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We began analyzing https://www.nature.com/articles/s41467-018-04070-6, but it redirected us to https://www.nature.com/articles/s41467-018-04070-6. The analysis below is for the second page.

Title[redir]:
Autophagy promotes the survival of dormant breast cancer cells and metastatic tumour recurrence | Nature Communications
Description:
Cancer recurrence after initial diagnosis and treatment is a major cause of breast cancer (BC) mortality, which results from the metastatic outbreak of dormant tumour cells. Alterations in the tumour microenvironment can trigger signalling pathways in dormant cells leading to their proliferation. However, processes involved in the initial and the long-term survival of disseminated dormant BC cells remain largely unknown. Here we show that autophagy is a critical mechanism for the survival of disseminated dormant BC cells. Pharmacologic or genetic inhibition of autophagy in dormant BC cells results in significantly decreased cell survival and metastatic burden in mouse and human 3D in vitro and in vivo preclinical models of dormancy. In vivo experiments identify autophagy gene autophagy-related 7 (ATG7) to be essential for autophagy activation. Mechanistically, inhibition of the autophagic flux in dormant BC cells leads to the accumulation of damaged mitochondria and reactive oxygen species (ROS), resulting in cell apoptosis. Highly metastatic dormant cancer cells contribute to breast cancer recurrence, but the underlying mechanism is less understood. Here, the authors show that dormant breast cancer cells depend on autophagy to ensure their long term survival and distant recurrence

Matching Content Categories {๐Ÿ“š}

  • Science
  • Education
  • Health & Fitness

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Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

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๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


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Keywords {๐Ÿ”}

cells, autophagy, bme, dormant, hcq, metastatic, day, fig, cell, pubmed, article, cancer, days, inhibition, google, scholar, culture, treatment, cas, data, tumour, treated, mice, comparisons, mitochondrial, col, sem, burden, compared, proliferative, supplementary, matrices, nature, survival, lung, assay, central, analysis, dormancy, vivo, fibrosis, results, twosided, autophagic, proliferation, significantly, vitro, observed, expression, wells,

Topics {โœ’๏ธ}

/product-category/physiologic-cell-culture/extracellular-matrix-proteins/ nature portfolio privacy policy andalusian regional ministry intramural research program thermo scientific anti-cyclophillin proliferative index determined advertising nature 529 nature tandem reporter mcherry-gfp-lc3 reprints col-i-enriched fibrotic environment thermo fisher scientific research cd1nu/nu athymic mice isolate mcherry-gfp-lc3 d2 article vera-ramirez cdnu/nu athymic mice mannโ€“whitney u-test tandem fluorescent-tagged lc3 library preparation cd1nu/nu mice injected adenovector-mediated gene transfer mcherry-gfp-lc3 cells showed mcherry-gfp-lc3 cells isolated 50โ€‰mg/kg body weight mcherry-gfp-lc3 cells grown social media complete media genitourinary medical oncology park2/parkin-dependent mitophagy mda-mb-231 cell lines initial orga-specific metastasis cytotox-glo cytoxocity assay frequent post-translational modifications develop oxidative-based therapies double-positive puncta permissions total tumour burden/lung mda-mb-231 viable cells full size image original author mcherry-gfp-lc3 cells lipidated form lc3-ii average tumour burden/lung adenovirus-null vector control ros-induced cell death murine mammary neoplasia injectedย d2a1-gfp cells

Schema {๐Ÿ—บ๏ธ}

WebPage:
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         headline:Autophagy promotes the survival of dormant breast cancer cells and metastatic tumour recurrence
         description:Cancer recurrence after initial diagnosis and treatment is a major cause of breast cancer (BC) mortality, which results from the metastatic outbreak of dormant tumour cells. Alterations in the tumour microenvironment can trigger signalling pathways in dormant cells leading to their proliferation. However, processes involved in the initial and the long-term survival of disseminated dormant BC cells remain largely unknown. Here we show that autophagy is a critical mechanism for the survival of disseminated dormant BC cells. Pharmacologic or genetic inhibition of autophagy in dormant BC cells results in significantly decreased cell survival and metastatic burden in mouse and human 3D in vitro and in vivo preclinical models of dormancy. In vivo experiments identify autophagy gene autophagy-related 7 (ATG7) to be essential for autophagy activation. Mechanistically, inhibition of the autophagic flux in dormant BC cells leads to the accumulation of damaged mitochondria and reactive oxygen species (ROS), resulting in cell apoptosis. Highly metastatic dormant cancer cells contribute to breast cancer recurrence, but the underlying mechanism is less understood. Here, the authors show that dormant breast cancer cells depend on autophagy to ensure their long term survival and distant recurrence
         datePublished:2018-05-22T00:00:00Z
         dateModified:2018-05-22T00:00:00Z
         pageStart:1
         pageEnd:12
         license:http://creativecommons.org/licenses/by/4.0/
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            Mitophagy
            Science
            Humanities and Social Sciences
            multidisciplinary
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      headline:Autophagy promotes the survival of dormant breast cancer cells and metastatic tumour recurrence
      description:Cancer recurrence after initial diagnosis and treatment is a major cause of breast cancer (BC) mortality, which results from the metastatic outbreak of dormant tumour cells. Alterations in the tumour microenvironment can trigger signalling pathways in dormant cells leading to their proliferation. However, processes involved in the initial and the long-term survival of disseminated dormant BC cells remain largely unknown. Here we show that autophagy is a critical mechanism for the survival of disseminated dormant BC cells. Pharmacologic or genetic inhibition of autophagy in dormant BC cells results in significantly decreased cell survival and metastatic burden in mouse and human 3D in vitro and in vivo preclinical models of dormancy. In vivo experiments identify autophagy gene autophagy-related 7 (ATG7) to be essential for autophagy activation. Mechanistically, inhibition of the autophagic flux in dormant BC cells leads to the accumulation of damaged mitochondria and reactive oxygen species (ROS), resulting in cell apoptosis. Highly metastatic dormant cancer cells contribute to breast cancer recurrence, but the underlying mechanism is less understood. Here, the authors show that dormant breast cancer cells depend on autophagy to ensure their long term survival and distant recurrence
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      name:Laboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, USA
      name:Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, USA
      name:Laboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, USA
      name:Laboratory of Cancer Biology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, USA

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