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Cited by 307

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Cell death by autophagy: emerging molecular mechanisms and implications for cancer therapy

Open access
Fulda, S, Kögel, D·2015·Oncogene

Abstract

Autophagy is a tightly-regulated catabolic process of cellular self-digestion by which cellular components are targeted to lysosomes for their degradation. Key functions of autophagy are to provide energy and metabolic precursors under conditions of starvation and to alleviate stress by removal of damaged proteins and organelles, which are deleterious for cell survival. Therefore, autophagy appears to serve as a pro-survival stress response in most settings. However, the role of autophagy in modulating cell death is highly dependent on the cellular context and its extent. There is an increasing evidence for cell death by autophagy, in particular in developmental cell death in lower organisms and in autophagic cancer cell death induced by novel cancer drugs. The death-promoting and -executing mechanisms involved in the different paradigms of autophagic cell death (ACD) are very diverse and complex, but a draft scenario of the key molecular targets involved in ACD is beginning to emerge. This review provides an up-to-date and comprehensive report on the molecular mechanisms of drug-induced autophagy-dependent cell death and highlights recent key findings in this exciting field of research.

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Metadata

Authors
Fulda, S., & Kögel, D.
Venue
Oncogene
Published
2015-01-26
Volume
34
Issue
40
Pages
5105-5113
ISSN
  • 0950-9232 (ISSN-L)
  • 1476-5594
OpenAlex
W2052419480
Cited by
307
References
9
FWCI
29.13
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: Cell death by autophagy: emerging molecular mechanisms and implications for cancer therapy. https://app.cochat.ai/papers/10.1038/onc.2014.458
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Fulda, S., & Kögel, D. (2015). Cell death by autophagy: emerging molecular mechanisms and implications for cancer therapy. Oncogene. https://doi.org/10.1038/onc.2014.458

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