Title : Drugs that target specificity proteins downregulate epidermal growth factor receptor in bladder cancer cells.

Pub. Date : 2010 May

PMID : 20407012






6 Functional Relationships(s)
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1 BA, curcumin, and iSp also decreased phosphorylation of Akt in these cells, and downregulation of EGFR by BA, curcumin, and iSp was accompanied by induction of LC3 and autophagy, which is consistent with recent studies showing that EGFR suppresses autophagic cell death. Curcumin epidermal growth factor receptor Homo sapiens
2 BA, curcumin, and iSp also decreased phosphorylation of Akt in these cells, and downregulation of EGFR by BA, curcumin, and iSp was accompanied by induction of LC3 and autophagy, which is consistent with recent studies showing that EGFR suppresses autophagic cell death. Curcumin epidermal growth factor receptor Homo sapiens
3 BA, curcumin, and iSp also decreased phosphorylation of Akt in these cells, and downregulation of EGFR by BA, curcumin, and iSp was accompanied by induction of LC3 and autophagy, which is consistent with recent studies showing that EGFR suppresses autophagic cell death. Curcumin epidermal growth factor receptor Homo sapiens
4 The results show that EGFR is an Sp-regulated gene in bladder cancer, and drugs such as BA and curcumin that repress Sp proteins also ablate EGFR expression. Curcumin epidermal growth factor receptor Homo sapiens
5 The results show that EGFR is an Sp-regulated gene in bladder cancer, and drugs such as BA and curcumin that repress Sp proteins also ablate EGFR expression. Curcumin epidermal growth factor receptor Homo sapiens
6 Thus, compounds such as curcumin and BA that downregulate Sp transcription factors represent a novel class of anticancer drugs that target EGFR in bladder cancer cells and tumors by inhibiting receptor expression. Curcumin epidermal growth factor receptor Homo sapiens