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Horizontal transfer of whole mitochondria restores tumorigenic potential in mitochondria! DNA-deficient cancer cells

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F86652036%3A_____%2F17%3A00474268" target="_blank" >RIV/86652036:_____/17:00474268 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/17:00474268 RIV/00216208:11310/17:10359229

  • Result on the web

    <a href="http://dx.doi.org/10.7554/eLife.22187" target="_blank" >http://dx.doi.org/10.7554/eLife.22187</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.7554/eLife.22187" target="_blank" >10.7554/eLife.22187</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Horizontal transfer of whole mitochondria restores tumorigenic potential in mitochondria! DNA-deficient cancer cells

  • Original language description

    Recently, we showed that generation of tumours in syngeneic mice by cells devoid of mitochondrial (mt) DNA (rho(0) cells) is linked to the acquisition of the host mtDNA. However, the mechanism of mtDNA movement between cells remains unresolved. To determine whether the transfer of mtDNA involves whole mitochondria, we injected B16 rho(0) mouse melanoma cells into syngeneic C576116N(su9DsRed2) mice that express red fluorescent protein in their mitochondria. We document that mtDNA is acquired by transfer of whole mitochondria from the host animal, leading to normalisation of mitochondrial respiration. Additionally, knockdown of key mitochondrial complex I (NDUFV1) and complex II (SDHC) subunits by shRNA in B16 rho(0) cells abolished or significantly retarded their ability to form tumours. Collectively, these results show that intact mitochondria with their mtDNA payload are transferred in the developing tumour, and provide functional evidence for an essential role of oxidative phosphorylation in cancer.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    eLife

  • ISSN

    2050-084X

  • e-ISSN

  • Volume of the periodical

    6

  • Issue of the periodical within the volume

    15 Febr 2017

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    22

  • Pages from-to

  • UT code for WoS article

    000397644600001

  • EID of the result in the Scopus database

    2-s2.0-85016312406