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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
  8. Questions
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We are analyzing https://link.springer.com/article/10.1186/bcr1983.

Title:
Evaluation of the current knowledge limitations in breast cancer research: a gap analysis | Breast Cancer Research
Description:
Background A gap analysis was conducted to determine which areas of breast cancer research, if targeted by researchers and funding bodies, could produce the greatest impact on patients. Methods Fifty-six Breast Cancer Campaign grant holders and prominent UK breast cancer researchers participated in a gap analysis of current breast cancer research. Before, during and following the meeting, groups in seven key research areas participated in cycles of presentation, literature review and discussion. Summary papers were prepared by each group and collated into this position paper highlighting the research gaps, with recommendations for action. Results Gaps were identified in all seven themes. General barriers to progress were lack of financial and practical resources, and poor collaboration between disciplines. Critical gaps in each theme included: (1) genetics (knowledge of genetic changes, their effects and interactions); (2) initiation of breast cancer (how developmental signalling pathways cause ductal elongation and branching at the cellular level and influence stem cell dynamics, and how their disruption initiates tumour formation); (3) progression of breast cancer (deciphering the intracellular and extracellular regulators of early progression, tumour growth, angiogenesis and metastasis); (4) therapies and targets (understanding who develops advanced disease); (5) disease markers (incorporating intelligent trial design into all studies to ensure new treatments are tested in patient groups stratified using biomarkers); (6) prevention (strategies to prevent oestrogen-receptor negative tumours and the long-term effects of chemoprevention for oestrogen-receptor positive tumours); (7) psychosocial aspects of cancer (the use of appropriate psychosocial interventions, and the personal impact of all stages of the disease among patients from a range of ethnic and demographic backgrounds). Conclusion Through recommendations to address these gaps with future research, the long-term benefits to patients will include: better estimation of risk in families with breast cancer and strategies to reduce risk; better prediction of drug response and patient prognosis; improved tailoring of treatments to patient subgroups and development of new therapeutic approaches; earlier initiation of treatment; more effective use of resources for screening populations; and an enhanced experience for people with or at risk of breast cancer and their families. The challenge to funding bodies and researchers in all disciplines is to focus on these gaps and to drive advances in knowledge into improvements in patient care.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Health & Fitness
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {πŸ“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 7,626,182 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

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The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com has a revenue plan, but it's either invisible or we haven't found it.

Keywords {πŸ”}

cancer, breast, pubmed, article, google, scholar, research, cas, patients, clinical, risk, cells, studies, disease, therapies, analysis, progression, tumour, brca, development, treatment, mammary, women, cell, growth, markers, gap, response, pathways, psychosocial, gene, prevention, models, gaps, signalling, understanding, receptor, study, data, central, trials, therapy, methods, stem, early, table, expression, screening, gland, tissue,

Topics {βœ’οΈ}

adrian harris sex-hormone binding globulin rare moderate-penetrance alleles article download pdf asselin-labat ml pgr-negative tamoxifen-resistant cancers sentinel lymph nodes large genome-wide association node-positive breast cancer professor joyce taylor-papadimitriou post-menopausal breast cancer lox-stop-lox cassette scientific advisory board nrg1/neuregulin 1/heregulin gene high-throughput genomic screening improves anti-hormone response low-penetrance alleles continue computer-aided detection programmes anti-growth factor therapies search collaborators tumour microarray/proteomic profiles lymph node stage long-lived cell lines including anti-growth factors lymph node micrometastases aiding patient decision-making oestrogen-receptor positive tumours high-throughput genomic technology mammographic breast density alternative signal transduction bilateral risk-reducing mastectomy undergone risk-reducing surgery activate brca1-dependent ubiquitylation 2/neu-amplified breast cancer high-resolution dna microarrays her2-positive breast cancer evidence-based expert opinion short-term intervention studies gland-specific cre recombinase intra-operative detection method high-throughput discovery tools subclass-specific markers based include mammographic density author information authors oestrogen receptor alpha breast cancer campaign breast cancer campaign' end-stage breast cancer michael steel increased investigator-driven studies

Questions {❓}

  • Bingham SA, Luben R, Welch A, Wareham N, Khaw KT, Day N: Are imprecise methods obscuring a relation between fat and breast cancer?
  • Exploiting the potential of gene expression profiling: is it ready for the clinic?
  • For example, does attending screening negate women's interest in prevention strategies because many women perceive screening as prevention?
  • How do anti-cancer treatments adversely affect cancer cells?
  • How to decide when to stop treatment?
  • Kamb A: What's wrong with our cancer models?
  • Maurice A, Evans DG, Shenton A, Ashcroft L, Baildam A, Barr L, Byrne G, Bundred N, Boggis C, Wilson M, Duffy SW, Howell A: Screening younger women with a family history of breast cancer – does early detection improve outcome?
  • The key question is: does introducing a new marker change clinical practice and therefore patient outcome?
  • What are the gaps?
  • What are the problems?
  • What do we know?
  • Who will develop drug-resistant tumours?

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Evaluation of the current knowledge limitations in breast cancer research: a gap analysis
         description:A gap analysis was conducted to determine which areas of breast cancer research, if targeted by researchers and funding bodies, could produce the greatest impact on patients. Fifty-six Breast Cancer Campaign grant holders and prominent UK breast cancer researchers participated in a gap analysis of current breast cancer research. Before, during and following the meeting, groups in seven key research areas participated in cycles of presentation, literature review and discussion. Summary papers were prepared by each group and collated into this position paper highlighting the research gaps, with recommendations for action. Gaps were identified in all seven themes. General barriers to progress were lack of financial and practical resources, and poor collaboration between disciplines. Critical gaps in each theme included: (1) genetics (knowledge of genetic changes, their effects and interactions); (2) initiation of breast cancer (how developmental signalling pathways cause ductal elongation and branching at the cellular level and influence stem cell dynamics, and how their disruption initiates tumour formation); (3) progression of breast cancer (deciphering the intracellular and extracellular regulators of early progression, tumour growth, angiogenesis and metastasis); (4) therapies and targets (understanding who develops advanced disease); (5) disease markers (incorporating intelligent trial design into all studies to ensure new treatments are tested in patient groups stratified using biomarkers); (6) prevention (strategies to prevent oestrogen-receptor negative tumours and the long-term effects of chemoprevention for oestrogen-receptor positive tumours); (7) psychosocial aspects of cancer (the use of appropriate psychosocial interventions, and the personal impact of all stages of the disease among patients from a range of ethnic and demographic backgrounds). Through recommendations to address these gaps with future research, the long-term benefits to patients will include: better estimation of risk in families with breast cancer and strategies to reduce risk; better prediction of drug response and patient prognosis; improved tailoring of treatments to patient subgroups and development of new therapeutic approaches; earlier initiation of treatment; more effective use of resources for screening populations; and an enhanced experience for people with or at risk of breast cancer and their families. The challenge to funding bodies and researchers in all disciplines is to focus on these gaps and to drive advances in knowledge into improvements in patient care.
         datePublished:2008-03-27T00:00:00Z
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            Oncology
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      headline:Evaluation of the current knowledge limitations in breast cancer research: a gap analysis
      description:A gap analysis was conducted to determine which areas of breast cancer research, if targeted by researchers and funding bodies, could produce the greatest impact on patients. Fifty-six Breast Cancer Campaign grant holders and prominent UK breast cancer researchers participated in a gap analysis of current breast cancer research. Before, during and following the meeting, groups in seven key research areas participated in cycles of presentation, literature review and discussion. Summary papers were prepared by each group and collated into this position paper highlighting the research gaps, with recommendations for action. Gaps were identified in all seven themes. General barriers to progress were lack of financial and practical resources, and poor collaboration between disciplines. Critical gaps in each theme included: (1) genetics (knowledge of genetic changes, their effects and interactions); (2) initiation of breast cancer (how developmental signalling pathways cause ductal elongation and branching at the cellular level and influence stem cell dynamics, and how their disruption initiates tumour formation); (3) progression of breast cancer (deciphering the intracellular and extracellular regulators of early progression, tumour growth, angiogenesis and metastasis); (4) therapies and targets (understanding who develops advanced disease); (5) disease markers (incorporating intelligent trial design into all studies to ensure new treatments are tested in patient groups stratified using biomarkers); (6) prevention (strategies to prevent oestrogen-receptor negative tumours and the long-term effects of chemoprevention for oestrogen-receptor positive tumours); (7) psychosocial aspects of cancer (the use of appropriate psychosocial interventions, and the personal impact of all stages of the disease among patients from a range of ethnic and demographic backgrounds). Through recommendations to address these gaps with future research, the long-term benefits to patients will include: better estimation of risk in families with breast cancer and strategies to reduce risk; better prediction of drug response and patient prognosis; improved tailoring of treatments to patient subgroups and development of new therapeutic approaches; earlier initiation of treatment; more effective use of resources for screening populations; and an enhanced experience for people with or at risk of breast cancer and their families. The challenge to funding bodies and researchers in all disciplines is to focus on these gaps and to drive advances in knowledge into improvements in patient care.
      datePublished:2008-03-27T00:00:00Z
      dateModified:2008-03-27T00:00:00Z
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      pageEnd:25
      license:http://creativecommons.org/licenses/by/2.0/
      sameAs:https://doi.org/10.1186/bcr1983
      keywords:
         Breast Cancer
         Sentinel Lymph Node
         Mammographic Density
         Breast Screening
         Breast Cancer Research
         Cancer Research
         Oncology
         Surgical Oncology
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                  address:
                     name:Department of Surgery and Molecular Oncology, University of Dundee, Dundee, UK
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:Keith Brennan
            affiliation:
                  name:University of Manchester
                  address:
                     name:Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK
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                     name:Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
                     type:PostalAddress
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                  address:
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                     type:PostalAddress
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                  address:
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                     type:PostalAddress
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                     type:PostalAddress
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      name:Nightingale & Genesis Prevention Centre, Wythenshawe Hospital
      address:
         name:Family History Clinic, Nightingale & Genesis Prevention Centre, Wythenshawe Hospital, Manchester, UK
         type:PostalAddress
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      address:
         name:Academic Unit of Clinical Oncology, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK
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      address:
         name:Breast Cancer Prevention Centre, South Manchester University Hospitals NHS Trust, Manchester, UK
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         type:PostalAddress
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         type:PostalAddress
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      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Alastair Thompson
      affiliation:
            name:University of Dundee
            address:
               name:Department of Surgery and Molecular Oncology, University of Dundee, Dundee, UK
               type:PostalAddress
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      email:[email protected]
      name:Keith Brennan
      affiliation:
            name:University of Manchester
            address:
               name:Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK
               type:PostalAddress
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      name:Angela Cox
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            name:University of Sheffield Medical School
            address:
               name:Institute for Cancer Studies, University of Sheffield Medical School, Sheffield, UK
               type:PostalAddress
            type:Organization
      name:Julia Gee
      affiliation:
            name:Cardiff University
            address:
               name:Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:Diana Harcourt
      affiliation:
            name:School of Psychology University of the West of England
            address:
               name:The Centre for Appearance Research, School of Psychology University of the West of England, Bristol, UK
               type:PostalAddress
            type:Organization
      name:Adrian Harris
      affiliation:
            name:John Radcliffe Hospital, University of Oxford
            address:
               name:Cancer Research UK Molecular Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Headington, UK
               type:PostalAddress
            type:Organization
      name:Michelle Harvie
      affiliation:
            name:Nightingale & Genesis Prevention Centre, Wythenshawe Hospital
            address:
               name:Family History Clinic, Nightingale & Genesis Prevention Centre, Wythenshawe Hospital, Manchester, UK
               type:PostalAddress
            type:Organization
      name:Ingunn Holen
      affiliation:
            name:University of Sheffield
            address:
               name:Academic Unit of Clinical Oncology, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK
               type:PostalAddress
            type:Organization
      name:Anthony Howell
      affiliation:
            name:South Manchester University Hospitals NHS Trust
            address:
               name:Breast Cancer Prevention Centre, South Manchester University Hospitals NHS Trust, Manchester, UK
               type:PostalAddress
            type:Organization
      name:Robert Nicholson
      affiliation:
            name:Cardiff University
            address:
               name:Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
               type:PostalAddress
            type:Organization
      name:Michael Steel
      affiliation:
            name:University of St Andrews, Bute Medical School, University of St Andrews
            address:
               name:University of St Andrews, Bute Medical School, University of St Andrews, Fife, UK
               type:PostalAddress
            type:Organization
      name:Charles Streuli
      affiliation:
            name:University of Manchester
            address:
               name:Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Surgery and Molecular Oncology, University of Dundee, Dundee, UK
      name:Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK
      name:Institute for Cancer Studies, University of Sheffield Medical School, Sheffield, UK
      name:Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
      name:The Centre for Appearance Research, School of Psychology University of the West of England, Bristol, UK
      name:Cancer Research UK Molecular Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Headington, UK
      name:Family History Clinic, Nightingale & Genesis Prevention Centre, Wythenshawe Hospital, Manchester, UK
      name:Academic Unit of Clinical Oncology, School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK
      name:Breast Cancer Prevention Centre, South Manchester University Hospitals NHS Trust, Manchester, UK
      name:Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
      name:University of St Andrews, Bute Medical School, University of St Andrews, Fife, UK
      name:Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, UK

External Links {πŸ”—}(386)

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