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Cited by 812

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Dose‐dependent induction of apoptosis in human tumour cell lines by widely diverging stimuli

Lennon, S. V., Martin, S. J., Cotter, T. G.·1991·Cell Proliferation

Abstract

Abstract. Cell death may occur by either of two mechanisms: apoptosis or necrosis. Necrosis, the first type of cell death to be recognized, is an uncontrolled degenerative phenomenon invariably caused by noxious stimuli and is the result of irreversible failure of membrane function. Apoptosis, on the other hand, is a death process which involves a series of well‐organized events which require active cell participation, and is primarily caused by physiological stimuli. In the present study we show that cell death induced by a range of varied agents may take the form of either apoptosis or necrosis. Apoptotic cell death was found to occur at low levels of these agents, while at higher levels necrosis occurred. Hence, cells which are not killed directly, but merely injured by these agents, have the capacity to activate an internally programmed suicide death mechanism, whereas cells receiving greater injuries apparently do not. In addition, the presence of extracellular calcium was found to be necessary for the induction of apoptosis with all agents tested.

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Crossref · 10.1111/j.1365-2184.1991.tb01150.x

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Metadata

Authors
Lennon, S. V., Martin, S. J., & Cotter, T. G.
Venue
Cell Proliferation
Publisher
Wiley
Published
1991-03
Volume
24
Issue
2
Pages
203-214
ISSN
  • 0960-7722 (ISSN-L)
  • 1365-2184
OpenAlex
W2007861801
Cited by
812
References
0
FWCI
8.63
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Dose‐dependent induction of apoptosis in human tumour cell lines by widely diverging stimuli. https://app.cochat.ai/papers/10.1111/j.1365-2184.1991.tb01150.x
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Lennon, S. V., Martin, S. J., & Cotter, T. G. (1991). Dose‐dependent induction of apoptosis in human tumour cell lines by widely diverging stimuli. Cell Proliferation. https://doi.org/10.1111/j.1365-2184.1991.tb01150.x

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.