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LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Questions
  9. Schema
  10. External Links
  11. Analytics And Tracking
  12. Libraries
  13. CDN Services

We are analyzing https://link.springer.com/article/10.1007/s40139-017-0139-5.

Title:
Autophagy and Ferroptosis—What Is the Connection? | Current Pathobiology Reports
Description:
Purpose of Review Autophagy is a conserved intracellular degradation system and plays a dual role in cell death, depending on context and phase. Ferroptosis is a new form of regulated cell death that mainly depends on iron accumulation and lipid peroxidation. In this review, we summarize the processes of autophagy and ferroptosis and discuss their crosstalk mechanisms at the molecular level. Recent Findings The original study shows that ferroptosis is morphologically, biochemically, and genetically distinct from autophagy and other types of cell death. However, recent studies demonstrate that activation of ferroptosis is indeed dependent on the induction of autophagy. Additionally, many ferroptosis regulators such as SLC7A11, GPX4, NRF2, p53, HSPB1, CISD1, FANCD2, and ACSL4 have been identified as potential regulators of autophagy. Summary This review not only highlights the importance of autophagy as an emerging mechanism of ferroptosis but also raises new insights regarding regulated cell death.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Telecommunications
  • Science

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 8,170,236 visitors per month in the current month.

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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

Not every website is profit-driven; some are created to spread information or serve as an online presence. Websites can be made for many reasons. This could be one of them. Link.springer.com could be secretly minting cash, but we can't detect the process.

Keywords {🔍}

pubmed, article, scholar, google, cas, cell, ferroptosis, autophagy, central, death, importance, cancer, study, regulation, demonstrated, kang, cells, tang, biol, nat, sun, lipid, acsl, xie, journal, daolin, regulated, protein, song, res, yang, chem, chen, privacy, cookies, function, content, peroxidation, molecular, gpx, access, glutathione, differ, doicdd, rev, skouta, doijcell, lotze, doi, biochem,

Topics {✒️}

oncogenic-ras-harboring cancer cells p62-keap1-nrf2 pathway protects month download article/chapter iron-dependent cell death acyl-coa synthetase-4 research scholar grant daolin tang declare mitochondrial lipid peroxidation bravo-san pedro jm p53-mediated ferroptotic responses genotype-selective antitumor agents cell signal 28 full article pdf iron-dependent form daolin tang lipid peroxidation molecular life sciences adaptive stress responses privacy choices/manage cookies dixon sj autophagy-related proteins author information authors integrated strategy reveals bone marrow injury animal subjects performed related subjects ros-induced autophagy p53-mediated activity autophagic cell death negative breast cancer check access instant access autophagy promotes ferroptosis pancreatic cancer cells cancer cells assists hepatocellular carcinoma cells cell death subroutines nonapoptotic cell death immunogenic cell death pathobiology rights cancer targets bcl-2 american cancer society regulated cell death p53-mediated ferroptosis article kang angeli jp article log yang ws european economic area maintaining mitochondrial homeostasis

Questions {❓}

  • Autophagy and Ferroptosis—What Is the Connection?
  • Autophagy and Ferroptosis—What Is the Connection?
  • Cox AD, Fesik SW, Kimmelman AC, Luo J, Der CJ (2014) Drugging the undruggable RAS: mission possible?
  • Green DR, Levine B (2014) To be or not to be?

Schema {🗺️}

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         headline:Autophagy and Ferroptosis—What Is the Connection?
         description:Autophagy is a conserved intracellular degradation system and plays a dual role in cell death, depending on context and phase. Ferroptosis is a new form of regulated cell death that mainly depends on iron accumulation and lipid peroxidation. In this review, we summarize the processes of autophagy and ferroptosis and discuss their crosstalk mechanisms at the molecular level. The original study shows that ferroptosis is morphologically, biochemically, and genetically distinct from autophagy and other types of cell death. However, recent studies demonstrate that activation of ferroptosis is indeed dependent on the induction of autophagy. Additionally, many ferroptosis regulators such as SLC7A11, GPX4, NRF2, p53, HSPB1, CISD1, FANCD2, and ACSL4 have been identified as potential regulators of autophagy. This review not only highlights the importance of autophagy as an emerging mechanism of ferroptosis but also raises new insights regarding regulated cell death.
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      headline:Autophagy and Ferroptosis—What Is the Connection?
      description:Autophagy is a conserved intracellular degradation system and plays a dual role in cell death, depending on context and phase. Ferroptosis is a new form of regulated cell death that mainly depends on iron accumulation and lipid peroxidation. In this review, we summarize the processes of autophagy and ferroptosis and discuss their crosstalk mechanisms at the molecular level. The original study shows that ferroptosis is morphologically, biochemically, and genetically distinct from autophagy and other types of cell death. However, recent studies demonstrate that activation of ferroptosis is indeed dependent on the induction of autophagy. Additionally, many ferroptosis regulators such as SLC7A11, GPX4, NRF2, p53, HSPB1, CISD1, FANCD2, and ACSL4 have been identified as potential regulators of autophagy. This review not only highlights the importance of autophagy as an emerging mechanism of ferroptosis but also raises new insights regarding regulated cell death.
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External Links {🔗}(309)

Analytics and Tracking {📊}

  • Google Tag Manager

Libraries {📚}

  • Clipboard.js
  • Prism.js

CDN Services {📦}

  • Crossref

4.88s.