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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
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We are analyzing https://link.springer.com/article/10.1007/s10555-009-9198-3.

Title:
Phosphatidylinositol 3-kinase (PI3K) pathway activation in bladder cancer | Cancer and Metastasis Reviews
Description:
The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {šŸ“š}

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

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

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Keywords {šŸ”}

cancer, google, scholar, pathway, pubmed, article, cas, bladder, mutations, pten, tsc, mutation, tumours, cell, pik, akt, tumour, expression, protein, activation, kinase, gene, journal, human, pikca, ras, found, inhibitors, development, research, mtor, complex, alterations, carcinoma, knowles, molecular, identified, genes, fig, erbb, invasive, signalling, studies, activity, tuberous, sclerosis, oncogene, cancers, urothelial, clinical,

Topics {āœ’ļø}

growth-factor signalling adenovirus-delivered cre recombinase epidermal growth factor birt-hogg-dubƩ syndrome birt-hogg-dube syndrome article download pdf regulates mtor signaling growth factor withdrawal bladder carcinogen butyl-n receptor tyrosine kinases muscle-invasive urothelial carcinoma pkbalpha/akt1 acts downstream muscle-invasive bladder cancer class ia p110 um-uc3 cell lines deliver wild-type akt1 tsc1-null urothelial cells erk-mediated negative regulation human lkb1/stk11 gene uk/genetics/cgp/cosmic/ high-grade papillary tumours tumor suppressor loci c-erbb-2 gene product constitutive downstream signalling gtpase-activating protein complex control mtor signaling combined pi3k-mtor inhibition akt signaling pathway targeting pi3k signalling dual pi3k-mtor inhibitors low-grade papillary tumours individual tumour-specific information open access privacy choices/manage cookies bmc research notes transitional cell carcinoma transitional-cell carcinoma regulates mtor activity bmc medical genetic tumour suppressor loci array-based cgh analysis increased cell size individualised targeted therapy metastasis reviews aims rieger-christ tumour-suppressor gene pi3k pathway-targeted agents urothelial cell carcinoma dominant negative akt nature reviews cancer

Questions {ā“}

  • Molecular subtypes of bladder cancer: Jekyll and Hyde or chalk and cheese?

Schema {šŸ—ŗļø}

WebPage:
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         headline:Phosphatidylinositol 3-kinase (PI3K) pathway activation in bladder cancer
         description:The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.
         datePublished:2009-12-16T00:00:00Z
         dateModified:2009-12-16T00:00:00Z
         pageStart:305
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            TSC1
            Cancer Research
            Oncology
            Biomedicine
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      headline:Phosphatidylinositol 3-kinase (PI3K) pathway activation in bladder cancer
      description:The phosphatidylinositol 3-kinase (PI3K) pathway is a critical signal transduction pathway that regulates multiple cellular functions. Aberrant activation of this pathway has been identified in a wide range of cancers. Several pathway components including AKT, PI3K and mTOR represent potential therapeutic targets and many small molecule inhibitors are in development or early clinical trials. The complex regulation of the pathway, together with the multiple mechanisms by which it can be activated, make this a highly challenging pathway to target. For successful inhibition, detailed molecular information on individual tumours will be required and it is already clear that different tumour types show distinct combinations of alterations. Recent results have identified alterations in pathway components PIK3CA, PTEN, AKT1 and TSC1 in bladder cancer, some of which are significantly related to tumour phenotype and clinical behaviour. Co-existence of alterations to several PI3K pathway genes in some bladder tumours indicates that these proteins may have functions that are not related solely to the known canonical pathway.
      datePublished:2009-12-16T00:00:00Z
      dateModified:2009-12-16T00:00:00Z
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      name:Cancer Research UK Clinical Centre, Leeds Institute of Molecular Medicine, St James’s University Hospital, Leeds, UK
      name:Cancer Research UK Clinical Centre, Leeds Institute of Molecular Medicine, St James’s University Hospital, Leeds, UK

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