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      KCI등재 SCOPUS SCIE

      Role of Matrix Metalloproteinase (MMP) 2 and MMP-9 in Soft Tissue Sarcoma

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      https://www.riss.kr/link?id=A104598233

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      다국어 초록 (Multilingual Abstract)

      Background: We investigated the expression of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in malignant fibrous histiocytoma (MFH), and determined whether these could be useful as prognostic factors.
      Methods: Among patients treated from 1993 to 2007, 30 cases of MFH were evaluated. Immunohistochemical staining was performed for MMP-2, MMP-9, TIMP-1, and TIMP-2 using paraffin wax-embedded blocks of MFH tissues. Reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot and zymography were performed using fresh tissues obtained from 17 of the 30 cases. The levels of MMP and TIMP expression were compared between the MFH and normal control groups, and between non-metastatic and metastatic MFH groups.
      Results: Expression levels of MMP-2, MMP-9, TIMP-1, and TIMP-2 were higher in the MFH group than the control group by RT-PCR, Western blotting, and zymography. Immunohistochemical staining revealed that MMP-2 and MMP-9 protein expression was higher in the metastatic than in the non-metastatic group. The expression levels of MMP-2 and TIMP-1 were significantly higher in the metastatic than in the non-metastatic group (p < 0.05) by RT-PCR. By Western blot analysis, the expression levels of MMP-2, TIMP-1, and TIMP-2 were higher in the metastatic group (p < 0.05), but MMP-9 showed only a slight increase in the metastatic group compared with the non-metastatic group (p > 0.05). Finally, gelatin zymography analysis showed that the expression levels of the pro- and active forms of MMP-2 were significantly higher in the metastatic group (p < 0.05), but the expression of the pro- and active forms of MMP-9 showed a slight decrease in the metastatic group (p > 0.05).
      Conclusions: These results suggest that MMP-2, MMP-9, TIMP-1, and TIMP-2 may have important roles in the development and progression of MFH, and that the degree of expression of these metalloproteinases and their inhibitors, especially MMP-2, could be useful as prognostic factors related to metastasis in MFH.
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      Background: We investigated the expression of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in malignant fibrous histiocytoma (MFH), and determined whether these could be useful as prognostic factors. Methods: Am...

      Background: We investigated the expression of matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases (TIMPs) in malignant fibrous histiocytoma (MFH), and determined whether these could be useful as prognostic factors.
      Methods: Among patients treated from 1993 to 2007, 30 cases of MFH were evaluated. Immunohistochemical staining was performed for MMP-2, MMP-9, TIMP-1, and TIMP-2 using paraffin wax-embedded blocks of MFH tissues. Reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot and zymography were performed using fresh tissues obtained from 17 of the 30 cases. The levels of MMP and TIMP expression were compared between the MFH and normal control groups, and between non-metastatic and metastatic MFH groups.
      Results: Expression levels of MMP-2, MMP-9, TIMP-1, and TIMP-2 were higher in the MFH group than the control group by RT-PCR, Western blotting, and zymography. Immunohistochemical staining revealed that MMP-2 and MMP-9 protein expression was higher in the metastatic than in the non-metastatic group. The expression levels of MMP-2 and TIMP-1 were significantly higher in the metastatic than in the non-metastatic group (p < 0.05) by RT-PCR. By Western blot analysis, the expression levels of MMP-2, TIMP-1, and TIMP-2 were higher in the metastatic group (p < 0.05), but MMP-9 showed only a slight increase in the metastatic group compared with the non-metastatic group (p > 0.05). Finally, gelatin zymography analysis showed that the expression levels of the pro- and active forms of MMP-2 were significantly higher in the metastatic group (p < 0.05), but the expression of the pro- and active forms of MMP-9 showed a slight decrease in the metastatic group (p > 0.05).
      Conclusions: These results suggest that MMP-2, MMP-9, TIMP-1, and TIMP-2 may have important roles in the development and progression of MFH, and that the degree of expression of these metalloproteinases and their inhibitors, especially MMP-2, could be useful as prognostic factors related to metastasis in MFH.

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      참고문헌 (Reference)

      1 Liu J, "Wild-type p53 inhibits nuclear factor-kappaB-induced matrix metalloproteinase-9promoter activation : implications for soft tissue sarcoma growth and metastasis" 4 (4): 803-810, 2006

      2 Schrohl AS, "Tumor tissue levels of tissue inhibitor of metalloproteinase-1 as a prognostic marker in primary breast cancer" 10 (10): 2289-2298, 2004

      3 Albini A, "Tumor cell invasion inhibited by TIMP-2" 83 (83): 775-779, 1991

      4 Stetler-Stevenson WG, "Tumor cell interactions with the extracellular matrix during invasion and metastasis" 9 : 541-573, 1993

      5 Hsu HC, "Treatment results and prognostic factors in patients with malignant fibrous histiocytoma" 43 (43): 530-535, 2004

      6 Murphy G, "Tissue inhibitors of matrix metalloendopeptidases" 248 : 496-510, 1995

      7 Sato H, "Roles of membrane-type matrix metalloproteinase-1 in tumor invasion and metastasis" 96 (96): 212-217, 2005

      8 Ferrari C, "Role of MMP-9 and its tissue inhibitor TIMP-1 in human osteosarcoma : findings in 42 patients followed for 1-16 years" 75 (75): 487-491, 2004

      9 Le Doussal V, "Prognostic factors for patients with localized primary malignant fibrous histiocytoma : a multicenter study of 216 patients with multivariate analysis" 77 (77): 1823-1830, 1996

      10 Jodele S, "Modifying the soil to affect the seed : role of stromal-derived matrix metalloproteinases in cancer progression" 25 (25): 35-43, 2006

      1 Liu J, "Wild-type p53 inhibits nuclear factor-kappaB-induced matrix metalloproteinase-9promoter activation : implications for soft tissue sarcoma growth and metastasis" 4 (4): 803-810, 2006

      2 Schrohl AS, "Tumor tissue levels of tissue inhibitor of metalloproteinase-1 as a prognostic marker in primary breast cancer" 10 (10): 2289-2298, 2004

      3 Albini A, "Tumor cell invasion inhibited by TIMP-2" 83 (83): 775-779, 1991

      4 Stetler-Stevenson WG, "Tumor cell interactions with the extracellular matrix during invasion and metastasis" 9 : 541-573, 1993

      5 Hsu HC, "Treatment results and prognostic factors in patients with malignant fibrous histiocytoma" 43 (43): 530-535, 2004

      6 Murphy G, "Tissue inhibitors of matrix metalloendopeptidases" 248 : 496-510, 1995

      7 Sato H, "Roles of membrane-type matrix metalloproteinase-1 in tumor invasion and metastasis" 96 (96): 212-217, 2005

      8 Ferrari C, "Role of MMP-9 and its tissue inhibitor TIMP-1 in human osteosarcoma : findings in 42 patients followed for 1-16 years" 75 (75): 487-491, 2004

      9 Le Doussal V, "Prognostic factors for patients with localized primary malignant fibrous histiocytoma : a multicenter study of 216 patients with multivariate analysis" 77 (77): 1823-1830, 1996

      10 Jodele S, "Modifying the soil to affect the seed : role of stromal-derived matrix metalloproteinases in cancer progression" 25 (25): 35-43, 2006

      11 Johansson N, "Matrix metalloproteinases in tumor invasion" 57 (57): 5-15, 2000

      12 Nelson AR, "Matrix metalloproteinases : biologic activity and clinical implications" 18 (18): 1135-1149, 2000

      13 Himelstein BP, "Matrix metalloproteinase-9(MMP-9)expression in childhood osseous osteosarcoma" 31 (31): 471-474, 1998

      14 Roebuck MM, "Matrix metalloproteinase expression is related to angiogenesis and histologic grade in spindle cell soft tissue neoplasms of the extremities" 123 (123): 405-414, 2005

      15 Yoshiji H, "Mammary carcinoma cells over-expressing tissue inhibitor of metalloproteinases-1show enhanced vascular endothelial growth factor expression" 75 (75): 81-87, 1998

      16 Salo JC, "Malignant fibrous histiocytoma of the extremity" 85 (85): 1765-1772, 1999

      17 Peiper M, "Malignant fibrous histiocytoma of the extremities and trunk : an institutional review" 135 (135): 59-66, 2004

      18 Bertoni F, "Malignant fibrous histiocytoma of soft tissue : an analysis of 78 cases located and deeply seated in the extremities" 56 (56): 356-367, 1985

      19 Gibbs JF, "Malignant fibrous histiocytoma : an institutional review" 19 (19): 23-27, 2001

      20 Weiss SW, "Malignant fibrous histiocytoma : an analysis of 200 cases" 41 (41): 2250-2266, 1978

      21 Belal A, "Malignant fibrous histiocytoma : a retrospective study of 109 cases" 25 (25): 16-22, 2002

      22 Enzinger FM, "Malignant fibrous histiocytoma 20 years after Stout" 10 (10): 43-53, 1986

      23 Sternlicht MD, "How matrix metalloproteinases regulate cell behavior" 17 : 463-516, 2001

      24 Maguire PD, "Gelatinase and inhibitor expression in soft tissue sarcomas : lack of correlation with distant metastasis" 59 (59): 139-144, 2000

      25 Scapolan M, "Expression profiles in malignant fibrous histiocytomas : clues for differentiating 'spindle cell' and 'pleomorphic' subtypes" 44 (44): 298-309, 2008

      26 Hurskainen T, "Expression of the tissue metalloproteinase inhibitors TIMP-1 and TIMP-2 in malignant fibrous histiocytomas and dermatofibromas as studied by in situ hybridization and immunohistochemistry" 27 (27): 42-49, 1996

      27 Soini Y, "Expression of 72 kilodalton and 92 kilodalton type IV collagenase in malignant fibrous histiocytomas and dermatofibromas" 69 (69): 305-311, 1993

      28 Koga K, "Emmprin in epithelioid sarcoma : expression in tumor cell membrane and stimulation of MMP-2 production in tumor-associated fibroblasts" 120 (120): 761-768, 2007

      29 Reich R, "Effects of inhibitors of plasminogen activator, serine proteinases, and collagenase IV on the invasion of basement membranes by metastatic cells" 48 (48): 3307-3312, 1988

      30 Holten-Andersen M, "Association between preoperative plasma levels of tissue inhibitor of metalloproteinases 1 and rectal cancer patient survival. a validation study" 40 (40): 64-72, 2004

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.06 0.06 0.07
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
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