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10.3748/wjg.v21.i47.13259

http://scihub22266oqcxt.onion/10.3748/wjg.v21.i47.13259
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suck abstract from ncbi


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pmid26715808
      World+J+Gastroenterol 2015 ; 21 (47 ): 13259-67
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  • Evaluation of epithelial-mesenchymal transitioned circulating tumor cells in patients with resectable gastric cancer: Relevance to therapy response #MMPMID26715808
  • Li TT ; Liu H ; Li FP ; Hu YF ; Mou TY ; Lin T ; Yu J ; Zheng L ; Li GX
  • World J Gastroenterol 2015[Dec]; 21 (47 ): 13259-67 PMID26715808 show ga
  • AIM: To evaluate the epithelial-to-mesenchymal transition (EMT) of circulating tumor cells (CTCs) in gastric cancer patients. METHODS: We detected tumor cells for expression of four epithelial (E(+)) transcripts (keratins 8, 18, and 19 and epithelial cell adhesion molecule) and two mesenchymal (M(+)) transcripts (Vimentin and Twist) by a quantifiable, dual-colorimetric RNA-in situ hybridization assay. Between July 2014 and October 2014, 44 patients with gastric cancer were recruited for CTC evaluation. Blood samples were obtained from selected patients during the treatment course [before surgery, after surgery and at the 6(th) cycle of XELOX based chemotherapy (about 6 mo postoperatively)]. RESULTS: We found the EMT phenomenon in which there were a few biphenotypic E(+)/M(+) cells in primary human gastric cancer specimens. Of the 44 patients, the presence of CTCs was reported in 35 (79.5%) patients at baseline. Five types of cells including from exclusively E(+) CTCs to intermediate CTCs and exclusively M(+) CTCs were identified (4 patients with M(+) CTCs and 10 patients with M(+) or M(+) > E(+) CTCs). Further, a chemotherapy patient having progressive disease showed a proportional increase of mesenchymal CTCs in the post-treatment blood specimens. We used NCI-N87 cells to analyze the linearity and sensitivity of CanPatrol(TM) system and the correlation coefficient (R(2)) was 0.999. CONCLUSION: The findings suggest that the EMT phenomenon was both in a few cells of primary tumors and abundantly in CTCs from the blood of gastric cancer patients, which might be used to monitor therapy response.
  • |*Epithelial-Mesenchymal Transition [MESH]
  • |*Gastrectomy [MESH]
  • |Adenocarcinoma/blood/genetics/*pathology/*surgery [MESH]
  • |Adult [MESH]
  • |Aged [MESH]
  • |Aged, 80 and over [MESH]
  • |Antineoplastic Combined Chemotherapy Protocols/therapeutic use [MESH]
  • |Biomarkers, Tumor/blood/genetics [MESH]
  • |Capecitabine [MESH]
  • |Case-Control Studies [MESH]
  • |Cell Line, Tumor [MESH]
  • |Chemotherapy, Adjuvant [MESH]
  • |Deoxycytidine/analogs & derivatives/therapeutic use [MESH]
  • |Drug Monitoring/methods [MESH]
  • |Female [MESH]
  • |Fluorouracil/analogs & derivatives/therapeutic use [MESH]
  • |Humans [MESH]
  • |In Situ Hybridization [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Neoplasm Staging [MESH]
  • |Neoplastic Cells, Circulating/metabolism/*pathology [MESH]
  • |Oxaloacetates [MESH]
  • |Phenotype [MESH]
  • |Stomach Neoplasms/blood/genetics/*pathology/*surgery [MESH]
  • |Time Factors [MESH]


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