Reducing VDAC1 expression induces a non-apoptotic role for pro-apoptotic proteins in cancer cell differentiation
Tasleem Arif1, Yakov Krelin1, Varda Shoshan-Barmatz1
1Department of Life Sciences and the National Institute for Biotechnology in the Negev, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Abstract:
Proteins initially identified as essential for apoptosis also mediate a wide range of non-apoptotic functions that include cell cycle progression, differentiation and metabolism. As this phenomenon was mostly reported with non-cancer cells, we considered non-conventional roles for the apoptotic machinery in the cancer setting. We found that treating glioblastoma (GBM) tumors with siRNA against VDAC1, a mitochondrial protein found at the crossroads of metabolic and survival pathways and involved in apoptosis, inhibited tumor growth while leading to differentiation of tumor cells into neuronal-like cells, as reflected in the expression of specific markers. Although VDAC1 depletion did not induce apoptosis, the expression levels of several pro-apoptotic regulatory proteins were changed. Specifically, VDAC1 deletion led to up-regulation of caspases, p53, cytochrome c, and down-regulation of SMAC/Diablo, AIF and TSPO. The down-regulated group was highly expressed in U-87MG xenografts, as well as in GBMs from human patients. We also showed that the rewired cancer-cell metabolism resulting from VDAC1 depletion reinforced cell growth arrest and differentiation via alterations in the transcription factors p53, c-Myc, HIF-1α and NF-κB. The decrease in c-Myc, HIF-1α and NF-κB levels was in accord with reduced cell proliferation, whereas increased p53 expression promoted differentiation. Thus, upon metabolic re-programing induced by VDAC1 depletion, the levels of pro-apoptotic proteins associated with cell growth decreased, while those connected to cell differentiation increased, converting GBM cells into astrocyte- and neuron-like cells. The results reveal that in tumors, pro-apoptotic proteins can perform non-apoptotic functions, acting as regulators of cell growth and differentiation, making these molecules potential new targets for cancer therapy. This article is part of a Special Issue entitled 'EBEC 2016: 19th European Bioenergetics Conference, Riva del Garda, Italy, July 2-6, 2016', edited by Prof. Paolo Bernardi.
Insights
Targeting VDAC1 in glioblastoma (GBM) inhibits tumor growth and promotes differentiation into neuronal-like cells. This study reveals non-apoptotic roles for pro-apoptotic proteins in cancer, suggesting new therapeutic strategies.
Area of Science:
- Molecular Biology
- Cancer Research
- Cellular Metabolism
Background:
- Apoptosis-related proteins have non-apoptotic functions in cell cycle, differentiation, and metabolism, primarily studied in non-cancer cells.
- Investigating these non-conventional roles in cancer is crucial for understanding tumor biology and developing novel therapies.
- Glioblastoma (GBM) is an aggressive brain tumor with complex regulatory pathways.
Purpose of the Study:
- To explore non-apoptotic functions of apoptotic machinery in glioblastoma.
- To investigate the role of VDAC1 (voltage-dependent anion channel 1) in GBM tumor growth and differentiation.
- To identify potential new therapeutic targets within apoptotic regulatory proteins in cancer.
Main Methods:
- Treatment of glioblastoma tumors with siRNA targeting VDAC1.
- Analysis of tumor growth inhibition and cell differentiation markers.
- Assessment of expression levels of pro-apoptotic proteins (caspases, p53, cytochrome c, SMAC/Diablo, AIF, TSPO) and transcription factors (p53, c-Myc, HIF-1α, NF-κB).
Main Results:
- VDAC1 depletion inhibited glioblastoma tumor growth and induced differentiation into neuronal-like cells.
- VDAC1 depletion did not induce apoptosis but altered expression of apoptotic regulators, up-regulating caspases and p53, and down-regulating SMAC/Diablo, AIF, and TSPO.
- Metabolic reprogramming due to VDAC1 depletion altered transcription factors, leading to growth arrest and differentiation.
Conclusions:
- Pro-apoptotic proteins can exert non-apoptotic functions in glioblastoma, regulating cell growth and differentiation.
- VDAC1 plays a critical role in metabolic pathways and survival, making it a potential therapeutic target.
- Targeting VDAC1 offers a novel strategy for glioblastoma treatment by inducing differentiation rather than apoptosis.
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