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Inhibition of NF-kappaB activation and chemokine expression by the leukocyte glycoprotein, CD43, in colon cancer cells.

Artikel i vetenskaplig tidskrift
Författare Sirle Laos
Dan Baeckström
Gunnar C. Hansson
Publicerad i International journal of oncology
Volym 28
Nummer/häfte 3
Sidor 695-704
ISSN 1019-6439
Publiceringsår 2006
Publicerad vid Institutionen för biomedicin, avdelningen för medicinsk kemi och cellbiologi
Sidor 695-704
Språk en
Länkar www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Active Transport, Cell Nucleus, drug effects, Antigens, CD43, genetics, metabolism, Blotting, Western, Cell Line, Tumor, Cell Nucleus, drug effects, metabolism, Chemokine CCL2, genetics, metabolism, Chemokines, genetics, metabolism, Chemokines, CXC, genetics, metabolism, Colonic Neoplasms, genetics, metabolism, pathology, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Gene Expression Regulation, Neoplastic, genetics, Humans, I-kappa B Proteins, metabolism, Intercellular Signaling Peptides and Proteins, genetics, metabolism, Interleukin-8, genetics, metabolism, NF-kappa B, antagonists & inhibitors, genetics, metabolism, PPAR gamma, metabolism, RNA, Messenger, genetics, metabolism, Time Factors, Transcription Factor RelA, genetics, metabolism, Tumor Necrosis Factor-alpha, pharmacology
Ämneskategorier Medicin och Hälsovetenskap

Sammanfattning

CD43 is a heavily O-glycosylated type I trans-membrane protein, expressed at high levels on the surface of leukocytes. It is frequently overexpressed in early colon adenomas, but not in normal colon epithelial cells. To identify CD43 target genes, gene array analysis was performed using a tetracycline-inducible CD43 expression system in human colon adenocarcinoma SW480 cells. CD43 was demonstrated to down-regulate a variety of chemokine genes. Overexpression of CD43 suppressed constitutive as well as PMA-induced NF-kappaB activation and reduced the DNA binding of transcription factor p65 but not p50. Furthermore, a reduced NF-kappaB responsive promoter activity was observed and a decreased expression of proinflammatory chemokines MCP-1, IL-8 and GRO-alpha. These results suggest that overexpression of CD43 suppresses a subset of NF-kappaB target genes, partly via the inhibition of p65 transcriptional activity.

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