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Autophagy, an Achilles' heel AKTing against cancer?
Michael Degtyarev1, Ann De Mazière, Judith Klumperman
1Department of Cancer Signaling and Translational Oncology, Genentech Inc., 1 DNA Way, South San Francisco, CA 94080, USA.
Abstract:
Akt has emerged as an attractive cancer therapeutic target with a central role in cell survival, growth, proliferation and metabolism.A key to the clinical success of Akt inhibitors is the maximal possible antitumor efficacy achievable without intolerable side effects. In our recent work, we show that although Akt inhibition does not always induce a clear apoptotic response, autophagy is a more readily detectable response to pan-Akt knockdown or selective small molecule inhibitors of the PI3K/Akt pathway. Autophagy isa catabolic process of bulk lysosomal degradation and recycling of cytoplasmic material and organelles, which can provide a temporary survival mechanism for cells under stress conditions, but can also make cells vulnerable to several forms of cell death under specific circumstances. We hypothesize that autophagy induced by Akt inhibition may sensitize tumor cells to agents targeting the later steps of this lysosomal degradation process. Indeed, agents that interfere with the lysosomal degradation function could precipitate cell death when combined with Akt inhibition and promote complete tumor remissions in preclinical models. These findings suggest that manipulating the autophagic response may be a promising strategy to increase the therapeutic efficacy of Akt inhibitors.
Insights
Akt inhibition triggers autophagy, a cellular recycling process, which can sensitize cancer cells. Combining Akt inhibitors with agents targeting lysosomal degradation promotes tumor remission, enhancing therapeutic efficacy.
Area of Science:
- Oncology
- Molecular Biology
- Cellular Biology
Background:
- The Akt signaling pathway is crucial for cancer cell survival, growth, proliferation, and metabolism.
- Akt inhibitors are promising cancer therapeutics, but maximizing antitumor efficacy while minimizing side effects is key.
Purpose of the Study:
- To investigate the role of autophagy in response to Akt inhibition.
- To explore the potential of combining Akt inhibitors with lysosomal degradation inhibitors for enhanced cancer therapy.
Main Methods:
- Utilized pan-Akt knockdown and selective PI3K/Akt pathway small molecule inhibitors.
- Assessed autophagy as a response to Akt inhibition.
- Tested combination therapies of Akt inhibitors with agents targeting lysosomal degradation in preclinical cancer models.
Main Results:
- Akt inhibition readily induces autophagy, rather than apoptosis, in cancer cells.
- Combining Akt inhibition with lysosomal degradation inhibitors leads to cancer cell death.
- This combination therapy achieved complete tumor remissions in preclinical models.
Conclusions:
- Autophagy induction is a significant response to Akt inhibition.
- Targeting lysosomal degradation in combination with Akt inhibitors enhances anti-tumor efficacy.
- Manipulating autophagy presents a promising strategy to improve Akt inhibitor-based cancer therapies.
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