Abstract |
A number of viral and eukaryotic proteins which undergo a lipophilic modification by the enzyme N-myristoyltransferase (NMT: NMT1 and NMT2) are required for signal transduction and regulatory functions. To investigate whether NMT2 contributes to the pathogenesis of colorectal carcinoma, we observed a higher expression of NMT2 in most of the cases of cancerous tissues compared to normal tissues (84.6% of cases; P < 0.05) by Western blot analysis. Furthermore, protein- protein interaction of NMTs revealed that m-calpain interacts with NMT1 while caspase-3 interacts with NMT2. Our findings provide the first evidence of higher expression of NMT2 in human colorectal adenocarcinomas and the interaction of both forms of NMT with various signaling molecules.
|
Authors | Ponniah Selvakumar, Erin Smith-Windsor, Keith Bonham, Rajendra K Sharma |
Journal | FEBS letters
(FEBS Lett)
Vol. 580
Issue 8
Pg. 2021-6
(Apr 03 2006)
ISSN: 0014-5793 [Print] England |
PMID | 16530191
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Proto-Oncogene Proteins c-bcl-2
- Tumor Suppressor Protein p53
- Acyltransferases
- glycylpeptide N-tetradecanoyltransferase
- Peptide Hydrolases
- Calpain
- Caspases
|
Topics |
- Acyltransferases
(metabolism)
- Calpain
(metabolism)
- Caspases
(metabolism)
- Colonic Neoplasms
(enzymology, metabolism)
- Gene Expression Regulation, Neoplastic
- Humans
- Peptide Hydrolases
(metabolism)
- Protein Binding
- Proto-Oncogene Proteins c-bcl-2
(metabolism)
- Tumor Cells, Cultured
- Tumor Suppressor Protein p53
(metabolism)
|