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We are analyzing https://link.springer.com/article/10.1007/s00432-011-0998-9.

Title:
Elevated expression of USP22 in correlation with poor prognosis in patients with invasive breast cancer | Journal of Cancer Research and Clinical Oncology
Description:
Ubiquitin-specific protease 22 (USP22), a novel deubiquitinating enzyme, has been associated with metastasis, therapy resistance, and cell-cycle progression. The purpose of this study was to investigate the expression level of USP22 in breast samples and to evaluate its clinical significance in breast cancer patients. Immunohistochemistry was used to determine the expression of USP22 protein in 31 breast fibroadenoma and 100 breast cancer patients in comparison with 34 normal breast specimens. Furthermore, we analyzed the correlation between the expression of the USP22 protein and various clinicopathologic factors including survival status of patients with breast cancer. The immunohistochemistry results showed that the expression level of USP22 protein in breast cancer samples was significantly higher than that in breast fibroadenoma and normal breast tissues (P = 0.003 and P = 0.021). Moreover, statistical analysis showed that high USP22 expression was positively related to lymph node metastasis, Her-2, Ki67, and recurrence. Furthermore, it was shown that patients with high USP22 expression had significantly poorer outcome compared with patients with low expression of USP22 for patients with positive lymph nodes. Multivariate Cox regression analysis revealed that USP22 expression level was an independent prognostic factor for both overall survival and disease-free survival (P = 0.039 and P = 0.041, respectively). Overexpression of USP22 may contribute to the progression of breast cancer and thus may serve as a new molecular marker to predict the prognosis of breast cancer patients.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Health & Fitness
  • Science

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.
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How Does Link.springer.com Make Money? {💸}

We're unsure how the site profits.

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 {🔍}

article, cancer, google, scholar, pubmed, cas, breast, usp, cell, expression, zhang, patients, analysis, histone, prognosis, metastasis, protein, mol, privacy, cookies, content, journal, research, access, gene, cycle, harbin, information, publish, search, yao, pang, lymph, complex, genes, biol, department, function, data, log, clinical, correlation, poor, june, youxue, lei, protease, deubiquitinating, therapy, progression,

Topics {✒️}

month download article/chapter myc/max/mad network myc-dependent trrap recruitment lymph node metastasis lihong wang & da pang triple-negative breast cancer differentially expressed proteins prognostic markers independent prognostic factor histone h2b ubiquitination ubiquitin-specific protease 14 full article pdf invasive breast cancer positive lymph nodes privacy choices/manage cookies stem cell contribution clinical oncology aims cyclin d2 promoter discrete functional module h2b ubiquitylation acts dr yanlong liu metastasis-enabling phenotype apoptosis-related genes breast cancer samples saga-related complex histone deacetylase inhibitors normal breast tissues cancerous breast tissue c-myc global cancer statistics bladder cancer cells da pang article zhang immunohistochemistry results showed breast cancer patients european economic area disease-free survival chorionic villi derived epigenetic events underlie polycomb-catalyzed ubiquitylation coactivates nuclear receptors counteracts heterochromatin silencing excellent technical assistance microarray analysis identifies conditions privacy policy article journal activated polycomb group cell-cycle progression statistical analysis showed harbin medical university

Schema {🗺️}

WebPage:
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         headline:Elevated expression of USP22 in correlation with poor prognosis in patients with invasive breast cancer
         description:Ubiquitin-specific protease 22 (USP22), a novel deubiquitinating enzyme, has been associated with metastasis, therapy resistance, and cell-cycle progression. The purpose of this study was to investigate the expression level of USP22 in breast samples and to evaluate its clinical significance in breast cancer patients. Immunohistochemistry was used to determine the expression of USP22 protein in 31 breast fibroadenoma and 100 breast cancer patients in comparison with 34 normal breast specimens. Furthermore, we analyzed the correlation between the expression of the USP22 protein and various clinicopathologic factors including survival status of patients with breast cancer. The immunohistochemistry results showed that the expression level of USP22 protein in breast cancer samples was significantly higher than that in breast fibroadenoma and normal breast tissues (P = 0.003 and P = 0.021). Moreover, statistical analysis showed that high USP22 expression was positively related to lymph node metastasis, Her-2, Ki67, and recurrence. Furthermore, it was shown that patients with high USP22 expression had significantly poorer outcome compared with patients with low expression of USP22 for patients with positive lymph nodes. Multivariate Cox regression analysis revealed that USP22 expression level was an independent prognostic factor for both overall survival and disease-free survival (P = 0.039 and P = 0.041, respectively). Overexpression of USP22 may contribute to the progression of breast cancer and thus may serve as a new molecular marker to predict the prognosis of breast cancer patients.
         datePublished:2011-06-21T00:00:00Z
         dateModified:2011-06-21T00:00:00Z
         pageStart:1245
         pageEnd:1253
         sameAs:https://doi.org/10.1007/s00432-011-0998-9
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            Breast cancer
            USP22
            Immunohistochemistry
            Prognosis
            Oncology
            Cancer Research
            Internal Medicine
            Hematology
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      headline:Elevated expression of USP22 in correlation with poor prognosis in patients with invasive breast cancer
      description:Ubiquitin-specific protease 22 (USP22), a novel deubiquitinating enzyme, has been associated with metastasis, therapy resistance, and cell-cycle progression. The purpose of this study was to investigate the expression level of USP22 in breast samples and to evaluate its clinical significance in breast cancer patients. Immunohistochemistry was used to determine the expression of USP22 protein in 31 breast fibroadenoma and 100 breast cancer patients in comparison with 34 normal breast specimens. Furthermore, we analyzed the correlation between the expression of the USP22 protein and various clinicopathologic factors including survival status of patients with breast cancer. The immunohistochemistry results showed that the expression level of USP22 protein in breast cancer samples was significantly higher than that in breast fibroadenoma and normal breast tissues (P = 0.003 and P = 0.021). Moreover, statistical analysis showed that high USP22 expression was positively related to lymph node metastasis, Her-2, Ki67, and recurrence. Furthermore, it was shown that patients with high USP22 expression had significantly poorer outcome compared with patients with low expression of USP22 for patients with positive lymph nodes. Multivariate Cox regression analysis revealed that USP22 expression level was an independent prognostic factor for both overall survival and disease-free survival (P = 0.039 and P = 0.041, respectively). Overexpression of USP22 may contribute to the progression of breast cancer and thus may serve as a new molecular marker to predict the prognosis of breast cancer patients.
      datePublished:2011-06-21T00:00:00Z
      dateModified:2011-06-21T00:00:00Z
      pageStart:1245
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         Breast cancer
         USP22
         Immunohistochemistry
         Prognosis
         Oncology
         Cancer Research
         Internal Medicine
         Hematology
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                  name:The Third Affiliated Hospital of Harbin Medical University
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                     name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
                     type:PostalAddress
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                     type:PostalAddress
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                  name:Institute of Cancer Prevention and Treatment, Harbin Medical University
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         name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
         type:PostalAddress
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               name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
               type:PostalAddress
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      name:Xianyu Zhang
      affiliation:
            name:The Third Affiliated Hospital of Harbin Medical University
            address:
               name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
               type:PostalAddress
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      name:Hongfei Ji
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            name:Institute of Cancer Prevention and Treatment, Harbin Medical University
            address:
               name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
               type:PostalAddress
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      name:Lihong Wang
      affiliation:
            name:Institute of Cancer Prevention and Treatment, Harbin Medical University
            address:
               name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
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      name:Shanshan Sun
      affiliation:
            name:The Third Affiliated Hospital of Harbin Medical University
            address:
               name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
               type:PostalAddress
            type:Organization
      name:Da Pang
      affiliation:
            name:The Third Affiliated Hospital of Harbin Medical University
            address:
               name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
               type:PostalAddress
            type:Organization
            name:Institute of Cancer Prevention and Treatment, Harbin Medical University
            address:
               name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
               type:PostalAddress
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      email:[email protected]
PostalAddress:
      name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
      name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
      name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
      name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
      name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
      name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
      name:Department of Breast Surgery, The Third Affiliated Hospital of Harbin Medical University, Harbin, China
      name:Institute of Cancer Prevention and Treatment, Harbin Medical University, Harbin, China
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External Links {🔗}(119)

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