miapaca2 atcc Search Results


97
ATCC miapaca2
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Miapaca2, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC miapaca 2
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Miapaca 2, 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
https://www.bioz.com/product/miapaca2+atcc/MIA+PaCa-2/pmc02823521-78-2-11
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96
ATCC human cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Human Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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99
ATCC cancer cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Cancer Cell Lines, 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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99
ATCC pancreatic cancer cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Pancreatic Cancer Cell Lines, 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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97
ATCC pc cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Pc Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
DSMZ miapaca2 atcc
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Miapaca2 Atcc, supplied by DSMZ, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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95
ATCC human pancreatic cancer cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Human Pancreatic Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/miapaca2+atcc/Capan-1%3B+Pancreatic+Carcinoma%3B+Human/pmc04167492-50-0-11
Average 95 stars, based on 1 article reviews
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99
ATCC cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Cell Lines, 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
https://www.bioz.com/product/miapaca2+atcc/PANC-1/pmc06445724-82-1-12
Average 99 stars, based on 1 article reviews
cell lines - by Bioz Stars, 2026-09
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97
ATCC cell culture human pancreatic cancer cell lines
(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of <t>MiaPaCa2</t> cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.
Cell Culture Human Pancreatic Cancer Cell Lines, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/miapaca2+atcc/HPAF-II/pmc02895953-62-0-18
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96
ATCC human pdac cell line miapaca2
A. Kras-induced constitutive NF-κB expression was measured by Western blot analysis in HPNE, HPNE/Vec, HPNE/KrasG12V, HPNE/KrasG12V/P16sh, <t>MiaPaca2,</t> and Colo357 cell lines; B. NF-κB expression levels in HPNE/KrasG12V, HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells were significantly higher than in HPNE and HPNE/Vec cells; C, Western blot analysis shows phosphorylated NF-κB expression in nuclear extract of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; D, electrophoretic mobility shift assay shows phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh cells treated with 50, 100, or 200 μM NBDP; E, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; F and G, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of MiaPaca2 and Colo357 cells treated with 50, 100, or 200 μM NBDP. IOD: integrated optical density
Human Pdac Cell Line Miapaca2, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/miapaca2+atcc/Clone+of+Human+cell+Line+6D9/pmc06415976-236-1-10
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Image Search Results


(C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of MiaPaCa2 cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.

Journal: PLoS ONE

Article Title: Retinoid Signaling in Pancreatic Cancer, Injury and Regeneration

doi: 10.1371/journal.pone.0029075

Figure Lengend Snippet: (C) CRBP1 methylation status in PC cell lines and (D) restoration of CRBP1 expression with combination treatment of MiaPaCa2 cells with 5-Aza and TSA. (E) CRBP1 knockdown in stably transfected HPDE-EcoR cells. (F) HPDE cells grown in 3D demonstrate no change in morphology between siCRBP1 cells and scrambled control.

Article Snippet: Six pancreatic cancer cell lines were used: AsPC-1, BxPC-3, Capan-2, HPAC, MiaPaCa2 and PANC1 (ATCC, VA, USA).

Techniques: Methylation, Expressing, Knockdown, Stable Transfection, Transfection, Control

A. Kras-induced constitutive NF-κB expression was measured by Western blot analysis in HPNE, HPNE/Vec, HPNE/KrasG12V, HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cell lines; B. NF-κB expression levels in HPNE/KrasG12V, HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells were significantly higher than in HPNE and HPNE/Vec cells; C, Western blot analysis shows phosphorylated NF-κB expression in nuclear extract of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; D, electrophoretic mobility shift assay shows phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh cells treated with 50, 100, or 200 μM NBDP; E, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; F and G, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of MiaPaca2 and Colo357 cells treated with 50, 100, or 200 μM NBDP. IOD: integrated optical density

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A. Kras-induced constitutive NF-κB expression was measured by Western blot analysis in HPNE, HPNE/Vec, HPNE/KrasG12V, HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cell lines; B. NF-κB expression levels in HPNE/KrasG12V, HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells were significantly higher than in HPNE and HPNE/Vec cells; C, Western blot analysis shows phosphorylated NF-κB expression in nuclear extract of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; D, electrophoretic mobility shift assay shows phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh cells treated with 50, 100, or 200 μM NBDP; E, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of HPNE/KrasG12V/P16sh cells treated with 50, 100, or200 μM NBDP; F and G, Western blot analysis shows phosphorylated NF-κB expression in total cell lysates of MiaPaca2 and Colo357 cells treated with 50, 100, or 200 μM NBDP. IOD: integrated optical density

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Expressing, Western Blot, Electrophoretic Mobility Shift Assay

A. Immunoprecipitation analysis showed that TNF-α (10 ng/mL) factor stimulated and promoted IKKγ to combine with IKKβ in HPNE/KrasG12V/P16sh cells; NBDP (100 μM) was competitive with IKKβ, decreasing the IKK γ combination under TNF-α (10 ng/mL) factor stimulation; B. Western blot analysis showed the change of NF-κB pathway in HPNE/KrasG12V/P16sh cells treated with NBDP (100 μM); C. Western blot analysis measured phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh cells treated with gemcitabine (10 μM) in 0 h, 1 h, 2 h, 4 h, 6 h, 12 h; D. phosphorylated NF-κB expression was significantly increased in HPNE/KrasG12V and HPNE/KrasG12V/P16sh cells treated with gemcitabine at 2 h and 4 h (2 h vs 0 h, *P=0.0118; 4 h vs 0 h, **P=0.0029); E. Western blot analysis measured phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells treated with gemcitabine (10 μM) combined with NBDP (100 μM); F. NBDP decreased gemcitabine chemo-resistance due to increased phosphorylated NF-κB expressions in HPNE/KrasG12V/P16sh (gemcitabine vs control, *P=0.0001; combination vs gemcitabine, **P<0.0001), MiaPaca2 (gemcitabine vs control, *P<0.0001; combination vs gemcitabine, **P=0.0002), and Colo357 (gemcitabine vs control, *P=0.0014; combination vs gemcitabine, **P=0.0005) cell lines. Gem: gemcitabine; IOD: integrated optical density.

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A. Immunoprecipitation analysis showed that TNF-α (10 ng/mL) factor stimulated and promoted IKKγ to combine with IKKβ in HPNE/KrasG12V/P16sh cells; NBDP (100 μM) was competitive with IKKβ, decreasing the IKK γ combination under TNF-α (10 ng/mL) factor stimulation; B. Western blot analysis showed the change of NF-κB pathway in HPNE/KrasG12V/P16sh cells treated with NBDP (100 μM); C. Western blot analysis measured phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh cells treated with gemcitabine (10 μM) in 0 h, 1 h, 2 h, 4 h, 6 h, 12 h; D. phosphorylated NF-κB expression was significantly increased in HPNE/KrasG12V and HPNE/KrasG12V/P16sh cells treated with gemcitabine at 2 h and 4 h (2 h vs 0 h, *P=0.0118; 4 h vs 0 h, **P=0.0029); E. Western blot analysis measured phosphorylated NF-κB expression in HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells treated with gemcitabine (10 μM) combined with NBDP (100 μM); F. NBDP decreased gemcitabine chemo-resistance due to increased phosphorylated NF-κB expressions in HPNE/KrasG12V/P16sh (gemcitabine vs control, *P=0.0001; combination vs gemcitabine, **P<0.0001), MiaPaca2 (gemcitabine vs control, *P<0.0001; combination vs gemcitabine, **P=0.0002), and Colo357 (gemcitabine vs control, *P=0.0014; combination vs gemcitabine, **P=0.0005) cell lines. Gem: gemcitabine; IOD: integrated optical density.

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Immunoprecipitation, Western Blot, Expressing, Control

A. MTT analysis showed that proliferation of HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells was inhibited by NBDP at doses of 5, 10, 25, 50, 100, 200, and 400 μM within 5 days; B. MTT analysis showed that proliferation of HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells was inhibited by gemcitabine at doses of 250 and 500 nM and 1, 5, 10, and 20 μM within 5 days; C. IC50 values of NBDP were detected by MTT analysis in HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells; D. MTT analysis showed that NBDP combined with gemcitabine inhibited proliferation in HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells. Ctrl: control; Gem: gemcitabine; IOD: integrated optical density.

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A. MTT analysis showed that proliferation of HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells was inhibited by NBDP at doses of 5, 10, 25, 50, 100, 200, and 400 μM within 5 days; B. MTT analysis showed that proliferation of HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells was inhibited by gemcitabine at doses of 250 and 500 nM and 1, 5, 10, and 20 μM within 5 days; C. IC50 values of NBDP were detected by MTT analysis in HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells; D. MTT analysis showed that NBDP combined with gemcitabine inhibited proliferation in HPNE/KrasG12V/P16sh, MiaPaca2, and Colo357 cells. Ctrl: control; Gem: gemcitabine; IOD: integrated optical density.

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Control

A. Colony formation analysis showed that tumor cell proliferation was inhibited by NBDP at doses of 50, 100, and 200 μM in HPNE/KrasG12V/P16sh (50 μM NBDP vs control, *P=0.0004), MiaPaca2 (50 μM NBDP vs control, *P=0.0085), and Colo357 (50 μM NBDP vs control, *P=0.0218) cells; B. Colony formation analysis showed that NBDP treatment combined with gemcitabine inhibited proliferation of HPNE/KrasG12V/P16sh (NBDP vs control, *P=0.0123; combination vs gemcitabine, **P=0.0165), MiaPaca2 (NBDP vs control, *P=0.0114; combination vs gemcitabine, **P=0.0008), and Colo357 (NBDP vs control, *P=0. 0.0031; combination vs gemcitabine, **P=0.0026) cells; C. Wound-healing analysis showed that NBDP decreased invasion of HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells at doses of 50, 100, and 200 μM. Ctrl: control; Gem: gemcitabine

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A. Colony formation analysis showed that tumor cell proliferation was inhibited by NBDP at doses of 50, 100, and 200 μM in HPNE/KrasG12V/P16sh (50 μM NBDP vs control, *P=0.0004), MiaPaca2 (50 μM NBDP vs control, *P=0.0085), and Colo357 (50 μM NBDP vs control, *P=0.0218) cells; B. Colony formation analysis showed that NBDP treatment combined with gemcitabine inhibited proliferation of HPNE/KrasG12V/P16sh (NBDP vs control, *P=0.0123; combination vs gemcitabine, **P=0.0165), MiaPaca2 (NBDP vs control, *P=0.0114; combination vs gemcitabine, **P=0.0008), and Colo357 (NBDP vs control, *P=0. 0.0031; combination vs gemcitabine, **P=0.0026) cells; C. Wound-healing analysis showed that NBDP decreased invasion of HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells at doses of 50, 100, and 200 μM. Ctrl: control; Gem: gemcitabine

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Control

A. Flow cytometry analysis of the Annexin V staining assay showed the apoptosis of HPNE/KrasG12V/P16sh cells treated with NBDP at 50, 100, and 200 μM; B. the ratio of apoptosis increased with increasing NBDP doses in HPNE/KrasG12V/P16sh cells (50 μM NBDP vs control, *P=0.0004); C. Flow cytometry analysis showed that 100 μM NBDP combined with 5 μM gemcitabine increased apoptosis in HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells; D. The ratio of apoptosis increased with NBDP combined with gemcitabine in HPNE/KrasG12V/P16sh (NBDP vs control, *P=0.0870; combination vs gemcitabine, **P=0.0061), MiaPaca2 (NBDP vs control, *P=0.0055; combination vs gemcitabine, **P=0.0407), and Colo357 (NBDP vs control, *P=0.0659; combination vs gemcitabine, **P=0.0522) cells. Ctrl: control; Gem: gemcitabine

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A. Flow cytometry analysis of the Annexin V staining assay showed the apoptosis of HPNE/KrasG12V/P16sh cells treated with NBDP at 50, 100, and 200 μM; B. the ratio of apoptosis increased with increasing NBDP doses in HPNE/KrasG12V/P16sh cells (50 μM NBDP vs control, *P=0.0004); C. Flow cytometry analysis showed that 100 μM NBDP combined with 5 μM gemcitabine increased apoptosis in HPNE/KrasG12V /P16sh, MiaPaca2, and Colo357 cells; D. The ratio of apoptosis increased with NBDP combined with gemcitabine in HPNE/KrasG12V/P16sh (NBDP vs control, *P=0.0870; combination vs gemcitabine, **P=0.0061), MiaPaca2 (NBDP vs control, *P=0.0055; combination vs gemcitabine, **P=0.0407), and Colo357 (NBDP vs control, *P=0.0659; combination vs gemcitabine, **P=0.0522) cells. Ctrl: control; Gem: gemcitabine

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Flow Cytometry, Annexin V Staining Assay, Control

A Western blot analysis showed the expression of Parp in HPNE/KrasG12V/P16sh cells treated with NBDP (50, 100, and 200 μM); B. The expression of Parp increased after NBDP treatment in HPNE/KrasG12V/P16sh cells (50 μM NBDP vs control, *P=0.0007); C. Western blot analysis showed the expression of cleaved-Parp and cleaved-caspase 3 in HPNE/KrasG12V/P16sh cells treated with NBDP (100 μM) combined with gemcitabine (10 μM); D–E. cleaved-Parp expression and cleaved-caspase 3 expression were both increased under the combination treatment with NBDP (100 μM) and gemcitabine (10 μM) in HPNE/KrasG12V/P16sh cells (C-Parp: combination vs gemcitabine, **P=0.0235; C-caspase 3: combination vs gemcitabine, **P=0.0075); F–G. MiaPaca2 and Colo357 cells were measured for expression of cleaved-Parp and cleaved-caspase 3 by Western blot analysis after the combination treatment with NBDP (100 μM) and gemcitabine (10 μM); H–K. cleaved-Parp expression and cleaved caspase 3 expression were both increased under the combination treatment with NBDP (100 μM) and gemcitabine (10 μM) in MiaPaca2 (C-Parp: combination vs gemcitabine, **P=0.0017; C-caspase 3: combination vs gemcitabine, **P=0.1033) and Colo357 (C-Parp: combination vs gemcitabine, **P=0.0585; C-caspase 3: gemcitabine vs gemcitabine, **P=0.0032) cells. Gem: gemcitabine; C: cleaved

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: A Western blot analysis showed the expression of Parp in HPNE/KrasG12V/P16sh cells treated with NBDP (50, 100, and 200 μM); B. The expression of Parp increased after NBDP treatment in HPNE/KrasG12V/P16sh cells (50 μM NBDP vs control, *P=0.0007); C. Western blot analysis showed the expression of cleaved-Parp and cleaved-caspase 3 in HPNE/KrasG12V/P16sh cells treated with NBDP (100 μM) combined with gemcitabine (10 μM); D–E. cleaved-Parp expression and cleaved-caspase 3 expression were both increased under the combination treatment with NBDP (100 μM) and gemcitabine (10 μM) in HPNE/KrasG12V/P16sh cells (C-Parp: combination vs gemcitabine, **P=0.0235; C-caspase 3: combination vs gemcitabine, **P=0.0075); F–G. MiaPaca2 and Colo357 cells were measured for expression of cleaved-Parp and cleaved-caspase 3 by Western blot analysis after the combination treatment with NBDP (100 μM) and gemcitabine (10 μM); H–K. cleaved-Parp expression and cleaved caspase 3 expression were both increased under the combination treatment with NBDP (100 μM) and gemcitabine (10 μM) in MiaPaca2 (C-Parp: combination vs gemcitabine, **P=0.0017; C-caspase 3: combination vs gemcitabine, **P=0.1033) and Colo357 (C-Parp: combination vs gemcitabine, **P=0.0585; C-caspase 3: gemcitabine vs gemcitabine, **P=0.0032) cells. Gem: gemcitabine; C: cleaved

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Western Blot, Expressing, Control

The NEMO-binding domain peptide (NBDP) of IKK was found to inhibit NF-κB activation in cancer cells. Mechanistic investigations showed that NBDP effectively competed with IKKγ for binding to IKKs and thus inhibited IKK/IκB/NF-kB pathway activation in PDAC.

Journal: Cancer letters

Article Title: NEMO Peptide Inhibits the Growth of Pancreatic Ductal Adenocarcinoma by Blocking NF-κB Activation

doi: 10.1016/j.canlet.2017.09.018

Figure Lengend Snippet: The NEMO-binding domain peptide (NBDP) of IKK was found to inhibit NF-κB activation in cancer cells. Mechanistic investigations showed that NBDP effectively competed with IKKγ for binding to IKKs and thus inhibited IKK/IκB/NF-kB pathway activation in PDAC.

Article Snippet: The human PDAC cell line MiaPaca2 was purchased from the American Type Culture Collection.

Techniques: Binding Assay, Activation Assay