Abstract
At odds with historical views suggesting that mitochondrial functions are largely dispensable for cancer cells, it is now clear that mitochondria have a major impact on malignant transformation, tumor progression and response to treatment. Mitochondria are indeed critical for neoplastic cells not only as an abundant source of ATP and other metabolic intermediates, but also as gatekeepers of apoptotic cell death and inflammation. Interestingly, while mitochondrial components are mostly encoded by nuclear genes, mitochondria contain a small, circular genome that codes for a few mitochondrial proteins, ribosomal RNAs and transfer RNAs. Here, we describe a straightforward method to generate transmitochondrial cybrids, i.e., cancer cells depleted of their mitochondrial DNA and reconstituted with intact mitochondria from another cellular source. Once established, transmitochondrial cybrids can be stably propagated and are valuable to dissect the specific impact of the mitochondrial genome on cancer cell functions.
| Original language | English |
|---|---|
| Title of host publication | Immuno-oncology and immunotherapy - Part A |
| Publisher | Academic Press Inc. |
| Pages | 23-40 |
| Number of pages | 18 |
| Volume | 189 |
| ISBN (Print) | 9780443296222 |
| DOIs | |
| State | Published - Jan 2024 |
| Externally published | Yes |
Publication series
| Name | Methods in cell biology |
|---|---|
| ISSN (Print) | 0091-679X |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Cell Line, Tumor
- DNA, Mitochondrial/genetics
- Genome, Mitochondrial
- Humans
- Hybrid Cells
- Mitochondria/metabolism
- Neoplasms/pathology
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