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      KCI등재 SCOPUS SCIE

      Epigenetic inactivation of RUNX3 in colorectal cancer

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      https://www.riss.kr/link?id=A105049079

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      다국어 초록 (Multilingual Abstract)

      Purpose: The purpose of this study was to evaluate the efficacy of Betafoam in terms of wound healing and safety. Methods: Fifty-four male adult Sprague-Dawley rats (weight, 200–250 g) were used in the study. Full-thickness skin defects were crea...

      Purpose: The purpose of this study was to evaluate the efficacy of Betafoam in terms of wound healing and safety.
      Methods: Fifty-four male adult Sprague-Dawley rats (weight, 200–250 g) were used in the study. Full-thickness skin defects were created on the back of each rats. The rats were assigned to 6 groups according to the type of wound dressing used (n = 9 for each group): Betafoam, Allevyn-Ag, Mepilex-Ag, Medifoam silver, Polymem-Ag, and gauze. The wound size, histological findings, and amount of DNA on the changed dressings for each group were analyzed and compared.
      Results: All groups showed an effective decrease in wound size. However, the differences between Betafoam and the other dressings were statistically significant on day 14 (P < 0.05). The number of newly generated blood vessels in the Betafoam group was significantly higher than in the gauze, Allevyn-Ag, and Medifoam silver groups (P < 0.001). In the Betafoam group, the proportion of collagen deposition was highest and showed a significantly superior arrangement of collagen fibers compared with the gauze, Allevyn-Ag, Mepilex-Ag, and Medifoam silver groups. The total content of the remaining DNA counts of the exchanged dressings were significantly lower in the Betafoam group than the others.
      Conclusion: Betafoam is effective in wound healing and provides the best performance amongst the various types of dressing materials in terms of re-epithelialization, angiogenesis, collagen deposition, and tissue invasion.

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      목차 (Table of Contents)

      • INTRODUCTION
      • METHODS
      • RESULTS
      • DISCUSSION
      • REFERENCES
      • INTRODUCTION
      • METHODS
      • RESULTS
      • DISCUSSION
      • REFERENCES
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      참고문헌 (Reference)

      1 Guo C, "Tumor suppressor gene Runx3 sensitizes gastric cancer cells to chemotherapeutic drugs by downregulating Bcl-2, MDR-1 and MRP-1" 116 : 155-160, 2005

      2 Bae SC, "Tumor suppressor activity of RUNX3" 23 : 4336-4340, 2004

      3 Li QL, "Transcriptional silencing of the RUNX3 gene by CpG hypermethylation is associated with lung cancer" 314 : 223-228, 2004

      4 Soong R, "The expression of RUNX3 in colorectal cancer is associated with disease stage and patient outcome" 100 : 676-679, 2009

      5 Levanon D, "Runx3 knockouts and stomach cancer" 4 : 560-564, 2003

      6 Chi XZ, "RUNX3 suppresses gastric epithelial cell growth by inducing p21(WAF1/Cip1) expression in cooperation with transforming growth factor {beta}-activated SMAD" 25 : 8097-8107, 2005

      7 Nishio M, "RUNX3 promoter methylation in colorectal cancer: its relationship with microsatellite instability and its suitability as a novel serum tumor marker" 30 : 2673-2682, 2010

      8 Torquati A, "RUNX3 inhibits cell proliferation and induces apoptosis by reinstating transforming growth factor beta responsiveness in esophageal adenocarcinoma cells" 136 : 310-316, 2004

      9 Ito Y, "RUNX transcription factors as key targets of TGF-beta superfamily signaling" 13 : 43-47, 2003

      10 Ozaki T, "RUNX family participates in the regulation of p53-dependent DNA damage response" 2013 : 271347-, 2013

      1 Guo C, "Tumor suppressor gene Runx3 sensitizes gastric cancer cells to chemotherapeutic drugs by downregulating Bcl-2, MDR-1 and MRP-1" 116 : 155-160, 2005

      2 Bae SC, "Tumor suppressor activity of RUNX3" 23 : 4336-4340, 2004

      3 Li QL, "Transcriptional silencing of the RUNX3 gene by CpG hypermethylation is associated with lung cancer" 314 : 223-228, 2004

      4 Soong R, "The expression of RUNX3 in colorectal cancer is associated with disease stage and patient outcome" 100 : 676-679, 2009

      5 Levanon D, "Runx3 knockouts and stomach cancer" 4 : 560-564, 2003

      6 Chi XZ, "RUNX3 suppresses gastric epithelial cell growth by inducing p21(WAF1/Cip1) expression in cooperation with transforming growth factor {beta}-activated SMAD" 25 : 8097-8107, 2005

      7 Nishio M, "RUNX3 promoter methylation in colorectal cancer: its relationship with microsatellite instability and its suitability as a novel serum tumor marker" 30 : 2673-2682, 2010

      8 Torquati A, "RUNX3 inhibits cell proliferation and induces apoptosis by reinstating transforming growth factor beta responsiveness in esophageal adenocarcinoma cells" 136 : 310-316, 2004

      9 Ito Y, "RUNX transcription factors as key targets of TGF-beta superfamily signaling" 13 : 43-47, 2003

      10 Ozaki T, "RUNX family participates in the regulation of p53-dependent DNA damage response" 2013 : 271347-, 2013

      11 Ku JL, "Promoter hypermethylation downregulates RUNX3 gene expression in colorectal cancer cell lines" 23 : 6736-6742, 2004

      12 Kato N, "Hypermethylation of the RUNX3 gene promoter in testicular yolk sac tumor of infants" 163 : 387-391, 2003

      13 박원상, "Hypermethylation of the RUNX3 gene in hepatocellular carcinoma" 생화학분자생물학회 37 (37): 276-281, 2005

      14 Xiao WH, "Hemizygous deletion and hypermethylation of RUNX3 gene in hepatocellular carcinoma" 10 : 376-380, 2004

      15 Nakase Y, "Frequent loss of RUNX3 gene expression in remnant stomach cancer and adjacent mucosa with special reference to topography" 92 : 562-569, 2005

      16 Oshimo Y, "Frequent loss of RUNX3 expression by promoter hypermethylation in gastric carcinoma" 71 : 137-143, 2004

      17 Osaki M, "Expression of RUNX3 protein in human gastric mucosa, intestinal metaplasia and carcinoma" 34 : 605-612, 2004

      18 Lao VV, "Epigenetics and colorectal cancer" 8 : 686-700, 2011

      19 Goel A, "Epigenetic inactivation of RUNX3 in microsatellite unstable sporadic colon cancers" 112 : 754-759, 2004

      20 Fukushige S, "DNA methylation in cancer: a gene silencing mechanism and the clinical potential of its biomarkers" 229 : 173-185, 2013

      21 Ogino S, "CpG island methylation, response to combination chemotherapy, and patient survival in advanced microsatellite stable colorectal carcinoma" 450 : 529-537, 2007

      22 Mu WP, "Clinical significance and association of RUNX3 hypermethylation frequency with colorectal cancer: a meta-analysis" 7 : 1237-1245, 2014

      23 Li QL, "Causal relationship between the loss of RUNX3 expression and gastric cancer" 109 : 113-124, 2002

      24 Siegel R, "Cancer statistics, 2014" 64 : 9-29, 2014

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-11-12 학술지명변경 한글명 : 대한외과학회지 -> Annals of Surgical Treatment and Research KCI등재
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-12-30 학술지명변경 외국어명 : Journal of The Korean Surgical Society -> Annals of Surgical Treatment and Research KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2005-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2004-01-01 평가 등재후보학술지 유지 (등재후보1차) KCI등재후보
      2002-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.39 0.21 0.97
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.73 0.56 0.328 0.06
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