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Kaiso interacts with p120-catenin to regulate β-catenin expression at the transcriptional level.

AbstractBACKGROUND:
We have reported that p120-catenin could regulate β-catenin transcription in lung cancer cells, but the specific mechanism is unclear.
METHODS AND RESULTS:
In this study, bisulfite sequencing PCR showed that the β-catenin promoter region in SPC-A-1 and LTEP-a-2 lung cancer cell lines has Kaiso binding sites sequences and CpG islands which may combine with Kaiso. The demethylating reagent 5-Aza-2'-deoxycytidine significantly upregulated β-catenin mRNA expression in lung cancer cell lines, whereas expression was significantly reduced following transfection with Kaiso. However, the upregulation of β-catenin mRNA expression after treatment with 5-Aza-2'-deoxycytidine was not reduced by subsequent transfection with Kaiso cDNA. Chromatin immunoprecipitation showed that, in lung cancer cell lines, methylated CpG-dinucleotides sequences combined with Kaiso and the Kaiso binding sites sequence did not. The capacity of Kaiso to combine with p120-catenin isoforms was confirmed by immunoprecipitation.
CONCLUSIONS:
Based on these results, we concluded that Kaiso participates in the regulation by p120ctn of β-catenin mRNA expression in the lung cancer cell lines.
AuthorsYang Liu, Qian-Ze Dong, Si Wang, Hong-Tao Xu, Yuan Miao, Liang Wang, En-Hua Wang
JournalPloS one (PLoS One) Vol. 9 Issue 2 Pg. e87537 ( 2014) ISSN: 1932-6203 [Electronic] United States
PMID24498333 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Catenins
  • Enzyme Inhibitors
  • Transcription Factors
  • ZBTB33 protein, human
  • beta Catenin
  • Decitabine
  • Azacitidine
  • Delta Catenin
  • CTNND1 protein, human
Topics
  • Azacitidine (analogs & derivatives, pharmacology)
  • Blotting, Western
  • Catenins (genetics, metabolism)
  • Cell Line, Tumor
  • CpG Islands (genetics)
  • DNA Methylation
  • Decitabine
  • Enzyme Inhibitors (pharmacology)
  • Gene Expression Regulation, Neoplastic (drug effects)
  • Humans
  • Lung Neoplasms (genetics, metabolism, pathology)
  • Promoter Regions, Genetic (genetics)
  • Protein Binding
  • Reverse Transcriptase Polymerase Chain Reaction
  • Transcription Factors (genetics, metabolism)
  • Transcription, Genetic
  • Up-Regulation (drug effects)
  • beta Catenin (genetics, metabolism)
  • Delta Catenin

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