A cytoskeleton-associated protein, TMAP/CKAP2, is involved in the proliferation of human foreskin fibroblasts
Creators
- 1. Department of Molecular Cell Biology and Samsung Biomedical Research Institute, Sungkyunkwan University School of Medicine, Suwon (Korea, Republic of)
- 2. Department of Biochemistry, Dankook University College of Medicine, Chunan (Korea, Republic of)
Description
Previously, we reported the cloning of a cytoskeleton-associated protein, TMAP/CKAP2, which was up-regulated in primary human gastric cancers. Although TMAP/CKAP2 has been found to be expressed in most cancer cell lines examined, the function of CKAP2 is not known. In this study, we found that TMAP/CKAP2 was not expressed in G0/G1 arrested HFFs, but that it was expressed in actively dividing cells. After initiating the cell cycle, TMAP/CKAP2 levels remained low throughout most of the G1 phase, but gradually increased between late G1 and G2/M. Knockdown of TMAP/CKAP2 reduced pRB phosphorylation and increased p27 expression, and consequently reduced HFF proliferation, whereas constitutive TMAP/CKAP2 expression increased pRB phosphorylation and enhanced proliferation. Our results show that this novel cytoskeleton-associated protein is expressed cell cycle dependently and that it is involved in cell proliferation
Additional details
Identifiers
- DOI
- 10.1016/j.bbrc.2006.07.046;
- PII
- S0006-291X(06)01584-1;
Publishing Information
- Journal Title
- Biochemical and Biophysical Research Communications
- Journal Volume
- 348
- Journal Issue
- 1
- Journal Page Range
- p. 222-228
- ISSN
- 0006-291X
- CODEN
- BBRCA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38027452
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CELL CYCLE; CELL PROLIFERATION; CLONING; FIBROBLASTS; MICROTUBULES; NEOPLASMS; PHOSPHORYLATION; PROTEINS
- Descriptors DEC
- ANIMAL CELLS; CELL CONSTITUENTS; CHEMICAL REACTIONS; CONNECTIVE TISSUE CELLS; DISEASES; ORGANIC COMPOUNDS; SOMATIC CELLS
Optional Information
- Copyright
- Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.