Autophagy in malignant transformation and cancer progression

Lorenzo Galluzzi, Federico Pietrocola, José Manuel Bravo-San Pedro, Ravi K. Amaravadi, Eric H. Baehrecke, Francesco Cecconi, Patrice Codogno, Jayanta Debnath, David A. Gewirtz, Vassiliki Karantza, Alec Kimmelman, Sharad Kumar, Beth Levine, Maria Chiara Maiuri, Seamus J. Martin, Josef Penninger, Mauro Piacentini, David C. Rubinsztein, Hans Uwe Simon, Anne SimonsenAndrew M. Thorburn, Guillermo Velasco, Kevin M. Ryan, Guido Kroemer

    Research output: Contribution to journalArticlepeer-review

    1011 Citations (Scopus)

    Abstract

    Autophagy plays a key role in the maintenance of cellular homeostasis. In healthy cells, such a homeostatic activity constitutes a robust barrier against malignant transformation. Accordingly, many oncoproteins inhibit, and several oncosuppressor proteins promote, autophagy. Moreover, autophagy is required for optimal anticancer immunosurveillance. In neoplastic cells, however, autophagic responses constitute a means to cope with intracellular and environmental stress, thus favoring tumor progression. This implies that at least in some cases, oncogenesis proceeds along with a temporary inhibition of autophagy or a gain of molecular functions that antagonize its oncosuppressive activity. Here, we discuss the differential impact of autophagy on distinct phases of tumorigenesis and the implications of this concept for the use of autophagy modulators in cancer therapy. Autophagy has been described to have tumor-suppressive as well as tumor-promoting functions. This review discusses how stage and context alters the role for autophagy in cancer, and argues for further research prior to targeting autophagy in cancer therapy.

    Original languageEnglish
    Pages (from-to)856-880
    Number of pages25
    JournalEMBO Journal
    Volume34
    Issue number7
    DOIs
    Publication statusPublished - 1 Apr 2015

    Keywords

    • Adaptive stress responses
    • Beclin 1
    • KRAS
    • inflammation
    • mitophagy

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