endogenous Kras ( G12D ) expression results in markedly elevated Ras protein expression and Ras-GTP levels in Mac1 ( + ) cells, whereas Mx1-Cre, LSL-Nras ( G12D ) mice show much lower Ras protein and Ras-GTP levels
Wang et al., FASEB J 2011 : Dominant negative H-Ras or K-Ras reduced accumulation of H-Ras and K-Ras in focal adhesions induced by IL-1 and also blocked ERK activation and focal adhesion maturation
Quincoces et al., FEBS Lett 1997 : In quiescent NIH3T3 cells transfected with inducible H-ras oncogenes, the induction of H-Ras was followed 12 h later by a 3-fold increase in the mRNA expression of endogenous K-ras and N-ras
Stayrook et al., Anticancer Res 1998 (Pancreatic Neoplasms) : Interestingly, H-Ras , but not K-Ras, farnesylation was inhibited by perillyl alcohol, and perillyl alcohol inhibited MAP kinase phosphorylation in H-ras but not K-ras oncogene transformed pancreatic cells