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ATCC cell cultures human oscc cell lines cal27

Figure 1. Effect of DMF on <t>CAL27,</t> HSC-2 and HSC-3 cell viability. DMF treatment at the concen- trations of 500 µM was able to signiﬁcantly reduce cell viability by 41% on CAL27 cells (A), 43% on HSC-2 (B) cells and 46% on HSC-3 cells (C). DMF 1 mM was able to reduce cell viability by 31% on CAL27 cells, 34% on HSC-2 cells and 33% on HSC-3 cells. DMF 10 mM reduced cell viability by 21% on CAL27 cells, 23% on HSC-2 cells and 24% on HSC-3 cells.

Cell Cultures Human Oscc Cell Lines Cal27, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1949 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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1) Product Images from "Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition."

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

Journal: International journal of molecular sciences

doi: 10.3390/ijms24032777

Figure 1. Effect of DMF on CAL27, HSC-2 and HSC-3 cell viability. DMF treatment at the concen- trations of 500 µM was able to signiﬁcantly reduce cell viability by 41% on CAL27 cells (A), 43% on HSC-2 (B) cells and 46% on HSC-3 cells (C). DMF 1 mM was able to reduce cell viability by 31% on CAL27 cells, 34% on HSC-2 cells and 33% on HSC-3 cells. DMF 10 mM reduced cell viability by 21% on CAL27 cells, 23% on HSC-2 cells and 24% on HSC-3 cells.

Figure Legend Snippet: Figure 1. Effect of DMF on CAL27, HSC-2 and HSC-3 cell viability. DMF treatment at the concen- trations of 500 µM was able to signiﬁcantly reduce cell viability by 41% on CAL27 cells (A), 43% on HSC-2 (B) cells and 46% on HSC-3 cells (C). DMF 1 mM was able to reduce cell viability by 31% on CAL27 cells, 34% on HSC-2 cells and 33% on HSC-3 cells. DMF 10 mM reduced cell viability by 21% on CAL27 cells, 23% on HSC-2 cells and 24% on HSC-3 cells.

Techniques Used:

Figure 2. Effect of DMF on HO-1 and MnSOD expression in CAL27 cells. The blots revealed a signiﬁcant increase of HO-1 expression following DMF treatment at the concentration of 1 mM and 10 mM (A). DMF at the same doses was also able to signiﬁcant increase the expression of MnSOD (B). (A,B) * p < 0.05 vs. CAL27; ** p < 0.01 vs. CAL27; *** p < 0.001 vs. CAL27.

Figure Legend Snippet: Figure 2. Effect of DMF on HO-1 and MnSOD expression in CAL27 cells. The blots revealed a signiﬁcant increase of HO-1 expression following DMF treatment at the concentration of 1 mM and 10 mM (A). DMF at the same doses was also able to signiﬁcant increase the expression of MnSOD (B). (A,B) * p < 0.05 vs. CAL27; ** p < 0.01 vs. CAL27; *** p < 0.001 vs. CAL27.

Techniques Used: Expressing, Concentration Assay

Figure 5. Effect of DMF on CAL27 migration. The wound healing assay (scratch test) revealed a signiﬁcant reduction in the number of cells migrating to the scratched area, following 48 h of DMF treatment at the concentration of 1 mM and 10 mM. ** p < 0.01 vs. CAL27.

Figure Legend Snippet: Figure 5. Effect of DMF on CAL27 migration. The wound healing assay (scratch test) revealed a signiﬁcant reduction in the number of cells migrating to the scratched area, following 48 h of DMF treatment at the concentration of 1 mM and 10 mM. ** p < 0.01 vs. CAL27.

Techniques Used: Migration, Wound Healing Assay, Concentration Assay

Figure 7. Effect of DMF on tumor growth in CAL27 orthotopic model. DMF treatment at doses of 30 and 100 mg/kg was able to signiﬁcantly reduce submucosa tumor mass of the tongue and neutrophilic inﬁltration compared to control group (A). No important weight differences were detected between animals (B). Data are representative of at least three independent experiments. Sections were observed and photographed at 10× magniﬁcation. *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC; ### p < 0.001 vs. OSCC.

Figure Legend Snippet: Figure 7. Effect of DMF on tumor growth in CAL27 orthotopic model. DMF treatment at doses of 30 and 100 mg/kg was able to signiﬁcantly reduce submucosa tumor mass of the tongue and neutrophilic inﬁltration compared to control group (A). No important weight differences were detected between animals (B). Data are representative of at least three independent experiments. Sections were observed and photographed at 10× magniﬁcation. *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC; ### p < 0.001 vs. OSCC.

Techniques Used: Control

Figure 8. Effect of DMF on Caspase3, BAD and BCL-2 expression in tongue samples (A–C). The blots revealed an increase of pro-apoptotic BAD expression after DMF treatment especially at the dose of 100 mg/kg and Caspase 3 at both doses. A decrease of anti-apoptotic BCL-2 expression followed DMF treatment in a dose dependent manner compared to OSCC group. Data are representative of at least three independent experiments. (A,B) ## p < 0.01 vs. OSCC; (C) *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC.

Figure Legend Snippet: Figure 8. Effect of DMF on Caspase3, BAD and BCL-2 expression in tongue samples (A–C). The blots revealed an increase of pro-apoptotic BAD expression after DMF treatment especially at the dose of 100 mg/kg and Caspase 3 at both doses. A decrease of anti-apoptotic BCL-2 expression followed DMF treatment in a dose dependent manner compared to OSCC group. Data are representative of at least three independent experiments. (A,B) ## p < 0.01 vs. OSCC; (C) *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC.

Techniques Used: Expressing

Figure 9. Effect of DMF on HO-1 and MnSOD expression in tongue samples (A,B). The blots revealed a signiﬁcant increase of antioxidant expression of HO-1 after DMF treatment especially at the dose of 100 mg/kg and MnSOD at both doses. (A) * p < 0.05 vs. SHAM; ## p < 0.01 vs. OSCC; (B) ** p < 0.01 vs. SHAM; # p < 0.05 vs. OSCC.

Figure Legend Snippet: Figure 9. Effect of DMF on HO-1 and MnSOD expression in tongue samples (A,B). The blots revealed a signiﬁcant increase of antioxidant expression of HO-1 after DMF treatment especially at the dose of 100 mg/kg and MnSOD at both doses. (A) * p < 0.05 vs. SHAM; ## p < 0.01 vs. OSCC; (B) ** p < 0.01 vs. SHAM; # p < 0.05 vs. OSCC.

Techniques Used: Expressing

Expressing:

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.
Article Snippet: 4.1.2.. Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).. CAL27 cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM) (Life Technologies, Gibco®; Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS, Life Technologies, Gibco®; Carlsbad, CA, USA), 100 U/mL of penicillin and 100 μg/mL of streptomycin.CAL27 cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM) (Life Technologies, Gibco®; Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS, Life Technologies, Gibco®; Carlsbad, CA, USA), 100 U/mL of penicillin and 100 μg/mL of streptomycin.

Concentration Assay:

Migration:

Wound Healing Assay:

Control:

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Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 1. Effect of DMF on CAL27, HSC-2 and HSC-3 cell viability. DMF treatment at the concen- trations of 500 µM was able to signiﬁcantly reduce cell viability by 41% on CAL27 cells (A), 43% on HSC-2 (B) cells and 46% on HSC-3 cells (C). DMF 1 mM was able to reduce cell viability by 31% on CAL27 cells, 34% on HSC-2 cells and 33% on HSC-3 cells. DMF 10 mM reduced cell viability by 21% on CAL27 cells, 23% on HSC-2 cells and 24% on HSC-3 cells.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques:

Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 2. Effect of DMF on HO-1 and MnSOD expression in CAL27 cells. The blots revealed a signiﬁcant increase of HO-1 expression following DMF treatment at the concentration of 1 mM and 10 mM (A). DMF at the same doses was also able to signiﬁcant increase the expression of MnSOD (B). (A,B) * p < 0.05 vs. CAL27; ** p < 0.01 vs. CAL27; *** p < 0.001 vs. CAL27.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques: Expressing, Concentration Assay

Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 5. Effect of DMF on CAL27 migration. The wound healing assay (scratch test) revealed a signiﬁcant reduction in the number of cells migrating to the scratched area, following 48 h of DMF treatment at the concentration of 1 mM and 10 mM. ** p < 0.01 vs. CAL27.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques: Migration, Wound Healing Assay, Concentration Assay

Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 7. Effect of DMF on tumor growth in CAL27 orthotopic model. DMF treatment at doses of 30 and 100 mg/kg was able to signiﬁcantly reduce submucosa tumor mass of the tongue and neutrophilic inﬁltration compared to control group (A). No important weight differences were detected between animals (B). Data are representative of at least three independent experiments. Sections were observed and photographed at 10× magniﬁcation. *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC; ### p < 0.001 vs. OSCC.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques: Control

Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 8. Effect of DMF on Caspase3, BAD and BCL-2 expression in tongue samples (A–C). The blots revealed an increase of pro-apoptotic BAD expression after DMF treatment especially at the dose of 100 mg/kg and Caspase 3 at both doses. A decrease of anti-apoptotic BCL-2 expression followed DMF treatment in a dose dependent manner compared to OSCC group. Data are representative of at least three independent experiments. (A,B) ## p < 0.01 vs. OSCC; (C) *** p < 0.001 vs. SHAM; ## p < 0.01 vs. OSCC.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques: Expressing

Journal: International journal of molecular sciences

Article Title: Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition.

doi: 10.3390/ijms24032777

Figure Lengend Snippet: Figure 9. Effect of DMF on HO-1 and MnSOD expression in tongue samples (A,B). The blots revealed a signiﬁcant increase of antioxidant expression of HO-1 after DMF treatment especially at the dose of 100 mg/kg and MnSOD at both doses. (A) * p < 0.05 vs. SHAM; ## p < 0.01 vs. OSCC; (B) ** p < 0.01 vs. SHAM; # p < 0.05 vs. OSCC.

Article Snippet: Cell Cultures Human OSCC cell lines CAL27, HSC-2 and HSC-3 were obtained from ATCC American Type Culture Collection, Rockville, MD, USA).

Techniques: Expressing

(a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary OSCC specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: (a) Molecular structure of the EDB-FN-specific contrast agent MT218. (b-d) Immunohistochemical staining of EDB-FN in human tissues with the EDB-FN-specific G4 antibody was (b) weak in normal tongue specimens (n=3), (c) strong in untreated primary OSCC specimens (n=7), (d) strong in OSCC metastatic specimens (n=2), and (e) moderate in neoadjuvant primary OSCC specimens (n=3). Scale bars in all panels: 200 μm.

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Immunohistochemical staining, Staining

(a) qRT-PCR mRNA analysis (n=3) and (b) western blot protein analysis (n=3) revealed differential and upregulated expression of EDB-FN in aggressive HSC3 and SCC4 cells. (c) Peptide binding study of spheroids with EDB-FN-specific ZD2-Cy5.5 (n=3) showed strong staining in HSC3 and SCC4 spheroids, but not CAL27 spheroids. Quantification of confocal images revealed (d) larger spheroids and (e) stronger ZD2-Cy5.5 staining in HSC3 and SCC4 spheroids in accordance with their EDB-FN expression levels. Data was analyzed with One-Way ANOVA and Fisher’s least significant difference post-hoc tests (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05). Scale bars for confocal images: 200 μm.

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: (a) qRT-PCR mRNA analysis (n=3) and (b) western blot protein analysis (n=3) revealed differential and upregulated expression of EDB-FN in aggressive HSC3 and SCC4 cells. (c) Peptide binding study of spheroids with EDB-FN-specific ZD2-Cy5.5 (n=3) showed strong staining in HSC3 and SCC4 spheroids, but not CAL27 spheroids. Quantification of confocal images revealed (d) larger spheroids and (e) stronger ZD2-Cy5.5 staining in HSC3 and SCC4 spheroids in accordance with their EDB-FN expression levels. Data was analyzed with One-Way ANOVA and Fisher’s least significant difference post-hoc tests (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05). Scale bars for confocal images: 200 μm.

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Quantitative RT-PCR, Western Blot, Expressing, Binding Assay, Staining

(a) Cells grown in 2D and 3D culture (n=3) showed high-risk features in HSC3 and SCC4 cells, but not CAL27 cells. (b) Transwell migration and invasion assays (n=3) demonstrated high invasive potential of HSC3 and SCC4 cells, but not CAL27 cells. Scale bars in all panels: 400 μm.

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: (a) Cells grown in 2D and 3D culture (n=3) showed high-risk features in HSC3 and SCC4 cells, but not CAL27 cells. (b) Transwell migration and invasion assays (n=3) demonstrated high invasive potential of HSC3 and SCC4 cells, but not CAL27 cells. Scale bars in all panels: 400 μm.

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Migration

CNR analysis of contrast-enhanced tumors revealed (a) significant differential enhancement between CAL27, HSC3, and SCC4 tumors with MT218 in accordance with their EDB-FN expression, while (b) gadoteridol showed no difference in enhancement between the three models. Enhancement with MT218 was (c) generally lower than gadoteridol in CAL27 tumors, (d) generally higher than gadoteridol in HSC3 tumors, and (e) substantially higher than gadoteridol in SCC4 tumors. Maximum CNR enhancement in subjects with MT218 was (f) borderline lower than gadoteridol in CAL27 tumors (p=0.0957), (g) borderline higher than gadoteridol in HSC3 tumors (p=0.0639), and (h) significantly higher than gadoteridol in SCC4 tumors. (f-h) Open dots connected with a solid line represent matched mouse-by-mouse data, and solid dots connected with a dotted line represent cohort averages. (i) Average maximum CNR enhancement was significantly different between the three tumor models in accordance with their EDB-FN expression with MT218, but not with gadoteridol. Data was analyzed with Two-Way ANOVA and Fisher’s least significant difference post-hoc test (a-e,i) and unpaired T-tests (f-h) (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05).

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: CNR analysis of contrast-enhanced tumors revealed (a) significant differential enhancement between CAL27, HSC3, and SCC4 tumors with MT218 in accordance with their EDB-FN expression, while (b) gadoteridol showed no difference in enhancement between the three models. Enhancement with MT218 was (c) generally lower than gadoteridol in CAL27 tumors, (d) generally higher than gadoteridol in HSC3 tumors, and (e) substantially higher than gadoteridol in SCC4 tumors. Maximum CNR enhancement in subjects with MT218 was (f) borderline lower than gadoteridol in CAL27 tumors (p=0.0957), (g) borderline higher than gadoteridol in HSC3 tumors (p=0.0639), and (h) significantly higher than gadoteridol in SCC4 tumors. (f-h) Open dots connected with a solid line represent matched mouse-by-mouse data, and solid dots connected with a dotted line represent cohort averages. (i) Average maximum CNR enhancement was significantly different between the three tumor models in accordance with their EDB-FN expression with MT218, but not with gadoteridol. Data was analyzed with Two-Way ANOVA and Fisher’s least significant difference post-hoc test (a-e,i) and unpaired T-tests (f-h) (*, p<0.05; **, p<0.01; ***, p<0.001; n.s., p>0.05).

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Expressing

(a) CAL27 tumors (n=5 for pre, 10, 20, and 30 minutes, n=4 for 40 minutes) showed slightly less enhancement with MT218 than gadoteridol. (b) HSC3 tumors (n=4) showed slightly more enhancement with MT218 than gadoteridol. (c) SCC4 tumors (n=4) showed substantially more enhancement with MT218 than gadoteridol. MT218 and gadoteridol were used at doses of 0.04 mmol/kg and 0.10 mmol/kg, respectively.

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: (a) CAL27 tumors (n=5 for pre, 10, 20, and 30 minutes, n=4 for 40 minutes) showed slightly less enhancement with MT218 than gadoteridol. (b) HSC3 tumors (n=4) showed slightly more enhancement with MT218 than gadoteridol. (c) SCC4 tumors (n=4) showed substantially more enhancement with MT218 than gadoteridol. MT218 and gadoteridol were used at doses of 0.04 mmol/kg and 0.10 mmol/kg, respectively.

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques:

(a) H&E staining of OSCC xenografts (n=3) showed various morphological features and stages of differentiation. (b) Immunohistochemistry for EDB-FN with the EDB-FN-specific G4 antibody (n=3) showed weak, moderate and strong staining in the epithelial regions of CAL27, HSC3, and SCC4 tumors, respectively, with little nonspecific staining. Scale bars: 600μm for H&E images, 200μm for immunohistochemistry images.

Journal: Molecular imaging and biology

Article Title: Preclinical assessment of the effectiveness of magnetic resonance molecular imaging of extradomain-B fibronectin for detection and characterization of oral cancer

doi: 10.1007/s11307-020-01524-6

Figure Lengend Snippet: (a) H&E staining of OSCC xenografts (n=3) showed various morphological features and stages of differentiation. (b) Immunohistochemistry for EDB-FN with the EDB-FN-specific G4 antibody (n=3) showed weak, moderate and strong staining in the epithelial regions of CAL27, HSC3, and SCC4 tumors, respectively, with little nonspecific staining. Scale bars: 600μm for H&E images, 200μm for immunohistochemistry images.

Article Snippet: Cell culture Human OSCC cell lines CAL27 and SCC4 were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA).

Techniques: Staining, Immunohistochemistry

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cell cultures human oscc cell lines cal27 (ATCC)

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1) Product Images from "Therapeutic Potential of Dimethyl Fumarate in Counteract Oral Squamous Cell Carcinoma Progression by Modulating Apoptosis, Oxidative Stress and Epithelial-Mesenchymal Transition."

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