Title : Sulforaphane counteracts aggressiveness of pancreatic cancer driven by dysregulated Cx43-mediated gap junctional intercellular communication.

Pub. Date : 2014 Mar 30

PMID : 24742583






4 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Sulforaphane counteracts aggressiveness of pancreatic cancer driven by dysregulated Cx43-mediated gap junctional intercellular communication. sulforaphane gap junction protein alpha 1 Homo sapiens
2 The bioactive substance sulforaphane enhanced Cx43 and E-cadherin levels, inhibited the CSC markers c-Met and CD133, improved the functional morphology of GJs and enhanced GJIC. sulforaphane gap junction protein alpha 1 Homo sapiens
3 Sulforaphane altered the phosphorylation of several kinases and their substrates and inhibition of GSK3, JNK and PKC prevented sulforaphane-induced CX43 expression. sulforaphane gap junction protein alpha 1 Homo sapiens
4 The sulforaphane-mediated expression of Cx43 was not correlated with enhanced Cx43 RNA expression, acetylated histone binding and Cx43 promoter de-methylation, suggesting that posttranslational phosphorylation is the dominant regulatory mechanism. sulforaphane gap junction protein alpha 1 Homo sapiens