Sensitive detection of few vital small cell lung cancer (SCLC) cells in blood and sputum by RT-PCR

1995 ◽  
Vol 121 (S1) ◽  
pp. A71-A71
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J. Lacroix ◽  
M. Givenchian ◽  
S. M. Woerner ◽  
P. Drings ◽  
M. von Knebel Doeberitz
Cancers ◽  
2017 ◽  
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David Hout ◽  
Brock Schweitzer ◽  
Kasey Lawrence ◽  
Stephan Morris ◽  
Tracy Tucker ◽  
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Tuncay Goksel ◽  
Berna Komurcuoglu ◽  
Ozge Ozer Kaya ◽  
Berk Ozyilmaz ◽  
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Jonathan Benzaquen ◽  
Audrey Vallee ◽  
Maryline Allegra ◽  
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Cancers ◽  
2019 ◽  
Vol 11 (10) ◽  
pp. 1538 ◽  
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Background: Recent in vitro studies have indicated that irisin inhibits proliferation, migration and epithelial-mesenchymal transition. Irisin expression has not been studied in tumour tissues of non-small cell lung cancer (NSCLC) patients yet. The aim of the study was to determine the irisin expression in NSCLCs in comparison to the clinicopathological factors and expression of TTF-1, p63 and Ki-67. Material and methods: Tissue microarrays with 729 NSCLC and 140 non-malignant lung tissue (NMLT) were used to perform immunohistochemical reactions. Laser Capture Microdissection (LCM) was used to collect cancer and stromal cells from NSCLCs. FNDC5 expression was tested for LCM samples, 75 NSCLCs and 25 NMLTs with the RT-PCR technique. Western-blot, immunofluorescence reaction and RT-PCR assays were performed on lung cancer cell lines. Results: Irisin expression was observed in NSCLC cancer cells and stromal fibroblasts. In cancer cells, irisin expression was decreased in higher grades (G) of malignancy, tumour size (T) and according to lymph node metastasis. In stromal cells, irisin expression was increased in higher G and advanced T. A shorter overall survival was observed in patients with higher irisin expression in NSCLC stromal cells. Conclusions: Irisin expression in stromal fibroblasts may influence cancer cell proliferation and may be a prognostic factor for survival in NSCLC.


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