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month download article/chapter cd147/cd147-mediated metastasis process hab18g/cd147 promotes invasion fak-pi3k-ca2+ pathways membrane-type serine protease direct epithelial-stromal interaction yang zhang & zhinan chen article digestive diseases anti hab18g/cd147 antibody fibroblast activation protein/seprase matrix metalloproteinase-dependent generation independent prognostic indicators full article pdf related subjects emmprin/basigin/ox47/m6 tumor invasion molecules ec871214 cell lines google scholar privacy choices/manage cookies national key discipline tumor cell surface emmprin-mediated mmp regulation world health forum invasive ductal carcinoma mol biol cell mol cell proteomics human colorectal cancer serous ovarian carcinoma mol cancer res tumor-stroma interaction affect cellular architecture cell surface expression human hepatoma cells clin exp metastasis primary tumor tissues lymph node metastasis esophageal carcinoma human corneal grafts hab18g/cd147 mrna results hab18g/cd147 matrix metalloproteinase synthesis matrix metalloproteinase modulator extracellular matrixmetalloproteinase inducer article zhu european economic area received previous therapy potentially therapeutic target extended genomic rearrangements lactate transporters mct1 corneal wound healing

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         headline:Clinical Impact of HAb18G/CD147 Expression in Esophageal Squamous Cell Carcinoma
         description:HAb18G/CD147 expression has been associated with many tumor invasion molecules, which play important roles in recurrence and poor differentiation of esophageal squamous cell carcinoma (ESCC). However, the clinical implications of HAb18G/CD147 in ESCC are still unclear. In this study, we clarified the clinical significance of HAb18G/CD147 and characterized the association between HAb18G/CD147 and tumor invasion in ESCC cases. Tumor tissues were obtained from 86 ESCC patients who underwent surgical resection between 2002 and 2005. All patients that had received previous therapy were excluded. ESCC tissues were analyzed by IHC using anti HAb18G/CD147 antibody. The expression of HAb18G/CD147 mRNA in esophageal cancer cell lines was analyzed by RT–PCR. HAb18G/CD147 was uniformly expressed in EC109 and EC871214 cell lines, but negatively expressed in EPC2, esophageal normal squamous cell line. HAb18G/CD147 mainly localized to the membrane of tumor cells in 84.9% of ESCC patients (64 out of 86 cases). Furthermore, we also found that higher HAb18G/CD147 expression levels significantly correlated with lymph node metastasis, depth of tumor invasion and differentiation (P < 0.05). But the expression levels of HAb18G/CD147 in lymph node metastatic tissues were almost equal to that in the primary tumor tissues. Furthermore, lymph node metastasis and expression of HAB18G/CD147 were independent prognostic indicators in ESCC. The expression of HAb18G/CD147 might be involved in the progression and survival of ESCC. Therefore, HAb18G/CD147 could be a clinical marker for the poor prognosis in ESCC patients and may also be a potentially therapeutic target to improve the progression of ESCC.
         datePublished:2011-07-26T00:00:00Z
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            Immunohistochemistry
            Survival
            Gastroenterology
            Hepatology
            Oncology
            Transplant Surgery
            Biochemistry
            general
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      headline:Clinical Impact of HAb18G/CD147 Expression in Esophageal Squamous Cell Carcinoma
      description:HAb18G/CD147 expression has been associated with many tumor invasion molecules, which play important roles in recurrence and poor differentiation of esophageal squamous cell carcinoma (ESCC). However, the clinical implications of HAb18G/CD147 in ESCC are still unclear. In this study, we clarified the clinical significance of HAb18G/CD147 and characterized the association between HAb18G/CD147 and tumor invasion in ESCC cases. Tumor tissues were obtained from 86 ESCC patients who underwent surgical resection between 2002 and 2005. All patients that had received previous therapy were excluded. ESCC tissues were analyzed by IHC using anti HAb18G/CD147 antibody. The expression of HAb18G/CD147 mRNA in esophageal cancer cell lines was analyzed by RT–PCR. HAb18G/CD147 was uniformly expressed in EC109 and EC871214 cell lines, but negatively expressed in EPC2, esophageal normal squamous cell line. HAb18G/CD147 mainly localized to the membrane of tumor cells in 84.9% of ESCC patients (64 out of 86 cases). Furthermore, we also found that higher HAb18G/CD147 expression levels significantly correlated with lymph node metastasis, depth of tumor invasion and differentiation (P < 0.05). But the expression levels of HAb18G/CD147 in lymph node metastatic tissues were almost equal to that in the primary tumor tissues. Furthermore, lymph node metastasis and expression of HAB18G/CD147 were independent prognostic indicators in ESCC. The expression of HAb18G/CD147 might be involved in the progression and survival of ESCC. Therefore, HAb18G/CD147 could be a clinical marker for the poor prognosis in ESCC patients and may also be a potentially therapeutic target to improve the progression of ESCC.
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         ESCC
         Immunohistochemistry
         Survival
         Gastroenterology
         Hepatology
         Oncology
         Transplant Surgery
         Biochemistry
         general
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      affiliation:
            name:Fourth Military Medical University
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      name:Xiujuan Han
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            name:Fourth Military Medical University
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      name:Department of Gynecology and Obstetrics, Tangdu Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
      name:State Key Laboratory of Cancer Biology, Cell Engineering Research Centre and Department of Cell Biology, National Key Discipline of Cell Biology, Fourth Military Medical University, Xi’an, People’s Republic of China
      name:State Key Laboratory of Cancer Biology, Cell Engineering Research Centre and Department of Cell Biology, National Key Discipline of Cell Biology, Fourth Military Medical University, Xi’an, People’s Republic of China
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