Difference between revisions of "Sharma 2021 Cancer Cell Int"
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|title=Sharma P, Sharma V, Ahluwalia TS, Dogra N, Kumar S, Singh S (2021) Let-7a induces metabolic reprogramming in breast cancer cells via targeting mitochondrial encoded ND4. Cancer Cell Int 21:629. | |title=Sharma P, Sharma V, Ahluwalia TS, Dogra N, Kumar S, Singh S (2021) Let-7a induces metabolic reprogramming in breast cancer cells via targeting mitochondrial encoded ND4. Cancer Cell Int 21:629. | ||
|info=[https://www.ncbi.nlm.nih.gov/pubmed/34838007 PMID: 34838007 Open Access] | |info=[https://www.ncbi.nlm.nih.gov/pubmed/34838007 PMID: 34838007 Open Access] | ||
|authors=Sharma | |authors=Sharma Praveen, Sharma Vibhuti, Ahluwalia Tarunveer Singh, Dogra Nilambra, Kumar Santosh, Singh Sandeep | ||
|year=2021 | |year=2021 | ||
|journal=Cancer Cell Int | |journal=Cancer Cell Int | ||
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These findings uncover a novel mechanism by which mitomiR regulates mitochondrial transcription. | These findings uncover a novel mechanism by which mitomiR regulates mitochondrial transcription. | ||
|keywords=Cancer, Glycolysis, Metabolic reprogramming, Mito-miRs, Mitochondria | |||
|editor=[[Plangger M]] | |editor=[[Plangger M]] | ||
}} | }} | ||
{{Labeling | {{Labeling | ||
|area=Respiration | |area=Respiration, mtDNA;mt-genetics | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|additional=2021-11 | |additional=2021-11 | ||
}} | }} | ||
Revision as of 19:29, 30 November 2021
| Sharma P, Sharma V, Ahluwalia TS, Dogra N, Kumar S, Singh S (2021) Let-7a induces metabolic reprogramming in breast cancer cells via targeting mitochondrial encoded ND4. Cancer Cell Int 21:629. |
Sharma Praveen, Sharma Vibhuti, Ahluwalia Tarunveer Singh, Dogra Nilambra, Kumar Santosh, Singh Sandeep (2021) Cancer Cell Int
Abstract: MicroRNA (miRNA) that translocate from the nucleus to mitochondria are referred to as mitochondrial microRNA (mitomiR). Albeit mitomiRs have been shown to modulate gene expression, their functional impact within mitochondria is unknown. The main objective of this study is to investigate whether the mitochondrial genome is regulated by miR present inside the mitochondria.
Here, we report mitomiR let-7a regulates mitochondrial transcription in breast cancer cells and reprogram the metabolism accordingly. These effects were mediated through the interaction of let-7a with mtDNA, as studied by RNA pull-down assays, altering the activity of Complex I in a cell line-specific manner. Our study, for the first time, identifies the role of mitomiR (let-7a) in regulating the mitochondrial genome by transcriptional repression and its contribution to regulating mitochondrial metabolism of breast cancer cells.
These findings uncover a novel mechanism by which mitomiR regulates mitochondrial transcription. • Keywords: Cancer, Glycolysis, Metabolic reprogramming, Mito-miRs, Mitochondria • Bioblast editor: Plangger M
Labels: MiParea: Respiration, mtDNA;mt-genetics
HRR: Oxygraph-2k
2021-11
