DEP-1 protein tyrosine phosphatase inhibits proliferation and migration of colon carcinoma cells and is upregulated by protective nutrients

Autor: K K Balavenkatraman, Frank-D. Böhmer, Beatrice L. Pool-Zobel, T Kautenburger, Karlheinz Friedrich, E Jandt, Arne Östman
Rok vydání: 2006
Předmět:
Cancer Research
Transcription
Genetic

Protein tyrosine phosphatase
medicine.disease_cause
Cell Movement
Protein Phosphatase 1
RNA
Neoplasm

RNA
Small Interfering

Cells
Cultured

Receptor-Like Protein Tyrosine Phosphatases
Class 3

Cell migration
respiratory system
Cell biology
Neoplasm Proteins
Up-Regulation
Butyrates
Biochemistry
Enzyme Induction
Malus
Colonic Neoplasms
RNA Interference
Chemokines
CXC

Cell Division
Adenoma
Colon
Recombinant Fusion Proteins
Phosphatase
Down-Regulation
Butyrate
Biology
Adenocarcinoma
Transfection
complex mixtures
Phenols
Cell Line
Tumor

Genetics
medicine
Anticarcinogenic Agents
Humans
RNA
Messenger

Molecular Biology
Flavonoids
Tea
Cell growth
Plant Extracts
Polyphenols
Protein phosphatase 1
Epithelial Cells
Chemokine CXCL12
respiratory tract diseases
Cell culture
Lysophospholipids
Protein Tyrosine Phosphatases
Carcinogenesis
Zdroj: Oncogene. 25(47)
ISSN: 0950-9232
Popis: The transmembrane protein-tyrosine phosphatase (PTP) DEP-1 (density-enhanced phosphatase) is a candidate tumor suppressor in the colon epithelium. We have explored the function of DEP-1 in colon epithelial cells by inducible re-expression in a DEP-1-deficient human colon cancer cell line. Density-enhanced phosphatase-1 re-expression led to profound inhibition of cell proliferation and cell migration, and was associated with cytoskeletal rearrangements. These effects were dependent on the PTP activity of DEP-1 as they were not observed with cells expressing the catalytically inactive DEP-1 C1239S variant. shRNA-mediated suppression of DEP-1 in a colon epithelial cell line with high endogenous DEP-1 levels enhanced proliferation, further supporting the antiproliferative function of DEP-1. Nutrients, which are considered to be chemoprotective with respect to colon cancer development, including butyrate, green tea and apple polyphenols, had the capacity to elevate transcription of endogenous DEP-1 mRNA and expression of DEP-1 protein. Upregulation of DEP-1 expression, and in turn inhibition of cell growth and migration may present a previously unrecognized mechanism of chemoprevention by nutrients.
Databáze: OpenAIRE