2000
DOI: 10.1006/excr.1999.4759
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Detection of Apoptosis Induced by Topoisomerase Inhibitors and Serum Deprivation in Syrian Hamster Embryo Cells

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Cited by 29 publications
(17 citation statements)
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“…However, no PARP cleavage product could be detected in A549 cells that were treated with either free or HDL 3 -associated aTS. Similar observations were reported for Syrian hamster embryo cells that underwent apoptosis (characterized by pronounced DNA fragmentation) in response to topoisomerase inhibitor treatment or serum deprivation [47]. Results obtained during the present study appear to be specific for aTS, as the 86-kDa PARP cleavage product is formed in A549 cells in response to MAL-induced apoptosis [48].…”
Section: Suppression Of Tumor Growth By a Ats In Vivosupporting
confidence: 74%
“…However, no PARP cleavage product could be detected in A549 cells that were treated with either free or HDL 3 -associated aTS. Similar observations were reported for Syrian hamster embryo cells that underwent apoptosis (characterized by pronounced DNA fragmentation) in response to topoisomerase inhibitor treatment or serum deprivation [47]. Results obtained during the present study appear to be specific for aTS, as the 86-kDa PARP cleavage product is formed in A549 cells in response to MAL-induced apoptosis [48].…”
Section: Suppression Of Tumor Growth By a Ats In Vivosupporting
confidence: 74%
“…Interestingly, PARP degradation with no appearance of its 85-kDa fragment is found in apoptotic Syrian hamster embryo (SHE) cells (Alexandre et al, 2000a). No induction of caspase-3 activity was noted in apoptotic SHE cells (Alexandre et al, 2000b). These results along with the data presented in Figures 3 and 4d suggest that although PARP is the common substrate of some caspases, proteases other than caspase-3 (such as caspase-7) may degrade PARP without its 85-kDa fragment that is typically seen in caspase-3-mediated PARP cleavage.…”
Section: Discussionmentioning
confidence: 99%
“…Cell culture systems sensitive for serum withdrawal can be subdivided in two groups by their rate of apoptotic response. A rapid time course of apoptosis within a few hours is described for undifferentiated PC-12 cells [1], AKR-2B mouse fibroblasts [2], Syrian hamster embryo cells [3], and myocardiacs [4], for example. A slow time course, which may take several days, was described for NGF-differentiated PC-12 cells [1], HUVEC [5] and myc-overexpressing Rat-1 cells [6], for example.…”
Section: Introductionmentioning
confidence: 98%