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<t>Integrinβ1</t> affected CDDP resistance and was regulated by FGL1 in TU212-R cells. A The expression of FGL1 and Integrinβ1 in NP69, TU212 and TU212-R cells was detected by western blot assay. B The cell viability of TU212-R cells was assessed after FGL1 knockdown and treatmentwith Pyrintegrin. C , D Expression levels of FGL1 and Integrinβ1 in TU212-R cellsafter FGL1 knockdown and treatmentwith Pyrintegrin. Grey values were analyzed by Image J software, with expression normalized to GAPDH, n=3.ns indicates no significant difference, ** P < 0.01, *** P < 0.001.
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Effects of cyclic stretching on <t>integrinβ1</t> and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).
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Image Search Results


Integrinβ1 affected CDDP resistance and was regulated by FGL1 in TU212-R cells. A The expression of FGL1 and Integrinβ1 in NP69, TU212 and TU212-R cells was detected by western blot assay. B The cell viability of TU212-R cells was assessed after FGL1 knockdown and treatmentwith Pyrintegrin. C , D Expression levels of FGL1 and Integrinβ1 in TU212-R cellsafter FGL1 knockdown and treatmentwith Pyrintegrin. Grey values were analyzed by Image J software, with expression normalized to GAPDH, n=3.ns indicates no significant difference, ** P < 0.01, *** P < 0.001.

Journal: Discover Oncology

Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro

doi: 10.1007/s12672-025-03337-x

Figure Lengend Snippet: Integrinβ1 affected CDDP resistance and was regulated by FGL1 in TU212-R cells. A The expression of FGL1 and Integrinβ1 in NP69, TU212 and TU212-R cells was detected by western blot assay. B The cell viability of TU212-R cells was assessed after FGL1 knockdown and treatmentwith Pyrintegrin. C , D Expression levels of FGL1 and Integrinβ1 in TU212-R cellsafter FGL1 knockdown and treatmentwith Pyrintegrin. Grey values were analyzed by Image J software, with expression normalized to GAPDH, n=3.ns indicates no significant difference, ** P < 0.01, *** P < 0.001.

Article Snippet: The interaction between Integrinβ1 and Galectin-1 can promote drug resistance of breast cancer cells [ ].

Techniques: Expressing, Western Blot, Knockdown, Software

Downregulation of FGL1 inhibited the migration and invasion abilities of TU212-R cells through regulating Integrinβ1. The migration and invasion abilities of TU212-R cells were determined by wound healing assay (scale bar: 50 μm) (A) and transwell assay (scale bar: 50 μm) (B) after FGL1 knockdown and treatment with Pyrintegrin. n=3, ns means no significant difference, ** P < 0.01, *** P < 0.001.

Journal: Discover Oncology

Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro

doi: 10.1007/s12672-025-03337-x

Figure Lengend Snippet: Downregulation of FGL1 inhibited the migration and invasion abilities of TU212-R cells through regulating Integrinβ1. The migration and invasion abilities of TU212-R cells were determined by wound healing assay (scale bar: 50 μm) (A) and transwell assay (scale bar: 50 μm) (B) after FGL1 knockdown and treatment with Pyrintegrin. n=3, ns means no significant difference, ** P < 0.01, *** P < 0.001.

Article Snippet: The interaction between Integrinβ1 and Galectin-1 can promote drug resistance of breast cancer cells [ ].

Techniques: Migration, Wound Healing Assay, Transwell Assay, Knockdown

Tumorigenicity of TU212-R in vivo. A Representative images of mice bearing TU212-R tumors from different treatment groups. The tumor volume growth curves ( B ) over the study period and the tumor weight ( C ) after injections of different treatment groups. D Immunohistochemical staining for Ki67, FGL1, Integrinβ1 and P-gp proteins in different xenograft tumor tissues (scale bar: 100 μm). The positive area was quantified by Image J software. n = 5, ns means no significant difference, * P < 0.05, ** P < 0.01, *** P < 0.001

Journal: Discover Oncology

Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro

doi: 10.1007/s12672-025-03337-x

Figure Lengend Snippet: Tumorigenicity of TU212-R in vivo. A Representative images of mice bearing TU212-R tumors from different treatment groups. The tumor volume growth curves ( B ) over the study period and the tumor weight ( C ) after injections of different treatment groups. D Immunohistochemical staining for Ki67, FGL1, Integrinβ1 and P-gp proteins in different xenograft tumor tissues (scale bar: 100 μm). The positive area was quantified by Image J software. n = 5, ns means no significant difference, * P < 0.05, ** P < 0.01, *** P < 0.001

Article Snippet: The interaction between Integrinβ1 and Galectin-1 can promote drug resistance of breast cancer cells [ ].

Techniques: In Vivo, Immunohistochemical staining, Staining, Software

The expression of Integrinβ1 and resistance proteins regulated by FGL1 affected apoptosis in vivo. (A) Representative images of TUNEL staining in different xenograft tumor tissues (scale bar: 200 μm). (B) The apoptosis incidence was measured by Image J software. (C) Expression levels of FGL1, Integrinβ1, MRP1 and P-gp in different xenograft tumor tissues were evaluated by western blot assay. n=5, ns indicates no significant difference, * P < 0.05, ** P < 0.01, *** P < 0.001.

Journal: Discover Oncology

Article Title: Effect of fibrinogen like protein 1 on cisplatin-resistance in laryngeal carcinoma through targeting integrinβ1 in vivo and in vitro

doi: 10.1007/s12672-025-03337-x

Figure Lengend Snippet: The expression of Integrinβ1 and resistance proteins regulated by FGL1 affected apoptosis in vivo. (A) Representative images of TUNEL staining in different xenograft tumor tissues (scale bar: 200 μm). (B) The apoptosis incidence was measured by Image J software. (C) Expression levels of FGL1, Integrinβ1, MRP1 and P-gp in different xenograft tumor tissues were evaluated by western blot assay. n=5, ns indicates no significant difference, * P < 0.05, ** P < 0.01, *** P < 0.001.

Article Snippet: The interaction between Integrinβ1 and Galectin-1 can promote drug resistance of breast cancer cells [ ].

Techniques: Expressing, In Vivo, TUNEL Assay, Staining, Software, Western Blot

Effects of cyclic stretching on integrinβ1 and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).

Journal: Micromachines

Article Title: A Microfluidic-Based Cell-Stretching Culture Device That Allows for Easy Preparation of Slides for Observation with High-Magnification Objective Lenses

doi: 10.3390/mi16010093

Figure Lengend Snippet: Effects of cyclic stretching on integrinβ1 and vinculin localization in OP9 cells. Fluorescence images of integrinβ1 (green), f-actin (red), and vinculin (gray) in OP9 cells cultured on the device after 72 h under static conditions followed by 24 h under ( A ) static or ( B ) cyclic stretching conditions (0.5 Hz) photographed with a 100× oil immersion objective lens. Confocal images were captured every 0.48 µm along the z-axis to create z-stacks (14 slices) for maximum-intensity projection (scanning zoom 2×). The right figure shows the fluorescence intensity–distance profiles of integrinβ1 (green), f-actin (red), vinculin (gray), and nuclei (blue) on lines ( a – d ) drawn on the microscope image (MIP).

Article Snippet: For integrinβ1, vinculin, f-actin, and nuclear staining, 0.5% BSA was added with anti-integrinβ1 antibody (0.4 μg/mL; SC-19656, Santa Cruz Biotechnology, Dallas, TX, USA), anti-vinculin antibody (4 μg/mL; 26520-1-AP, Proteintech, Rosemont, IL, USA), and rhodamine phalloidin (1.65 μM; R4159, Thermo Fisher Scientific) and incubated overnight at 4 °C.

Techniques: Fluorescence, Cell Culture, Microscopy

Journal: iScience

Article Title: Exosomal Galectin-3 promotes peritoneal metastases in gastric adenocarcinoma via microenvironment alterations

doi: 10.1016/j.isci.2024.111564

Figure Lengend Snippet:

Article Snippet: Integrinβ1 , Santa Cruz , Cat# sc-8978, RRID: AB_2130101.

Techniques: Microarray, Recombinant, Reverse Transcription, SYBR Green Assay, Enzyme-linked Immunosorbent Assay, Staining, Plasmid Preparation, Bicinchoninic Acid Protein Assay, Software