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      Lethal Giant Larvae2 Expression Is Reduced or Localized at Cytoplasm in Colon Adenomas and Adenocarcinomas

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      https://www.riss.kr/link?id=A101633619

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      다국어 초록 (Multilingual Abstract)

      Background : The Scribble, Par and Crumbs polarity modules are essential for establishing and maintaining apicobasal cell polarity in epithelial cells. The aim of the present study was to investigate the expression pattern of Lethal giant larvae2 (Lgl...

      Background : The Scribble, Par and Crumbs polarity modules are essential for establishing and maintaining apicobasal cell polarity in epithelial cells. The aim of the present study was to investigate the expression pattern of Lethal giant larvae2 (Lgl2) in normal colonic epithelium and epithelial tumors and to examine the relationship between Lgl2 expression and clinicopathological parameters. Methods : We examined Lgl2 expression in 66 primary colon cancers and 20 adenomas by immunohistochemistry. Results : In normal colonic epithelium, Lgl2 was strongly expressed at the basolateral membrane of cells in the luminal surface but was not expressed at the base of crypts. The expression pattern of E-cadherin in normal epithelium was similar to that of Lgl2. In contrast, tumors did not express Lgl2 or showed diffuse cytoplasmic staining. The Lgl2 positive rate in tumors was significantly lower than in normal epithelium, and its negative rate in tumors was higher in tumors with abnormal E-cadherin expression than in tumors with positive membranous staining. Lgl2 staining intensity was significantly lower in tumor budding sites than in tumor centers. No significant differences were observed between Lgl2 and clinicopathological parameters. Conclusions : Lgl2 expression was reduced or localized at the cytoplasm in colon epithelial tumors, suggesting that a perturbation of Lgl2 expression frequently occurs in colon epithelial tumors.

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      참고문헌 (Reference)

      1 Grifoni D, "aPKCzeta cortical loading is associated with Lgl cytoplasmic release and tumor growth in Drosophila and human epithelia" 26 : 5960-5965, 2007

      2 Brabletz T, "Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment" 98 : 10356-10361, 2001

      3 Spaderna S, "The transcriptional repressor ZEB1 promotes metastasis and loss of cell polarity in cancer" 68 : 537-544, 2008

      4 Aigner K, "The transcription factor ZEB1(deltaEF1)promotes tumour cell dedifferentiation by repressing master regulators of epithelial polarity" 26 : 6979-6988, 2007

      5 Gumbiner B, "The role of the cell adhesion molecule uvomorulin in the formation and maintenance of the epithelial junctional complex" 107 : 1575-1587, 1988

      6 Grifoni D, "The human protein Hugl-1 substitutes for Drosophila lethal giant larvae tumour suppressor function in vivo" 23 : 8688-8694, 2004

      7 Tepass U, "Shotgun encodes Drosophila E-cadherin and is preferentially required during cell rearrangement in the neurectoderm and other morphogenetically active epithelia" 10 : 672-685, 1996

      8 Schimanski CC, "Reduced expression of Hugl-1,the human homologue of Drosophila tumour suppressor gene lgl,contributes to progression of colorectal cancer" 24 : 3100-3109, 2005

      9 Assémat E, "Polarity complex proteins" 1778 : 614-630, 2008

      10 Drubin DG, "Origins of cell polarity" 84 : 335-344, 1996

      1 Grifoni D, "aPKCzeta cortical loading is associated with Lgl cytoplasmic release and tumor growth in Drosophila and human epithelia" 26 : 5960-5965, 2007

      2 Brabletz T, "Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment" 98 : 10356-10361, 2001

      3 Spaderna S, "The transcriptional repressor ZEB1 promotes metastasis and loss of cell polarity in cancer" 68 : 537-544, 2008

      4 Aigner K, "The transcription factor ZEB1(deltaEF1)promotes tumour cell dedifferentiation by repressing master regulators of epithelial polarity" 26 : 6979-6988, 2007

      5 Gumbiner B, "The role of the cell adhesion molecule uvomorulin in the formation and maintenance of the epithelial junctional complex" 107 : 1575-1587, 1988

      6 Grifoni D, "The human protein Hugl-1 substitutes for Drosophila lethal giant larvae tumour suppressor function in vivo" 23 : 8688-8694, 2004

      7 Tepass U, "Shotgun encodes Drosophila E-cadherin and is preferentially required during cell rearrangement in the neurectoderm and other morphogenetically active epithelia" 10 : 672-685, 1996

      8 Schimanski CC, "Reduced expression of Hugl-1,the human homologue of Drosophila tumour suppressor gene lgl,contributes to progression of colorectal cancer" 24 : 3100-3109, 2005

      9 Assémat E, "Polarity complex proteins" 1778 : 614-630, 2008

      10 Drubin DG, "Origins of cell polarity" 84 : 335-344, 1996

      11 Banks L, "On the guardians of polarity and the disorientation of cancer" 27 : 6876-6877, 2008

      12 Müsch A, "Mammalian homolog of Drosophila tumor suppressor lethal(2)giant larvae interacts with basolateral exocytic machinery in Madin-Darby canine kidney cells" 13 : 158-168, 2002

      13 Yamanaka T, "Mammalian Lgl forms a protein complex with PAR-6 and aPKC independently of PAR-3 to regulate epithelial cell polarity" 13 : 734-743, 2003

      14 Klezovitch O, "Loss of cell polarity causes severe brain dysplasia in Lgl1 knockout mice" 18 : 559-571, 2004

      15 Yamanaka T, "Lgl mediates apical domain disassembly by suppressing the PAR-3-aPKC-PAR-6 complex to orient apical membrane polarity" 119 : 2107-2118, 2006

      16 Vasioukhin V, "Lethal giant puzzle of Lgl" 28 : 13-24, 2006

      17 Laprise P, "Human homolog of disc-large is required for adherens junction assembly and differentiation of human intestinal epithelial cells" 279 : 10157-0166, 2004

      18 Kuphal S, "Expression of Hugl-1 is strongly reduced in malignant melanoma" 25 : 103-110, 2006

      19 장태정, "Expression of E-cadherin and β-catenin is Altered at Tumor Budding Sites, Whose Number is Associated with the Progression of Colorectal Carcinoma" 대한병리학회 43 (43): 523-527, 2009

      20 Bilder D, "Epithelial polarity and proliferation control:links from the Drosophila neoplastic tumor suppressors" 18 : 1909-1925, 2004

      21 Reuver SM, "E-cadherin mediated cell adhesion recruits SAP97 into the cortical cytoskeleton" 111 (111): 1071-1080, 1998

      22 Rolls MM, "Drosophila aPKC regulates cell polarity and cell proliferation in neuroblasts and epithelia" 163 : 1089-1098, 2003

      23 Albertson R, "Dlg,Scrib and Lgl regulate neuroblast cell size and mitotic spindle asymmetry" 5 : 166-170, 2003

      24 장태정, "Cyclooxygenase-2 Expression Is Related to the Epithelial-to-Mesenchymal Transition in Human Colon Cancers" 연세대학교의과대학 50 (50): 818-824, 2009

      25 Bilder D, "Cooperative regulation of cell polarity and growth by Drosophila tumor suppressors" 289 : 113-116, 2000

      26 Humbert PO, "Control of tumourigenesis by the Scribble/Dlg/Lgl polarity module" 27 : 6888-6907, 2008

      27 Lisovsky M, "Cell polarity protein Lgl2 is lost or aberrantly localized in gastric dysplasia and adenocarcinoma:an immunohistochemical study" 22 : 977-984, 2009

      28 Jeanes A, "Cadherins and cancer:how does cadherin dysfunction promote tumor progression?" 27 : 6920-6929, 2008

      29 Lassmann S, "Array CGH identifies distinct DNA copy number profiles of oncogenes and tumor suppressor genes in chromosomal-and microsatellite-unstable sporadic colorectal carcinomas" 85 : 293-304, 2007

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2014-12-24 학술지명변경 한글명 : The Korean Journal of Pathology -> Journal of Pathology and Translational Medicine
      외국어명 : The Korean Journal of Pathology -> Journal of Pathology and Translational Medicine
      KCI등재
      2010-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-04-13 학술지명변경 한글명 : 대한병리학회지 -> The Korean Journal of Pathology KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.13 0.13 0.12
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.13 0.11 0.409 0.01
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