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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/10.1186/s40364-020-00230-3.

Title:
Targeting ferroptosis in breast cancer | Biomarker Research
Description:
Ferroptosis is a recently discovered distinct type of regulated cell death caused by the accumulation of lipid-based ROS. Metabolism and expression of specific genes affect the occurrence of ferroptosis, making it a promising therapeutic target to manage cancer. Here, we describe the current status of ferroptosis studies in breast cancer and trace the key regulators of ferroptosis back to previous studies. We also compare ferroptosis to common regulated cell death patterns and discuss the sensitivity to ferroptosis in different subtypes of breast cancer. We propose that viewing ferroptosis-related studies from a historical angle will accelerate the development of ferroptosis-based biomarkers and therapeutic strategies in breast cancer.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Health & Fitness
  • Science
  • Education

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 7,626,432 visitors per month in the current month.

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

We're unsure how the site profits.

Earning money isn't the goal of every website; some are designed to offer support or promote social causes. People have different reasons for creating websites. This might be one such reason. Link.springer.com has a revenue plan, but it's either invisible or we haven't found it.

Keywords {🔍}

cancer, breast, google, scholar, article, ferroptosis, cas, cell, cells, death, iron, ros, expression, apoptosis, lipid, acid, fatty, human, gpx, pufas, pathway, wang, chen, found, res, nrf, induced, acsl, acids, induce, growth, autophagy, role, receptor, zhang, ferritin, levels, biol, yang, protein, activity, studies, increased, induces, peroxidation, genes, intracellular, resistance, necroptosis, liu,

Topics {✒️}

cso-ss-cy7-hex/spion/srfn phorbol-12-myristate-13-acetate-induced protein 1 g6pd/hif-1alpha/notch1 axis ros-mediated rip1/rip3/parp-1 pathways gcn2/eif2α/atf4/chac1 pathway gcn2-eif2α-atf4-chac1 pathway [79] gcn2-eif2α-atf4-chac1 pathway rna-binding protein elavl1/hur �oncogenic-ras-selective lethal” property oncogenic-ras-harboring cancer cells glucose-deficient/glutamine-replete conditions ripk1/ripk3/mlkl/chac1 pathway p62-keap1-nrf2 pathway protects ferritin-rich cd68-positive macrophages gcn2/eif2α/atf4 pathway therapy-resistant mesenchymal-high state oestrogen-related receptor alpha long-chain acyl-coenzyme pi3k/akt/nrf2 signaling pathway gcn2-eif2alpha-atf4 pathway nanoparticle ferritin-bound erastin triple-negative cell lines african-centric s47 variant p62/keap1/nrf2/ho-1 pathway vacuolaor-atpase inhibitor archazolid triple-negative breast cancer pufa-induced cell death dna-binding domain leading vital anti-ferroptotic factor autophagy-mediated cell death article download pdf 3-hydroxy-3-methyl-glutaryl-coenzyme tagging single-nucleotide polymorphisms doxorubicin-induced cell death nutrient/serum-deprived condition ripk1/ripk3/mlkl pathway stimulate hormone-responsive cells ros/ask1/jnk pathway nutrient-deprived cancer cells neutral sphingomyelinase-mediated pathway r-ooh forms r-oo· noncanonical perk-nrf2 signaling surmount therapy-resistant cancer e2-induced transient increase withaferin a-induced apoptosis dha-induced cell death autophagy-dependent cell death fish oil-fed rats dmba-induced mammary carcinogenesis induce cell–cycle arrest

Questions {❓}

  • Does iron have a role in breast cancer?
  • For example, what is the marker of ferroptosis?
  • The crosstalk between autophagy and ferroptosis: what can we learn to target drug resistance in cancer?
  • Unsolved mysteries: How does lipid peroxidation cause ferroptosis?
  • What is ferroptosis?
  • What is the biological marker of ferroptosis similar to caspases in apoptosis?

Schema {🗺️}

WebPage:
      mainEntity:
         headline:Targeting ferroptosis in breast cancer
         description:Ferroptosis is a recently discovered distinct type of regulated cell death caused by the accumulation of lipid-based ROS. Metabolism and expression of specific genes affect the occurrence of ferroptosis, making it a promising therapeutic target to manage cancer. Here, we describe the current status of ferroptosis studies in breast cancer and trace the key regulators of ferroptosis back to previous studies. We also compare ferroptosis to common regulated cell death patterns and discuss the sensitivity to ferroptosis in different subtypes of breast cancer. We propose that viewing ferroptosis-related studies from a historical angle will accelerate the development of ferroptosis-based biomarkers and therapeutic strategies in breast cancer.
         datePublished:2020-11-05T00:00:00Z
         dateModified:2020-11-05T00:00:00Z
         pageStart:1
         pageEnd:27
         license:http://creativecommons.org/publicdomain/zero/1.0/
         sameAs:https://doi.org/10.1186/s40364-020-00230-3
         keywords:
            Ferroptosis
            Breast cancer
            Regulated cell death
            Crosstalk
            Ferroptotic regulators
            Historical perspective
            Biomedicine
            general
            Cancer Research
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                     address:
                        name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
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ScholarlyArticle:
      headline:Targeting ferroptosis in breast cancer
      description:Ferroptosis is a recently discovered distinct type of regulated cell death caused by the accumulation of lipid-based ROS. Metabolism and expression of specific genes affect the occurrence of ferroptosis, making it a promising therapeutic target to manage cancer. Here, we describe the current status of ferroptosis studies in breast cancer and trace the key regulators of ferroptosis back to previous studies. We also compare ferroptosis to common regulated cell death patterns and discuss the sensitivity to ferroptosis in different subtypes of breast cancer. We propose that viewing ferroptosis-related studies from a historical angle will accelerate the development of ferroptosis-based biomarkers and therapeutic strategies in breast cancer.
      datePublished:2020-11-05T00:00:00Z
      dateModified:2020-11-05T00:00:00Z
      pageStart:1
      pageEnd:27
      license:http://creativecommons.org/publicdomain/zero/1.0/
      sameAs:https://doi.org/10.1186/s40364-020-00230-3
      keywords:
         Ferroptosis
         Breast cancer
         Regulated cell death
         Crosstalk
         Ferroptotic regulators
         Historical perspective
         Biomedicine
         general
         Cancer Research
      image:
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      isPartOf:
         name:Biomarker Research
         issn:
            2050-7771
         volumeNumber:8
         type:
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            PublicationVolume
      publisher:
         name:BioMed Central
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Zhaoqing Li
            affiliation:
                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
                  type:Organization
                  name:Zhejiang University
                  address:
                     name:Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China
                     type:PostalAddress
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                  name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province
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                     type:PostalAddress
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            name:Lini Chen
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                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
                  type:Organization
                  name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province
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                     name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province, Hangzhou, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Cong Chen
            affiliation:
                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
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                  name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province
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                     name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province, Hangzhou, China
                     type:PostalAddress
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            name:Yulu Zhou
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                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
                  type:Organization
                  name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province
                  address:
                     name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province, Hangzhou, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Dengdi Hu
            affiliation:
                  name:Cixi People’s Hospital Medical and Health Group
                  address:
                     name:Cixi People’s Hospital Medical and Health Group, Ningbo, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Jingjing Yang
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                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
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                  name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province
                  address:
                     name:Biomedical Research Center and Key Laboratory of Biotherapy of Zhejiang Province, Hangzhou, China
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Yongxia Chen
            affiliation:
                  name:Zhejiang University
                  address:
                     name:Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University, Hangzhou, China
                     type:PostalAddress
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                     name:Cixi People’s Hospital Medical and Health Group, Ningbo, China
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                  address:
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