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UCSC Genome Browser Gene Interaction Graph
Gene interactions and pathways from curated databases and text-mining

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EGFR — YBX1

Text-mined interactions from Literome

Wu et al., Cancer Res 2006 (Breast Neoplasms) : Disruption of the Y-box binding protein-1 results in suppression of the epidermal growth factor receptor and HER-2 ... It was inversely linked to the estrogen receptor ( P < 0.001, r = -0.291 ). Overexpression of YB-1 in a breast cancer cell line increased HER-2 and EGFR. Alternatively, mutation of YB-1 at Ser ( 102 ) > Ala ( 102 ) prevented the induction of these receptors and rendered the cells less responsive to EGF
To et al., Mol Pharmacol 2007 (Breast Neoplasms) : We reported that EGFR expression is induced by the oncogenic transcription factor Y-box binding protein-1 (YB-1) that occurs in a manner dependent on phosphorylation by Akt
Stratford et al., Breast Cancer Res 2007 (Breast Neoplasms) : Epidermal growth factor receptor (EGFR) is transcriptionally induced by the Y-box binding protein-1 (YB-1) and can be inhibited with Iressa in basal-like breast cancer, providing a potential target for therapy ... We pursued this in light of our recent work showing that YB-1 induces the expression of EGFR , a new BLBC marker ... We determined the regulatory role of Y-box binding protein-1 (YB-1) on epidermal growth factor receptor (EGFR) overexpression in BLBC, and the therapeutic potential of inhibiting EGFR
Kashihara et al., J Thorac Oncol 2009 (Carcinoma, Non-Small-Cell Lung...) : In the five NSCLC cell lines, expressions of EGFR , human epidermal growth factor receptor 2 ( HER2 ), HER3, and hepatocyte growth factor receptor ( c-Met ) in PC-9 cells ; of HER2 and c-Met in EBC-1 cells ; and of HER3 in QG56 cells were down-regulated by YB-1 knockdown
Xie et al., Tumour Biol 2012 (Breast Neoplasms) : The expression of YB-1 in the nucleus of breast cancer cells positively correlated with the Scarff-Bloom-Richardson grade ( P = 0.007 ) and HER-2 expression ( P = 0.005 ), negatively correlated with ER expression ( P = 0.004 ), and was independent of the age, menstrual status, pathological type, tumor size, lymph node status, presence of thrombosis, PR expression, and EGFR expression