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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/s13045-022-01364-7.

Title:
Immune checkpoint of B7-H3 in cancer: from immunology to clinical immunotherapy | Journal of Hematology & Oncology
Description:
Immunotherapy for cancer is a rapidly developing treatment that modifies the immune system and enhances the antitumor immune response. B7-H3 (CD276), a member of the B7 family that plays an immunoregulatory role in the T cell response, has been highlighted as a novel potential target for cancer immunotherapy. B7-H3 has been shown to play an inhibitory role in T cell activation and proliferation, participate in tumor immune evasion and influence both the immune response and tumor behavior through different signaling pathways. B7-H3 expression has been found to be aberrantly upregulated in many different cancer types, and an association between B7-H3 expression and poor prognosis has been established. Immunotherapy targeting B7-H3 through different approaches has been developing rapidly, and many ongoing clinical trials are exploring the safety and efficacy profiles of these therapies in cancer. In this review, we summarize the emerging research on the function and underlying pathways of B7-H3, the expression and roles of B7-H3 in different cancer types, and the advances in B7-H3-targeted therapy. Considering different tumor microenvironment characteristics and results from preclinical models to clinical practice, the research indicates that B7-H3 is a promising target for future immunotherapy, which might eventually contribute to an improvement in cancer immunotherapy that will benefit patients.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

  • Science
  • Education
  • Health & Fitness

Content Management System {šŸ“}

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 {šŸ“ˆ}

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
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How Does Link.springer.com Make Money? {šŸ’ø}

We can't see how the site brings in money.

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 might have a hidden revenue stream, but it's not something we can detect.

Keywords {šŸ”}

cancer, pubmed, cells, article, google, scholar, cell, cas, expression, tumor, central, immune, zhang, wang, receptor, found, targeting, clinical, patients, tumors, tme, tlt, breast, pathway, liu, role, chen, function, therapy, immunotherapy, carcinoma, promotes, response, proliferation, types, models, human, immunol, res, antitumor, expressed, protein, prostate, oncol, activation, potential, signaling, antibody, target, results,

Topics {āœ’ļø}

sirt1/nf-Īŗb/b7-h3/tnf-α axis anti-b7-h3 antibody-drug conjugate pb-labeled b7-h3-targeting antibody car-t-based b7-h3-targeted therapy b7-h3-specific antibody‒drug conjugates ccl2-ccr2-m2 macrophage axis b7-h3/mvp/mek signaling axis jak2/stat3/slug-dependent signaling pathway decrease mhc-ii-peptide formation b7-h3 tri-specific antibody conjugating b7-h3-targeted antibody anti-b7-h3 antibody mediates b7-h3/kif15/erk axis [133] fut8-mediated aberrant n-glycosylation protein-coupled receptor-mediated signaling b7-h3-mediated pro-tumorigenic interaction t-reg cell-based therapies anti-b7-h3 antibodies eliminated b7-h3 augments anti-apoptosis b7-h3-targeted ultrasound imaging endogenous membrane-bound b7-h3 anti-b7-h3 antibody enoblituzumab tumor-derived gm-csf induces b7-h3-targeting radioimmunotherapy agents jak2/stat3/slug signaling pathway b7-h3-stat3-hk2 axis [64] b7-h3ig fusion protein tnf-α-producing state cell-mediated immunoregulatory axis refractory b7-h3-expressing neoplasms b7-h3-based antitumor therapy jak2/stat3/slug/mmp-2/-9 pathway nunes-xavier ce b7-h3-induced glioma progression b7-h3/mvp/mek pathway [58] b7-h3-mediated chemotherapy resistance effector cd8+t-cell function article download pdf 4-1bb/b7-h3 suppressed tumors tumor-expressed b7-h3 mediates anti-cd3 bispecific antibody pd-1xlag3 bispecific antibody including cd3/b7-h3 bispecific b7-h3-overexpressing mb cells b7-h3 molecule enhancing single-pass transmembrane protein b7-h3 monoclonal antibodies targeting cell-cycle machinery immune receptors b7-h3/cd276 palmar-plantar erythron dysesthesia

Questions {ā“}

  • Are B7-H3 CAR-T cells the future universal treatment for pediatric brain tumors?
  • Cutting edge: immune cells as sources and targets of the IL-10 family members?

Schema {šŸ—ŗļø}

WebPage:
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         headline:Immune checkpoint of B7-H3 in cancer: from immunology to clinical immunotherapy
         description:Immunotherapy for cancer is a rapidly developing treatment that modifies the immune system and enhances the antitumor immune response. B7-H3 (CD276), a member of the B7 family that plays an immunoregulatory role in the T cell response, has been highlighted as a novel potential target for cancer immunotherapy. B7-H3 has been shown to play an inhibitory role in T cell activation and proliferation, participate in tumor immune evasion and influence both the immune response and tumor behavior through different signaling pathways. B7-H3 expression has been found to be aberrantly upregulated in many different cancer types, and an association between B7-H3 expression and poor prognosis has been established. Immunotherapy targeting B7-H3 through different approaches has been developing rapidly, and many ongoing clinical trials are exploring the safety and efficacy profiles of these therapies in cancer. In this review, we summarize the emerging research on the function and underlying pathways of B7-H3, the expression and roles of B7-H3 in different cancer types, and the advances in B7-H3-targeted therapy. Considering different tumor microenvironment characteristics and results from preclinical models to clinical practice, the research indicates that B7-H3 is a promising target for future immunotherapy, which might eventually contribute to an improvement in cancer immunotherapy that will benefit patients.
         datePublished:2022-10-25T00:00:00Z
         dateModified:2022-10-25T00:00:00Z
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            Tumor microenvironment
            Cancer immune checkpoints
            Cancer immunotherapy
            Biomarker
            Oncology
            Hematology
            Cancer Research
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                     name:Chinese Academy of Medical Sciences and Peking Union Medical College
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                        name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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                        name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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ScholarlyArticle:
      headline:Immune checkpoint of B7-H3 in cancer: from immunology to clinical immunotherapy
      description:Immunotherapy for cancer is a rapidly developing treatment that modifies the immune system and enhances the antitumor immune response. B7-H3 (CD276), a member of the B7 family that plays an immunoregulatory role in the T cell response, has been highlighted as a novel potential target for cancer immunotherapy. B7-H3 has been shown to play an inhibitory role in T cell activation and proliferation, participate in tumor immune evasion and influence both the immune response and tumor behavior through different signaling pathways. B7-H3 expression has been found to be aberrantly upregulated in many different cancer types, and an association between B7-H3 expression and poor prognosis has been established. Immunotherapy targeting B7-H3 through different approaches has been developing rapidly, and many ongoing clinical trials are exploring the safety and efficacy profiles of these therapies in cancer. In this review, we summarize the emerging research on the function and underlying pathways of B7-H3, the expression and roles of B7-H3 in different cancer types, and the advances in B7-H3-targeted therapy. Considering different tumor microenvironment characteristics and results from preclinical models to clinical practice, the research indicates that B7-H3 is a promising target for future immunotherapy, which might eventually contribute to an improvement in cancer immunotherapy that will benefit patients.
      datePublished:2022-10-25T00:00:00Z
      dateModified:2022-10-25T00:00:00Z
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      pageEnd:31
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      sameAs:https://doi.org/10.1186/s13045-022-01364-7
      keywords:
         B7-H3
         Tumor microenvironment
         Cancer immune checkpoints
         Cancer immunotherapy
         Biomarker
         Oncology
         Hematology
         Cancer Research
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            type:ImageObject
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            name:Binghao Zhao
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                  address:
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                  name:Chinese Academy of Medical Science and Peking Union Medical College
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            name:Huanzhang Li
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                  name:Chinese Academy of Medical Sciences and Peking Union Medical College
                  address:
                     name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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                  name:Chinese Academy of Medical Science and Peking Union Medical College
                  address:
                     name:State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, People’s Republic of China
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            type:Person
            name:Yu Xia
            affiliation:
                  name:Chinese Academy of Medical Sciences and Peking Union Medical College
                  address:
                     name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
                     type:PostalAddress
                  type:Organization
                  name:Chinese Academy of Medical Science and Peking Union Medical College
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            name:Yaning Wang
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                  name:Chinese Academy of Medical Sciences and Peking Union Medical College
                  address:
                     name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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            type:Person
            name:Tian Qu
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                  name:Chinese Academy of Medical Sciences and Peking Union Medical College
                  address:
                     name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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                  name:Chinese Academy of Medical Sciences and Peking Union Medical College
                  address:
                     name:Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, People’s Republic of China
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