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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/s13045-022-01365-6.

Title:
The emerging role of pyroptosis in pediatric cancers: from mechanism to therapy | Journal of Hematology & Oncology
Description:
Pediatric cancers are the driving cause of death for children and adolescents. Due to safety requirements and considerations, treatment strategies and drugs for pediatric cancers have been so far scarcely studied. It is well known that tumor cells tend to progressively evade cell death pathways, which is known as apoptosis resistance, one of the hallmarks of cancer, dominating tumor drug resistance. Recently, treatments targeting nonapoptotic cell death have drawn great attention. Pyroptosis, a newly specialized form of cell death, acts as a critical physiological regulator in inflammatory reaction, cell development, tissue homeostasis and stress response. The action in different forms of pyroptosis is of great significance in the therapy of pediatric cancers. Pyroptosis could be induced and consequently modulate tumorigenesis, progression, and metastasis if treated with local or systemic therapies. However, excessive or uncontrolled cell death might lead to tissue damage, acute inflammation, or even cytokine release syndrome, which facilitates tumor progression or recurrence. Herein, we aimed to describe the molecular mechanisms of pyroptosis, to highlight and discuss the challenges and opportunities for activating pyroptosis pathways through various oncologic therapies in multiple pediatric neoplasms, including osteosarcoma, neuroblastoma, leukemia, lymphoma, and brain tumors.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Science
  • Education
  • Health & Fitness

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 5,000,019 visitors per month in the current month.
However, some sources were not loaded, we suggest to reload the page to get complete results.

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

We can't figure out the monetization strategy.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

pubmed, pyroptosis, article, google, scholar, cell, cas, cells, cancer, central, death, caspase, apoptosis, tumor, pediatric, treatment, zhang, wang, osteosarcoma, pathway, cancers, activation, inflammasome, gsdme, nlrp, therapy, expression, drugs, liu, induce, protein, release, oncol, role, gasdermin, mechanisms, neuroblastoma, gsdmd, human, chen, pathways, therapies, lymphoma, membrane, cleavage, leukemia, patients, immune, nat, immunol,

Topics {✒️}

mir-181/sirt1/pgc-1α/nrf2 signaling pathway sirt1/pgc-1α/nrf2 pathway mir-142a-3p enhances flaa c-jun n-terminal kinase irak1/nf-kappab signaling pathway p53/p21/cyclin b1 pathway named n-bm-mscs-exo dpp8/dpp9 inhibitor-induced pyroptosis induce g2/m-phase arrest inducing g2/m-phase arrest el-deiry ws article download pdf multi-anti-tumor pharmacological effects calcium-sensing receptor regulates hypoxic bm-mscs-exo nonselective dpp-inhibitor val-boropro meg3/nlrp3/caspase-1/gsdmd pathway bone marrow-derived macrophages h-bm-mscs-exo assist chemotherapy-induced icd chemotherapy-induced cell death double-strand dna break copper-induced cell death central nervous system nlrp3-mediated il-1β activation oncology small-molecule drugs severe methotrexate-induced toxicity noncanonical pyroptotic pathway pediatric high-grade glioma radiation fosters dose-dependent recurrent/refractory cns tumors chemotherapy drug-induced pyroptosis n-terminal gasdermin domain higher-risk myelodysplastic syndrome including caspase-3/8-mediated pathway trigger mitochondria-mediated apoptosis radiation-mediated intestinal injury potent anti-tumor effect synergistic anti-tumor effect ras-mapk pathway [117] gsdme-dependent cell death calcium-influx-dependent histamine [132] nf-κb signaling pathways death-inducing signaling complex triple-negative breast cancer gram-negative bacterial infections cytokine release syndrome chemotherapy-induced tissue damage dhodh-mediated ferroptosis defence central south university

Questions {❓}

  • Lighting a fire: can we harness pyroptosis to ignite antitumor immunity?
  • Neoadjuvant treatment for resectable and borderline resectable pancreatic cancer: Chemotherapy or chemoradiotherapy?
  • Osteosarcoma treatment—Where do we stand?
  • What’s new in bone forming tumours of the skeleton?

Schema {🗺️}

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         headline:The emerging role of pyroptosis in pediatric cancers: from mechanism to therapy
         description:Pediatric cancers are the driving cause of death for children and adolescents. Due to safety requirements and considerations, treatment strategies and drugs for pediatric cancers have been so far scarcely studied. It is well known that tumor cells tend to progressively evade cell death pathways, which is known as apoptosis resistance, one of the hallmarks of cancer, dominating tumor drug resistance. Recently, treatments targeting nonapoptotic cell death have drawn great attention. Pyroptosis, a newly specialized form of cell death, acts as a critical physiological regulator in inflammatory reaction, cell development, tissue homeostasis and stress response. The action in different forms of pyroptosis is of great significance in the therapy of pediatric cancers. Pyroptosis could be induced and consequently modulate tumorigenesis, progression, and metastasis if treated with local or systemic therapies. However, excessive or uncontrolled cell death might lead to tissue damage, acute inflammation, or even cytokine release syndrome, which facilitates tumor progression or recurrence. Herein, we aimed to describe the molecular mechanisms of pyroptosis, to highlight and discuss the challenges and opportunities for activating pyroptosis pathways through various oncologic therapies in multiple pediatric neoplasms, including osteosarcoma, neuroblastoma, leukemia, lymphoma, and brain tumors.
         datePublished:2022-10-08T00:00:00Z
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            Programmed cell death
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            Osteosarcoma
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            Hematology
            Cancer Research
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      headline:The emerging role of pyroptosis in pediatric cancers: from mechanism to therapy
      description:Pediatric cancers are the driving cause of death for children and adolescents. Due to safety requirements and considerations, treatment strategies and drugs for pediatric cancers have been so far scarcely studied. It is well known that tumor cells tend to progressively evade cell death pathways, which is known as apoptosis resistance, one of the hallmarks of cancer, dominating tumor drug resistance. Recently, treatments targeting nonapoptotic cell death have drawn great attention. Pyroptosis, a newly specialized form of cell death, acts as a critical physiological regulator in inflammatory reaction, cell development, tissue homeostasis and stress response. The action in different forms of pyroptosis is of great significance in the therapy of pediatric cancers. Pyroptosis could be induced and consequently modulate tumorigenesis, progression, and metastasis if treated with local or systemic therapies. However, excessive or uncontrolled cell death might lead to tissue damage, acute inflammation, or even cytokine release syndrome, which facilitates tumor progression or recurrence. Herein, we aimed to describe the molecular mechanisms of pyroptosis, to highlight and discuss the challenges and opportunities for activating pyroptosis pathways through various oncologic therapies in multiple pediatric neoplasms, including osteosarcoma, neuroblastoma, leukemia, lymphoma, and brain tumors.
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         Programmed cell death
         Pediatric cancer
         Osteosarcoma
         Cytokine release syndrome
         Oncology
         Hematology
         Cancer Research
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                     type:PostalAddress
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                  name:The Second Xiangya Hospital of Central South University
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            name:The Second Xiangya Hospital of Central South University
            address:
               name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
               type:PostalAddress
            type:Organization
            name:The Second Xiangya Hospital of Central South University
            address:
               name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China
               type:PostalAddress
            type:Organization
      name:Jieyu He
      affiliation:
            name:The Second Xiangya Hospital of Central South University
            address:
               name:Department of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, China
               type:PostalAddress
            type:Organization
      name:Zhihong Li
      affiliation:
            name:The Second Xiangya Hospital of Central South University
            address:
               name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
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            name:The Second Xiangya Hospital of Central South University
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               type:PostalAddress
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      name:Chao Tu
      affiliation:
            name:The Second Xiangya Hospital of Central South University
            address:
               name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
               type:PostalAddress
            type:Organization
            name:The Second Xiangya Hospital of Central South University
            address:
               name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Xiangya School of Medicine, Central South University, Changsha, China
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Xiangya School of Medicine, Central South University, Changsha, China
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Xiangya School of Medicine, Central South University, Changsha, China
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Department of Geriatrics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Department of Orthopaedics, The Second Xiangya Hospital of Central South University, Changsha, China
      name:Hunan Key Laboratory of Tumor Models and Individualized Medicine, The Second Xiangya Hospital of Central South University, Changsha, China

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