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GC-derived Exosomal DARS-AS1 promoted angiogenesis in vitro. A The morphology and size of <t>HGC-27-derived</t> exosome (HGC-27-EXO) was observed by a TEM (scale bar: 200 nm). B The size of HGC-27-Exo was measured by NTA. C WB analysis was performed to detect typical exosomal biomarkers (CD63 and CD9) in HGC-27 cell lysates or exosomes. D Representative immunofluorescence images showing the internalization of HGC-27- or MKN-45-derived exosomes (green) (HGC-27-EXO and MKN-45-EXO) by HUVECs. Scale bars = 10 μm. E qRT-PCR analysis of DARS-AS1 expression levels in GES-1, HGC-27 and MKN-45 and their corresponding exosomes. F qRT-PCR detection of DARS-AS1 expression in DARS-AS1 knockdown cells and their corresponding exosomes. G qRT-PCR analysis of the expression of DARS-AS1 in HUVECs treated with DARS-AS1 knockdown HGC-27-EXO and MKN-45-EXO or PBS (control). H – K Tube formation and Transwell migration by HUVECs cultured with PBS, HGC-27-EXO and MKN-45-EXO, and tubes and migration cells were quantified. Scale bars = 100 μm. ns. no significant; ** P < 0.01; *** P < 0.001
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GC-derived Exosomal DARS-AS1 promoted angiogenesis in vitro. A The morphology and size of HGC-27-derived exosome (HGC-27-EXO) was observed by a TEM (scale bar: 200 nm). B The size of HGC-27-Exo was measured by NTA. C WB analysis was performed to detect typical exosomal biomarkers (CD63 and CD9) in HGC-27 cell lysates or exosomes. D Representative immunofluorescence images showing the internalization of HGC-27- or MKN-45-derived exosomes (green) (HGC-27-EXO and MKN-45-EXO) by HUVECs. Scale bars = 10 μm. E qRT-PCR analysis of DARS-AS1 expression levels in GES-1, HGC-27 and MKN-45 and their corresponding exosomes. F qRT-PCR detection of DARS-AS1 expression in DARS-AS1 knockdown cells and their corresponding exosomes. G qRT-PCR analysis of the expression of DARS-AS1 in HUVECs treated with DARS-AS1 knockdown HGC-27-EXO and MKN-45-EXO or PBS (control). H – K Tube formation and Transwell migration by HUVECs cultured with PBS, HGC-27-EXO and MKN-45-EXO, and tubes and migration cells were quantified. Scale bars = 100 μm. ns. no significant; ** P < 0.01; *** P < 0.001

Journal: Journal of Cancer Research and Clinical Oncology

Article Title: The GC-derived exosomal LncRNA DARS-AS1 activates Wnt/β-catenin pathway to drive angiogenesis by regulating miR-605-5p/BCL9

doi: 10.1007/s00432-025-06420-6

Figure Lengend Snippet: GC-derived Exosomal DARS-AS1 promoted angiogenesis in vitro. A The morphology and size of HGC-27-derived exosome (HGC-27-EXO) was observed by a TEM (scale bar: 200 nm). B The size of HGC-27-Exo was measured by NTA. C WB analysis was performed to detect typical exosomal biomarkers (CD63 and CD9) in HGC-27 cell lysates or exosomes. D Representative immunofluorescence images showing the internalization of HGC-27- or MKN-45-derived exosomes (green) (HGC-27-EXO and MKN-45-EXO) by HUVECs. Scale bars = 10 μm. E qRT-PCR analysis of DARS-AS1 expression levels in GES-1, HGC-27 and MKN-45 and their corresponding exosomes. F qRT-PCR detection of DARS-AS1 expression in DARS-AS1 knockdown cells and their corresponding exosomes. G qRT-PCR analysis of the expression of DARS-AS1 in HUVECs treated with DARS-AS1 knockdown HGC-27-EXO and MKN-45-EXO or PBS (control). H – K Tube formation and Transwell migration by HUVECs cultured with PBS, HGC-27-EXO and MKN-45-EXO, and tubes and migration cells were quantified. Scale bars = 100 μm. ns. no significant; ** P < 0.01; *** P < 0.001

Article Snippet: The normal gastric mucosal epithelial cell line (GES-1), along with GC cell lines HGC-27 and MKN-45, as well as HUVECs and HEK293T cells, were procured from GeneChem (Shanghai, China).

Techniques: Derivative Assay, In Vitro, Immunofluorescence, Quantitative RT-PCR, Expressing, Knockdown, Control, Migration, Cell Culture

Exosomal DARS-AS1 silence abrogated GC growth and distant metastasis via the inhibition of angiogenesis in vivo. A – C Tumor growth curve of mice subcutaneously implanted with HGC-27 cells treated with HGC-27-EXO sh−NC or HGC-27-EXO shDARS−AS1#1 . Tumor volume ( A ) and weight ( C ) were measured, and tumor size was shown ( B ). D – E Representative images of the abdominal implantation metastases and histogram analysis. E The number of tumor nodes were measured. F – G Sections of tumor were stained with anti-CD31 antibodies by IHC (scale bars = 100 μm). ** P < 0.01; *** P < 0.001

Journal: Journal of Cancer Research and Clinical Oncology

Article Title: The GC-derived exosomal LncRNA DARS-AS1 activates Wnt/β-catenin pathway to drive angiogenesis by regulating miR-605-5p/BCL9

doi: 10.1007/s00432-025-06420-6

Figure Lengend Snippet: Exosomal DARS-AS1 silence abrogated GC growth and distant metastasis via the inhibition of angiogenesis in vivo. A – C Tumor growth curve of mice subcutaneously implanted with HGC-27 cells treated with HGC-27-EXO sh−NC or HGC-27-EXO shDARS−AS1#1 . Tumor volume ( A ) and weight ( C ) were measured, and tumor size was shown ( B ). D – E Representative images of the abdominal implantation metastases and histogram analysis. E The number of tumor nodes were measured. F – G Sections of tumor were stained with anti-CD31 antibodies by IHC (scale bars = 100 μm). ** P < 0.01; *** P < 0.001

Article Snippet: The normal gastric mucosal epithelial cell line (GES-1), along with GC cell lines HGC-27 and MKN-45, as well as HUVECs and HEK293T cells, were procured from GeneChem (Shanghai, China).

Techniques: Inhibition, In Vivo, Staining