cervical carcinoma hela Search Results


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China Center for Type Culture Collection human hela cells gdc0009
Knockdown of FLNB promotes proliferation and inhibits apoptosis of <t>HeLa</t> <t>cells.</t> (A) Relative mRNA expression of FLNB in HeLa cells after it was knocked down using FLNB -specific shRNA was determined by reverse transcription-qPCR. shFLNB_1 and shFLNB_2 indicate two biological repeats of HeLa cells transfected with FLNB-specific shRNA. Ctrl_1 and Ctrl_2 indicate two biological repeats of HeLa cells transfected with empty vector as controls. (B) Cell proliferation of shFLNB was measured by an MTT assay in HeLa cells. Cell apoptosis of cells transfected with shFLNB was measured by (C) flow cytometry and (D) subsequent analysis by a 7-ADD and Annexin V assay. *P<0.05 and **P<0.01 vs. respective Ctrl. FLNB , filamin B; sh, short hairpin; qPCR, quantitative PCR; Ctrl, control; 7-AAD, 7-amino actinomycin D; OD, optical density; PE, phycoerythrin.
Human Hela Cells Gdc0009, supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioResource International Inc hela cervical carcinoma id 60005
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Hela Cervical Carcinoma Id 60005, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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BioResource International Inc human cervical carcinoma cell line hela cells
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Human Cervical Carcinoma Cell Line Hela Cells, supplied by BioResource International Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Coriell Institute for Medical Research cervical carcinoma cell lines c33a and hela
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Cervical Carcinoma Cell Lines C33a And Hela, supplied by Coriell Institute for Medical Research, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson human cervical carcinoma lysate hela cells bd-611450
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Human Cervical Carcinoma Lysate Hela Cells Bd 611450, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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China Center for Type Culture Collection human cervical carcinoma (hela)
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Human Cervical Carcinoma (Hela), supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Beijing Xiehe Pharmaceutical Co Ltd human cervical carcinoma hela
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Human Cervical Carcinoma Hela, supplied by Beijing Xiehe Pharmaceutical Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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hela  (ATCC)
99
ATCC hela
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Hela, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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China Center for Type Culture Collection cervical carcinoma hela cell line gdc009
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Cervical Carcinoma Hela Cell Line Gdc009, supplied by China Center for Type Culture Collection, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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iCell Bioscience Inc human cervical carcinoma cell line hela
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Human Cervical Carcinoma Cell Line Hela, supplied by iCell Bioscience Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cervical+carcinoma+hela/human+cervical+carcinoma+cell+line+hela/10__1016_slash_j__molliq__2019__111822-34-2-22
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Nanogen Inc metastatic human cervical carcinoma cell line hela cells
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
Metastatic Human Cervical Carcinoma Cell Line Hela Cells, supplied by Nanogen Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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FineTest Biotech Inc human cervical carcinoma cells hela
Cross-talk between phenformin and DEC1 in <t>HeLa</t> <t>and</t> <t>A2058</t> cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.
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Image Search Results


Knockdown of FLNB promotes proliferation and inhibits apoptosis of HeLa cells. (A) Relative mRNA expression of FLNB in HeLa cells after it was knocked down using FLNB -specific shRNA was determined by reverse transcription-qPCR. shFLNB_1 and shFLNB_2 indicate two biological repeats of HeLa cells transfected with FLNB-specific shRNA. Ctrl_1 and Ctrl_2 indicate two biological repeats of HeLa cells transfected with empty vector as controls. (B) Cell proliferation of shFLNB was measured by an MTT assay in HeLa cells. Cell apoptosis of cells transfected with shFLNB was measured by (C) flow cytometry and (D) subsequent analysis by a 7-ADD and Annexin V assay. *P<0.05 and **P<0.01 vs. respective Ctrl. FLNB , filamin B; sh, short hairpin; qPCR, quantitative PCR; Ctrl, control; 7-AAD, 7-amino actinomycin D; OD, optical density; PE, phycoerythrin.

Journal: Oncology Reports

Article Title: Filamin B extensively regulates transcription and alternative splicing, and is associated with apoptosis in HeLa cells

doi: 10.3892/or.2020.7532

Figure Lengend Snippet: Knockdown of FLNB promotes proliferation and inhibits apoptosis of HeLa cells. (A) Relative mRNA expression of FLNB in HeLa cells after it was knocked down using FLNB -specific shRNA was determined by reverse transcription-qPCR. shFLNB_1 and shFLNB_2 indicate two biological repeats of HeLa cells transfected with FLNB-specific shRNA. Ctrl_1 and Ctrl_2 indicate two biological repeats of HeLa cells transfected with empty vector as controls. (B) Cell proliferation of shFLNB was measured by an MTT assay in HeLa cells. Cell apoptosis of cells transfected with shFLNB was measured by (C) flow cytometry and (D) subsequent analysis by a 7-ADD and Annexin V assay. *P<0.05 and **P<0.01 vs. respective Ctrl. FLNB , filamin B; sh, short hairpin; qPCR, quantitative PCR; Ctrl, control; 7-AAD, 7-amino actinomycin D; OD, optical density; PE, phycoerythrin.

Article Snippet: Human HeLa cells (CCTCC@GDC0009) were obtained from The China Center for Type Culture Collection.

Techniques: Knockdown, Expressing, shRNA, Reverse Transcription, Transfection, Plasmid Preparation, MTT Assay, Flow Cytometry, Annexin V Assay, Real-time Polymerase Chain Reaction, Control

GO and KEGG analysis of differentially expressed genes between short hairpin FLNB-transfected and control HeLa cells. Top 10 most enriched GO terms (biological process) of (A) upregulated and (B) downregulated genes upon FLNB knockdown. Rectangles around GO terms indicate notable cancer-related and cartilage development terms. Top 10 most enriched KEGG pathways of (C) upregulated and (D) downregulated genes upon FLNB knockdown. GO, Gene Ontology; KEGG, Kyoto Encyclopedia of Genes and Genomes; FLNB , filamin B.

Journal: Oncology Reports

Article Title: Filamin B extensively regulates transcription and alternative splicing, and is associated with apoptosis in HeLa cells

doi: 10.3892/or.2020.7532

Figure Lengend Snippet: GO and KEGG analysis of differentially expressed genes between short hairpin FLNB-transfected and control HeLa cells. Top 10 most enriched GO terms (biological process) of (A) upregulated and (B) downregulated genes upon FLNB knockdown. Rectangles around GO terms indicate notable cancer-related and cartilage development terms. Top 10 most enriched KEGG pathways of (C) upregulated and (D) downregulated genes upon FLNB knockdown. GO, Gene Ontology; KEGG, Kyoto Encyclopedia of Genes and Genomes; FLNB , filamin B.

Article Snippet: Human HeLa cells (CCTCC@GDC0009) were obtained from The China Center for Type Culture Collection.

Techniques: Transfection, Control, Knockdown

Validation of FLNB -regulated genes (DEGs). (A) Relative expression level (FPKM, up) and RT-qPCR measurement (down) of cartilage development-related DEGs. (B) Related expression level (FPKM, up) and RT-qPCR measurement (down) of apoptotic-related DEGs. (C) Western blot analysis of two apoptotic-related proteins in shFLNB and Ctrl HeLa cells. FLNB , filamin B; DEGs, differentially expressed genes; FPKM, fragments per kilobase of transcript per million fragments mapped; RT-qPCR, reverse transcription-quantitative PCR; sh, short hairpin; Ctrl, control; ATP7A, ATPase copper transporting α; BMP7, bone morphogenetic protein 7; COL2A1, collagen type II α 1 chain; MMP13, matrix metallopeptidase 13; IL23A, interleukin 23 subunit α; MALAT1, metastasis associated lung adenocarcinoma transcript 1; NAIP, NLR family apoptosis inhibitory protein; SLC25A36, solute carrier family 25 member 36; MAP2K7, mitogen-activated protein kinase kinase 7.

Journal: Oncology Reports

Article Title: Filamin B extensively regulates transcription and alternative splicing, and is associated with apoptosis in HeLa cells

doi: 10.3892/or.2020.7532

Figure Lengend Snippet: Validation of FLNB -regulated genes (DEGs). (A) Relative expression level (FPKM, up) and RT-qPCR measurement (down) of cartilage development-related DEGs. (B) Related expression level (FPKM, up) and RT-qPCR measurement (down) of apoptotic-related DEGs. (C) Western blot analysis of two apoptotic-related proteins in shFLNB and Ctrl HeLa cells. FLNB , filamin B; DEGs, differentially expressed genes; FPKM, fragments per kilobase of transcript per million fragments mapped; RT-qPCR, reverse transcription-quantitative PCR; sh, short hairpin; Ctrl, control; ATP7A, ATPase copper transporting α; BMP7, bone morphogenetic protein 7; COL2A1, collagen type II α 1 chain; MMP13, matrix metallopeptidase 13; IL23A, interleukin 23 subunit α; MALAT1, metastasis associated lung adenocarcinoma transcript 1; NAIP, NLR family apoptosis inhibitory protein; SLC25A36, solute carrier family 25 member 36; MAP2K7, mitogen-activated protein kinase kinase 7.

Article Snippet: Human HeLa cells (CCTCC@GDC0009) were obtained from The China Center for Type Culture Collection.

Techniques: Biomarker Discovery, Expressing, Quantitative RT-PCR, Western Blot, Reverse Transcription, Real-time Polymerase Chain Reaction, Control

Validation of FLNB -affected ASEs. Genome visualization (left panel) shows FLNB -regulated ASEs in shFLNB and control. (A) Validation of an ASE of VDR in HeLa cells. (B) Validation of an ASE of PACS2 in HeLa cells. (C) Validation of an ASE of MAP2K7 in HeLa cells. (D) Validation of an ASE of MALAT1 in HeLa cells. The number of junction reads were marked on the line representing splice junction composing ASE. The structures of ASEs are depicted in the top-right panel. The altered ratio of ASEs in RNA-sequencing and in reverse transcription-quantitative PCR were calculated and plotted (right panel, bottom). FLNB , filamin B; ASEs, alternative splicing events; sh/SH, short hairpin; NC, negative control; VDR, vitamin D receptor; PACS2, phosphofurin acidic cluster sorting protein 2; MAP2K7, mitogen-activated protein kinase kinase 7; MALAT1, metastasis associated lung adenocarcinoma transcript 1. *P<0.05 and ***P<0.001 vs. respectively NC.

Journal: Oncology Reports

Article Title: Filamin B extensively regulates transcription and alternative splicing, and is associated with apoptosis in HeLa cells

doi: 10.3892/or.2020.7532

Figure Lengend Snippet: Validation of FLNB -affected ASEs. Genome visualization (left panel) shows FLNB -regulated ASEs in shFLNB and control. (A) Validation of an ASE of VDR in HeLa cells. (B) Validation of an ASE of PACS2 in HeLa cells. (C) Validation of an ASE of MAP2K7 in HeLa cells. (D) Validation of an ASE of MALAT1 in HeLa cells. The number of junction reads were marked on the line representing splice junction composing ASE. The structures of ASEs are depicted in the top-right panel. The altered ratio of ASEs in RNA-sequencing and in reverse transcription-quantitative PCR were calculated and plotted (right panel, bottom). FLNB , filamin B; ASEs, alternative splicing events; sh/SH, short hairpin; NC, negative control; VDR, vitamin D receptor; PACS2, phosphofurin acidic cluster sorting protein 2; MAP2K7, mitogen-activated protein kinase kinase 7; MALAT1, metastasis associated lung adenocarcinoma transcript 1. *P<0.05 and ***P<0.001 vs. respectively NC.

Article Snippet: Human HeLa cells (CCTCC@GDC0009) were obtained from The China Center for Type Culture Collection.

Techniques: Biomarker Discovery, Control, RNA Sequencing, Reverse Transcription, Real-time Polymerase Chain Reaction, Alternative Splicing, Negative Control

Cross-talk between phenformin and DEC1 in HeLa and A2058 cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.

Journal: Cancer Management and Research

Article Title: The antitumor properties of metformin and phenformin reflect their ability to inhibit the actions of differentiated embryo chondrocyte 1

doi: 10.2147/CMAR.S210637

Figure Lengend Snippet: Cross-talk between phenformin and DEC1 in HeLa and A2058 cells. ( A and B ) HeLa cells were treated for 16 h with the indicated concentration of phenformin. Cell lysates were then subjected to ( A ) RT-PCR or ( B ) Western blot analysis of p53, p21, DEC1, and survivin. GAPDH was the mRNA loading control, while ACTN was the protein loading control. PCR and protein bands (A and B) were quantified through pixel density scanning and evaluated using ImageJ. The fold was normalized to the control for the gene or protein. ( C and D ) DEC1 was knocked down in ( C ) HeLa and ( D ) A2058 cells, which were then treated for 16 h with the indicated concentration of phenformin. Cell lysates were subjected to Western blot analysis using antibodies against p53, survivin, cyclin D1, and DEC1. PCNA was the protein loading control. Protein bands ( C and D ) were quantified through pixel density scanning and evaluated using ImageJ. The fold was compared with shLUC, normalized to the internal control protein PCNA. The results are representative of three independent experiments.

Article Snippet: HeLa cervical carcinoma (ID 60005) and A2058 melanoma (ID 60240) cells were purchased from the Bioresource Collection and Research Center, Taiwan, Republic of China.

Techniques: Concentration Assay, Reverse Transcription Polymerase Chain Reaction, Western Blot, Control

Effects of phenformin and DEC1 on the cell cycle profile of HeLa and A2058 cells. DEC1 was knocked down in ( A ) HeLa and ( B ) A2058 cells, which were then treated for 30 h with the indicated concentration of phenformin. Cell lysates were subjected to cell cycle profiling using flow cytometry. The results are representative of two independent experiments.

Journal: Cancer Management and Research

Article Title: The antitumor properties of metformin and phenformin reflect their ability to inhibit the actions of differentiated embryo chondrocyte 1

doi: 10.2147/CMAR.S210637

Figure Lengend Snippet: Effects of phenformin and DEC1 on the cell cycle profile of HeLa and A2058 cells. DEC1 was knocked down in ( A ) HeLa and ( B ) A2058 cells, which were then treated for 30 h with the indicated concentration of phenformin. Cell lysates were subjected to cell cycle profiling using flow cytometry. The results are representative of two independent experiments.

Article Snippet: HeLa cervical carcinoma (ID 60005) and A2058 melanoma (ID 60240) cells were purchased from the Bioresource Collection and Research Center, Taiwan, Republic of China.

Techniques: Concentration Assay, Flow Cytometry