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      결장직장암과 혈관내피성장인자 발현과의 상관관계 = Expression of Vascular Endothelial Growth Factor in Colorectal Cancer

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      https://www.riss.kr/link?id=A104788700

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      다국어 초록 (Multilingual Abstract)

      Purpose: The neovascularization is an essential factor for
      the growth of solid organ cancer and especially vascular
      endothelial growth factor (VEGF) has been known to the
      very important mediator of neovascularization. Thus, this
      study was searching that expression of VEGF in colorectal
      cancer correlate to clinicopathologic factors. Methods:
      We analyzed 93 patients with sporadic colorectal cancer
      who underwent colectomy and their specimens were
      studied immunohistochemistry at Chosun University
      hospital from March, 2002 to November, 2005. Results:
      The expression rate of VEGF was 61 cases of all (65.6%).
      There were no significant relation VEGF expression to
      age, sex and lymph node metastasis. But, VEGF expression
      in colon cancer was 80.5% rather than 53.8% in rectal
      cancer (P=0.010). Correlation with T staging, expression
      of VEGF was 10.0% in pT0, 62.5% in pT1, pT2 and
      77.2% in pT3, pT4 (P<0.0001), and correlation with
      TNM staging, expression of VEGF was 10.0% in stage
      0, 63.2% in stage I, 72.0% in stage II, 73.3% in stage
      III and 100.0% in stage IV (P=0.001). Conclusions:
      Expression of VEGF in colorectal cancer closely correlates
      with cancer progression and VEGF was more expressed
      in colon cancer than rectum.
      번역하기

      Purpose: The neovascularization is an essential factor for the growth of solid organ cancer and especially vascular endothelial growth factor (VEGF) has been known to the very important mediator of neovascularization. Thus, this study was searching th...

      Purpose: The neovascularization is an essential factor for
      the growth of solid organ cancer and especially vascular
      endothelial growth factor (VEGF) has been known to the
      very important mediator of neovascularization. Thus, this
      study was searching that expression of VEGF in colorectal
      cancer correlate to clinicopathologic factors. Methods:
      We analyzed 93 patients with sporadic colorectal cancer
      who underwent colectomy and their specimens were
      studied immunohistochemistry at Chosun University
      hospital from March, 2002 to November, 2005. Results:
      The expression rate of VEGF was 61 cases of all (65.6%).
      There were no significant relation VEGF expression to
      age, sex and lymph node metastasis. But, VEGF expression
      in colon cancer was 80.5% rather than 53.8% in rectal
      cancer (P=0.010). Correlation with T staging, expression
      of VEGF was 10.0% in pT0, 62.5% in pT1, pT2 and
      77.2% in pT3, pT4 (P<0.0001), and correlation with
      TNM staging, expression of VEGF was 10.0% in stage
      0, 63.2% in stage I, 72.0% in stage II, 73.3% in stage
      III and 100.0% in stage IV (P=0.001). Conclusions:
      Expression of VEGF in colorectal cancer closely correlates
      with cancer progression and VEGF was more expressed
      in colon cancer than rectum.

      더보기

      다국어 초록 (Multilingual Abstract)

      Purpose: The neovascularization is an essential factor for
      the growth of solid organ cancer and especially vascular
      endothelial growth factor (VEGF) has been known to the
      very important mediator of neovascularization. Thus, this
      study was searching that expression of VEGF in colorectal
      cancer correlate to clinicopathologic factors. Methods:
      We analyzed 93 patients with sporadic colorectal cancer
      who underwent colectomy and their specimens were
      studied immunohistochemistry at Chosun University
      hospital from March, 2002 to November, 2005. Results:
      The expression rate of VEGF was 61 cases of all (65.6%).
      There were no significant relation VEGF expression to
      age, sex and lymph node metastasis. But, VEGF expression
      in colon cancer was 80.5% rather than 53.8% in rectal
      cancer (P=0.010). Correlation with T staging, expression
      of VEGF was 10.0% in pT0, 62.5% in pT1, pT2 and
      77.2% in pT3, pT4 (P<0.0001), and correlation with
      TNM staging, expression of VEGF was 10.0% in stage
      0, 63.2% in stage I, 72.0% in stage II, 73.3% in stage
      III and 100.0% in stage IV (P=0.001). Conclusions:
      Expression of VEGF in colorectal cancer closely correlates
      with cancer progression and VEGF was more expressed
      in colon cancer than rectum.
      번역하기

      Purpose: The neovascularization is an essential factor for the growth of solid organ cancer and especially vascular endothelial growth factor (VEGF) has been known to the very important mediator of neovascularization. Thus, this study was searchin...

      Purpose: The neovascularization is an essential factor for
      the growth of solid organ cancer and especially vascular
      endothelial growth factor (VEGF) has been known to the
      very important mediator of neovascularization. Thus, this
      study was searching that expression of VEGF in colorectal
      cancer correlate to clinicopathologic factors. Methods:
      We analyzed 93 patients with sporadic colorectal cancer
      who underwent colectomy and their specimens were
      studied immunohistochemistry at Chosun University
      hospital from March, 2002 to November, 2005. Results:
      The expression rate of VEGF was 61 cases of all (65.6%).
      There were no significant relation VEGF expression to
      age, sex and lymph node metastasis. But, VEGF expression
      in colon cancer was 80.5% rather than 53.8% in rectal
      cancer (P=0.010). Correlation with T staging, expression
      of VEGF was 10.0% in pT0, 62.5% in pT1, pT2 and
      77.2% in pT3, pT4 (P<0.0001), and correlation with
      TNM staging, expression of VEGF was 10.0% in stage
      0, 63.2% in stage I, 72.0% in stage II, 73.3% in stage
      III and 100.0% in stage IV (P=0.001). Conclusions:
      Expression of VEGF in colorectal cancer closely correlates
      with cancer progression and VEGF was more expressed
      in colon cancer than rectum.

      더보기

      참고문헌 (Reference)

      1 Leung DW, "Vascular. endothelial growth factor is a secreted angiogenic mitogen" 246 : 1306-1309, 1989

      2 Dvorak HF, "Vascular permeability factor/vascular endothelial growth factor: A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy" 20 : 4368-4380, 2002

      3 Paley PJ, "Vascular endothelial growth factor expression in early stage ovarian carcinoma" 80 : 98-106, 1997

      4 Masood R, "Vascular endothelial growth factor (VEGF) is an autocrine growth factor for VEGF receptor-positive human tumors" 98 : 1904-1913, 2001

      5 Osella-Abate S, "VEGF-165 serum levels and tyrosinase expression in melanoma patients: correlation with the clinical course" 12 : 325-334, 2002

      6 Senger DR, "Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid" 219 : 983-985, 1983

      7 Folkman J, "Tumor angiogenesis" 43 : 175-203, 1985

      8 Houck KA, "The vascular endothelial growth factor family: Identification of a fourth molecular species and characterization of alternative splicing of RNA" 5 : 1806-1814, 1991

      9 Compton CC, "The staging of colorectal cancer: 2004 and beyond" 54 : 295-308, 2004

      10 Kim TH, "The significance of the lymphatic micro vessel density and vascular endothelial growth factor- C expression for colorectal cancer" 73 : 406-411, 2007

      1 Leung DW, "Vascular. endothelial growth factor is a secreted angiogenic mitogen" 246 : 1306-1309, 1989

      2 Dvorak HF, "Vascular permeability factor/vascular endothelial growth factor: A critical cytokine in tumor angiogenesis and a potential target for diagnosis and therapy" 20 : 4368-4380, 2002

      3 Paley PJ, "Vascular endothelial growth factor expression in early stage ovarian carcinoma" 80 : 98-106, 1997

      4 Masood R, "Vascular endothelial growth factor (VEGF) is an autocrine growth factor for VEGF receptor-positive human tumors" 98 : 1904-1913, 2001

      5 Osella-Abate S, "VEGF-165 serum levels and tyrosinase expression in melanoma patients: correlation with the clinical course" 12 : 325-334, 2002

      6 Senger DR, "Tumor cells secrete a vascular permeability factor that promotes accumulation of ascites fluid" 219 : 983-985, 1983

      7 Folkman J, "Tumor angiogenesis" 43 : 175-203, 1985

      8 Houck KA, "The vascular endothelial growth factor family: Identification of a fourth molecular species and characterization of alternative splicing of RNA" 5 : 1806-1814, 1991

      9 Compton CC, "The staging of colorectal cancer: 2004 and beyond" 54 : 295-308, 2004

      10 Kim TH, "The significance of the lymphatic micro vessel density and vascular endothelial growth factor- C expression for colorectal cancer" 73 : 406-411, 2007

      11 Ferrara N, "The biology of vascular endothelial growth factor" 18 : 4-25, 1997

      12 Ferrara N, "The biology of VEGF and its receptors" 9 : 669-676, 2003

      13 Hicklin DJ, "Role of the vascular endothelial growth factor pathway in tumor growth and angiogenesis" 23 : 1011-1027, 2005

      14 Lee JC, "Prognostic value of vascular endothelial growth factor expression in colorectal cancer patients" 36 : 748-753, 2000

      15 Griffiths L, "Platelet-derived endothelial cell growth factor thymidine phosphorylase in tumour growth and response to therapy" 76 : 689-693, 1997

      16 Jain RK, "Normalization of tumor vasculature: an emerging concept in antiangiogenic therapy" 307 : 58-62, 2005

      17 Bergers G, "Modes of resistance to antiangiogenic therapy-targeted therapy" 8 : 592-603, 2008

      18 Ministry of Health and Welfare, "Korean Cancer Research 2003" Ministry of Health and Welfare 2003

      19 Chen CH, "Fibroblast growth factor 2: from laboratory evidence to clinical application" 2 : 33-43, 2004

      20 Schneider BP, "Drug insight: VEGF as a therapeutic target for breast cancer" 4 : 181-189, 2007

      21 Mise M, "Clinical significance of vascular endothelial growth factor and basic fibroblast growth factor gene expression in liver tumor" 23 : 455-464, 1996

      22 August DA, "Clinical perspective of human colorectal cancer metastasis" 3 : 303-324, 1984

      23 Hurwitz H, "Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer" 350 : 2335-2342, 2004

      24 Hurwitz H, "Bevacizumab plus irinotecan, fluorouracil, and leucovorin for metastatic colorectal cancer" 350 : 2335-2342, 2004

      25 Vincenzi B, "Angiogenesis modifications related with cetuximab plus irinotecan as anticancer treatment in advanced colorectal cancer patients" 17 : 835-841, 2006

      26 Hertig AT, "Angiogenesis in the early human chorion and in the primary placenta of the Macaque monkey" 25 : 37-81, 1935

      27 Giatromanolaki A, "Angiogenesis in colorectal cancer: prognostic and therapeutic implications" 29 : 408-417, 2006

      28 Xiangming C, "Angiogenesis as an unfavorable factor related to lymph node metastasis in early gastric cancer" 5 : 585-589, 1998

      29 Kabbinavar FF, "Addition of bevacizumab to bolus fluorouracil and leucovorin in first-line metastatic colorectal cancer: results of a randomized phase II trial" 23 : 3697-3705, 2005

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2013-03-13 학술지명변경 한글명 : Journal of the Korean Society of Coloproctolgy -> Annals of Coloproctolgy
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      2010-11-26 학술지명변경 한글명 : 대한대장항문학회지 -> Journal of the Korean Society of Coloproctolgy KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2006-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2005-05-30 학술지등록 한글명 : 대한대장항문학회지
      외국어명 : 미등록
      KCI등재후보
      2005-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.09 0.09 0.08
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.07 0.06 0.312 0
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