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      Clinical Usefulness of Cytokeratin 5/6 as an Immunohistochemical Marker to Predict Prognosis in Triple-negative Breast Cancer

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      https://www.riss.kr/link?id=A60253330

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      다국어 초록 (Multilingual Abstract)

      (PR) and human epidermal growth factor receptor 2. Negative staining for all three markers defines the ‘triple-negative’ phenotype. By adding markers for cytokeratin 5/6 and epidermal growth factor receptor, triple-negative breast cancers can be d...

      (PR) and human epidermal growth factor receptor 2. Negative staining for all three markers defines the ‘triple-negative’ phenotype. By adding markers for cytokeratin 5/6 and epidermal growth factor receptor, triple-negative breast cancers can be divided into ‘basal-like’ and ‘non-basal-like’ subgroups. The aim of this study is to asscess the usefulness of cytokeratin 5/6 as a distinguishable marker in the basal-like subgroup of triple-negative breast cancers.
      Methods : We examined, by immunohistochemistry, the expression of biological markers cytokeratin 5/6 in triple-negative breast cancers. We classified triple-negative breast cancerpatients into two groups as cytokeratin 5/6-positive and cytokeratin 5/6-negative. The clinicopathological features, such as disease free survival (DFS) and overall survival (OS) for patients with cytokeratin 5/6-positive were compared with those of the cytokeratin 5/6-negative patients.
      Results : In the 131 cases of operable triple-negative breast cancer, cytokeratin 5/6-positive group was detected in 15 (11.5%) and cytokeratin 5/6-negative group was detected in 116 (88.5%). Significant correlation was observed between cytokeratin 5/6-positive groupwith tumor size, pathologic lymph-node metastasis and American Joint Committee on Cancer staging (pT, pN and stage, P = 0.001). No association was detected between cytokeratin 5/6-positive cancerand other biological markers. Patients with cytokeratin 5/6-positive showed shorter disease-free survival (P = 0.031) and overall survival (P = 0.018) than patients with cytokeratin 5/6-negative.
      Conclusion : Our results show that cytokeratin 5/6 is important markers that can be used to predict prognosis in triple-negative breast cancer. But, there is a need for larger number of cases, more immunohistochemical markers and gene investigation to observe more accurate disease free survivaland overall survival rate

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      목차 (Table of Contents)

      • Introduction
      • Materials and methods
      • Patients and specimens
      • Histology and immunochemistry
      • Statistical Analysis
      • Introduction
      • Materials and methods
      • Patients and specimens
      • Histology and immunochemistry
      • Statistical Analysis
      • Results
      • Discussion
      • Conclusion
      • Acknowledgement
      • Reference
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      참고문헌 (Reference)

      1 Reis-Filho JS, "Triple negative tumours: a critical review" 52 : 108-118, 2008

      2 Sasa M, "Screening for basal marker expression is necessary for decision of therapeutic strategy for triple-negative breast cancer" 97 : 30-34, 2008

      3 Carey LA, "Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study" 295 : 2492-2502, 2006

      4 Livasy CA, "Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma" 19 : 264-271, 2006

      5 Matos I, "P63, cytokeratin 5, and P-cadherin: three molecular markers to distinguish basal phenotype in breast carcinomas" 447 : 688-694, 2005

      6 Perou CM, "Molecular portraits of human breast tumours" 406 : 747-752, 2000

      7 Vielh P, "Ki67 index and S-phase fraction in human beast carcinomas. Comparison and correlations with prognostic factors" 94 : 681-686, 1990

      8 Palacios J, "Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers" 9 : 3606-3614, 2003

      9 Nielsen TO, "Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma" 10 : 5367-5374, 2004

      10 Foulkes WD, "Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer" 95 : 1482-1485, 2003

      1 Reis-Filho JS, "Triple negative tumours: a critical review" 52 : 108-118, 2008

      2 Sasa M, "Screening for basal marker expression is necessary for decision of therapeutic strategy for triple-negative breast cancer" 97 : 30-34, 2008

      3 Carey LA, "Race, breast cancer subtypes, and survival in the Carolina Breast Cancer Study" 295 : 2492-2502, 2006

      4 Livasy CA, "Phenotypic evaluation of the basal-like subtype of invasive breast carcinoma" 19 : 264-271, 2006

      5 Matos I, "P63, cytokeratin 5, and P-cadherin: three molecular markers to distinguish basal phenotype in breast carcinomas" 447 : 688-694, 2005

      6 Perou CM, "Molecular portraits of human breast tumours" 406 : 747-752, 2000

      7 Vielh P, "Ki67 index and S-phase fraction in human beast carcinomas. Comparison and correlations with prognostic factors" 94 : 681-686, 1990

      8 Palacios J, "Immunohistochemical characteristics defined by tissue microarray of hereditary breast cancer not attributable to BRCA1 or BRCA2 mutations: differences from breast carcinomas arising in BRCA1 and BRCA2 mutation carriers" 9 : 3606-3614, 2003

      9 Nielsen TO, "Immunohistochemical and clinical characterization of the basal-like subtype of invasive breast carcinoma" 10 : 5367-5374, 2004

      10 Foulkes WD, "Germline BRCA1 mutations and a basal epithelial phenotype in breast cancer" 95 : 1482-1485, 2003

      11 Sørlie T, "Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications" 98 : 10869-10874, 2001

      12 van de Rijn M, "Expression of cytokeratins 17 and 5 identifies a group of breast carcinomas with poor clinical outcome" 161 : 1991-1996, 2005

      13 Elledge RM, "Estrogen receptor (ER) andprogesterone receptor (PgR) , by ligand-binding assay compared with ER, PgR, pS2, by immune-histochemistry in predicting response to tamoxifen in metastatic breast cancer: a Southwest Oncology Group Study" 89 (89): 111-117, 2000

      14 Cleator S, "Coombes RC:Triple-negative breast cancer: therapeutic options" 8 : 235-244, 2007

      15 Dawson AE, "Comparative assessment of proliferation and DNA content in breast carcinoma by image analysis and flow cytometry" 136 : 1115-1124, 1990

      16 Xin Zhou, "Clinicopathological Characters of Triple Negative Breast Cancer" 22 (22): 17-20, 2010

      17 Kim MJ, "Clinicopathologic significance of the basal-like subtype of breast cancer: a comparison with hormone receptor and HER2/neu-overexpressing phenotypes" 37 : 1217-1226, 2006

      18 Kobayashi S, "Basal-like subtype of breast cancer: a review of its unique characteristics and their clinical significance" 15 : 153-158, 2008

      19 Cheang MC, "Basal-like breast cancer defined by five biomarkers has superior prognostic value than triple-negative phenotype" 14 : 1368-1376, 2008

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2027 평가예정 재인증평가 신청대상 (재인증)
      2021-01-01 평가 등재학술지 유지 (재인증) KCI등재
      2018-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2017-01-01 평가 등재후보학술지 유지 (계속평가) KCI등재후보
      2015-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.02 0.02 0.03
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.04 0.04 0.21 0
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