| Literature DB >> 12706875 |
Miho Ueda1, Satoshi Kokura, Eiko Imamoto, Yuji Naito, Osamu Handa, Tomohisa Takagi, Norimasa Yoshida, Toshikazu Yoshikawa.
Abstract
The transcription factor NF-kappaB is constitutively activated in many human cancers and induces the expression of multiple genes, including those of anti-apoptotic proteins. This study investigated the mechanism by which human gastric cancer cells (MKN45) are resistant to apoptosis induced by tumor necrosis factor alpha (TNF-alpha). Confluent monolayers of MKN45 cells were either pretreated or not for 60 min with PSI, a peptide aldehyde known to specifically inhibit the chymotrypsin-like activity of 26S proteasome. Cells were subsequently stimulated with recombinant human TNF-alpha, and cell viabilities were determined by the WST-1 assay. Apoptosis was confirmed by fluorescence microscopy after staining with Hoechst 33342, and DNA fragmentation was determined by a DNA fragmentation detection kit. A 24-h incubation with either TNF-alpha or PSI alone did not affect cell viabilities; however, pretreatment with PSI significantly enhanced the level of apoptosis induced by TNF-alpha. Therefore, this study suggests the possibility that blocking of NF-kappaB activity renders gastric cancer cells susceptible to the apoptosis induced by TNF-alpha.Entities:
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Year: 2003 PMID: 12706875 DOI: 10.1016/s0304-3835(03)00002-8
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679