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LINK . SPRINGER . COM {}

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  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
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We are analyzing https://link.springer.com/article/10.1007/s00259-025-07123-3.

Title:
Exploring the landscape of current in vitro and in vivo models and their relevance for targeted radionuclide theranostics | European Journal of Nuclear Medicine and Molecular Imaging
Description:
Cancer remains a leading cause of mortality globally, driving ongoing research into innovative treatment strategies. Preclinical research forms the base for developing these novel treatments, using both in vitro and in vivo model systems that are, ideally, as clinically representative as possible. Emerging as a promising approach for cancer management, targeted radionuclide theranostics (TRT) uses radiotracers to deliver (cytotoxic) radionuclides specifically to cancer cells. Since the field is relatively new, more advanced preclinical models are not yet regularly applied in TRT research. This narrative review examines the currently applied in vitro, ex vivo and in vivo models for oncological research, discusses if and how these models are now applied for TRT studies, and whether not yet applied models can be of benefit for the field. A selection of different models is discussed, ranging from in vitro two-dimensional (2D) and three-dimensional (3D) cell models, including spheroids, organoids and tissue slice cultures, to in vivo mouse cancer models, such as cellline-derived models, patient-derived xenograft models and humanized models. Each of the models has advantages and limitations for studying human cancer biology, radiopharmaceutical assessment and treatment efficacy. Overall, there is a need to apply more advanced models in TRT research that better address specific TRT phenomena, such as crossfire and abscopal effects, to enhance the clinical relevance and effectiveness of preclinical TRT evaluations.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Science
  • Education
  • Health & Fitness

Content Management System {๐Ÿ“}

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 {๐Ÿ“ˆ}

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

๐ŸŒ  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.

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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

We're unsure if the website is profiting.

Not all websites focus on profit; some are designed to educate, connect people, or share useful tools. People create websites for numerous reasons. And this could be one such example. Link.springer.com could have a money-making trick up its sleeve, but it's undetectable for now.

Keywords {๐Ÿ”}

models, cell, cancer, pubmed, article, google, scholar, cas, cells, tumour, model, therapy, research, studies, mice, central, tumours, imaging, trt, mouse, vivo, spheroids, lines, culture, human, vitro, targeted, radiotracers, response, cultures, humanized, radionuclide, preclinical, organoids, radiotracer, study, immune, tissue, effects, expression, therapeutic, uptake, med, including, compared, tme, treatment, development, effect, microfluidic,

Topics {โœ’๏ธ}

gov/news-events/press-announcements/fda-approves grpr-targeted radiotracer [177lu]lu-dota-sp714 grpr-targeting radiotracer [177lu]lu-dota-sp714 pd-1-targeted radiotracer [89zr]zr-antiโ€“hpd-1 p53-mediated radiosensitization of177lu-dotatate higher [177lu]lu-dota-sp714 targeting radiotracer [177lu]lu-eb-rgd patient-specific single-domain antibodies lutetium-177-labeled psma-specific tracers prostate-specific membrane antigen targeted radiotracer [68ga]ga-psma-11 article download pdf [89zr]zr-antiโ€“hpd-1 gastrin-releasing peptide receptor egg test-chorioallantoic membrane anti-hpd-l1 tumour uptake patient-derived xenograft models conventional/nanomaterial-based theranostics evaluation gov/drugsatfda_docs/appletter/2016/208547orig1s000ltr gov/drugsatfda_docs/appletter/2018/208700orig1s000ltr gov/drugsatfda_docs/appletter/2022/215833orig1s000ltr patient-derived xenograft cryopreservation 2 mbq [177lu]lu-psma genetically-modified cell lines double-strand dna breaks including [68ga]ga-dotatate modifying epithelial-mesenchymal transition anti-idiotypic radionuclide therapy cell line-derived tumours patient-derived cell model [177lu]lu-psma-617 performed pd-l1 microspect/ct imaging carbon-ion beam irradiation psma-binding ligand212pb-ng001 chick chorioallantoic membrane targeted ฮฑ-particle therapy nras-mutant melanoma models continuous long-term culture patient-derived cancer organoids [68ga]nodaga-rgdyk uptake abnormal protein localisation/accumulation vivo nras-mutated melanoma tissue-derived primary cells [177lu]lu-psma [177lu]lu-psma-617 patient-derived tumour tissues pd-1-expressing t-cells patient-derived meningioma spheroids genetic/molecular tumour profiles chorioallantoic membrane model

Questions {โ“}

  • Can current preclinical strategies for radiopharmaceutical development meet the needs of targeted alpha therapy?
  • In vitro methodologies to evaluate nanocarriers for cancer treatment: where are we?
  • What is the role of the bystander response in radionuclide therapies?

Schema {๐Ÿ—บ๏ธ}

WebPage:
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         headline:Exploring the landscape of current in vitro and in vivo models and their relevance for targeted radionuclide theranostics
         description:Cancer remains a leading cause of mortality globally, driving ongoing research into innovative treatment strategies. Preclinical research forms the base for developing these novel treatments, using both in vitro and in vivo model systems that are, ideally, as clinically representative as possible. Emerging as a promising approach for cancer management, targeted radionuclide theranostics (TRT) uses radiotracers to deliver (cytotoxic) radionuclides specifically to cancer cells. Since the field is relatively new, more advanced preclinical models are not yet regularly applied in TRT research. This narrative review examines the currently applied in vitro, ex vivo and in vivo models for oncological research, discusses if and how these models are now applied for TRT studies, and whether not yet applied models can be of benefit for the field. A selection of different models is discussed, ranging from in vitro two-dimensional (2D) and three-dimensional (3D) cell models, including spheroids, organoids and tissue slice cultures, to in vivo mouse cancer models, such as cellline-derived models, patient-derived xenograft models and humanized models. Each of the models has advantages and limitations for studying human cancer biology, radiopharmaceutical assessment and treatment efficacy. Overall, there is a need to apply more advanced models in TRT research that better address specific TRT phenomena, such as crossfire and abscopal effects, to enhance the clinical relevance and effectiveness of preclinical TRT evaluations.
         datePublished:2025-02-28T00:00:00Z
         dateModified:2025-02-28T00:00:00Z
         pageStart:3291
         pageEnd:3311
         license:http://creativecommons.org/licenses/by/4.0/
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            In vivo models
            Preclinical research
            Cancer
            Nuclear Medicine
            Imaging / Radiology
            Orthopedics
            Cardiology
            Oncology
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      headline:Exploring the landscape of current in vitro and in vivo models and their relevance for targeted radionuclide theranostics
      description:Cancer remains a leading cause of mortality globally, driving ongoing research into innovative treatment strategies. Preclinical research forms the base for developing these novel treatments, using both in vitro and in vivo model systems that are, ideally, as clinically representative as possible. Emerging as a promising approach for cancer management, targeted radionuclide theranostics (TRT) uses radiotracers to deliver (cytotoxic) radionuclides specifically to cancer cells. Since the field is relatively new, more advanced preclinical models are not yet regularly applied in TRT research. This narrative review examines the currently applied in vitro, ex vivo and in vivo models for oncological research, discusses if and how these models are now applied for TRT studies, and whether not yet applied models can be of benefit for the field. A selection of different models is discussed, ranging from in vitro two-dimensional (2D) and three-dimensional (3D) cell models, including spheroids, organoids and tissue slice cultures, to in vivo mouse cancer models, such as cellline-derived models, patient-derived xenograft models and humanized models. Each of the models has advantages and limitations for studying human cancer biology, radiopharmaceutical assessment and treatment efficacy. Overall, there is a need to apply more advanced models in TRT research that better address specific TRT phenomena, such as crossfire and abscopal effects, to enhance the clinical relevance and effectiveness of preclinical TRT evaluations.
      datePublished:2025-02-28T00:00:00Z
      dateModified:2025-02-28T00:00:00Z
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         In vitro models
         In vivo models
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         Cancer
         Nuclear Medicine
         Imaging / Radiology
         Orthopedics
         Cardiology
         Oncology
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               name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
      name:Joana D. Campeiro
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      affiliation:
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            address:
               name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
      name:Simone U. Dalm
      url:http://orcid.org/0000-0002-6393-6901
      affiliation:
            name:Erasmus MC
            address:
               name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
               type:PostalAddress
            type:Organization
      email:[email protected]
PostalAddress:
      name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
      name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands
      name:Department of Radiology and Nuclear Medicine, Erasmus MC, Rotterdam, The Netherlands

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