Abstract
Standard anti-proliferative chemotherapy is relatively ineffective against slowly proliferating androgen-independent prostate cancer cells within metastatic sites. In contrast, the lipophilic cytotoxin thapsigargin, which causes apoptosis by disrupting intracellular free Ca2+ levels, is effective against both proliferative and quiescent (i.e., G0-arrested) cells. However, thapsigargin's mechanism of action indicates that it is unlikely to be selective for cancer cells or prostate cells.
Originalsprog | Engelsk |
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Tidsskrift | National Cancer Institute. Journal (Online) |
Vol/bind | 95 |
Udgave nummer | 13 |
Sider (fra-til) | 990-1000 |
Antal sider | 11 |
ISSN | 1460-2105 |
Status | Udgivet - 2 jul. 2003 |