Transwell assays were performed to assess the migration of (A) S2-013, (B) BxPC-3, (C) MIA PaCa-2, (D) T3M-4, and (E) CFPAC-1 cells following treatment with 1 μM or 10 μM of M344 (or with 0.1% DMSO, as the vehicle control) for 24 h. For the transwell assays, after treatment the cells were plated into 3 separate 8-μm inserts (1x105 cells/insert) in the presence of 1 μM M344, 10 μM M344, or 0.1% DMSO and incubated for 24 h. Cells were fixed and stained, and photographs of 3 random fields were taken for each of the inserts. The results of counts of the stained, migrated cells were averaged. The graph shows the average numbers of cells that migrated, and each error bar represents the standard error of the mean. The presented graph for the S2-01...
(A) NCCIT scramble, Np9 KD clones 8 and 9 with H2B-mCherry control clones and NCCIT Np9 KD clones 8 ...
Abstract Background Migration of cancer cell correlates with distant metastasis and local invasion, ...
(A) B16.F10 cells co-cultured with TAMs before administration (T = 0) and 24 h after administration ...
These transwell migration assay data correspond to the graph that is displayed in Fig 5, and the exp...
After treatment with M344 at various concentrations, the proliferation of (A) S2-013, (B) BxPC-3, (C...
After treatment with M344 at various concentrations, the viability of (A) S2-013, (B) BxPC-3, (C) MI...
<p>(A)Cells were plated onto uncoated plates and after 24 hours the monolayer was scraped with a 10 ...
<p>(A) Wound healing assay was performed to evaluate the migration of PANC-1 and HPAC cells after si...
<p>(A-D) Miapaca-2, Panc-1, SNU-213 cells, and HUVECs were incubated with varying doses of kaempfero...
<p>Cells were treated with 10 µM TCP, ChlA, BA, CA, TDI, AMN, MER or ROX for 24 hours. (<b>A</b>) Pe...
After 24- or 48-hour treatments with 0.1% DMSO (vehicle control) or with M344 at 5 or 10 μM concentr...
<p>The cell migration and invasion capacity of pancreatic cancer cells treated with conditioned medi...
<p>Inhibition of tumour migration by a Boyden chamber assay. CaCo-2, HT29 and SW480 cells were plate...
<p><b>A</b>) ‘Wound healing’ assay. A confluent layer of L3.6pl was scratched and either left untrea...
<p>(A) A Boyden chamber assay was used to measure the migration of gastric cancer cells. 10% FBS was...
(A) NCCIT scramble, Np9 KD clones 8 and 9 with H2B-mCherry control clones and NCCIT Np9 KD clones 8 ...
Abstract Background Migration of cancer cell correlates with distant metastasis and local invasion, ...
(A) B16.F10 cells co-cultured with TAMs before administration (T = 0) and 24 h after administration ...
These transwell migration assay data correspond to the graph that is displayed in Fig 5, and the exp...
After treatment with M344 at various concentrations, the proliferation of (A) S2-013, (B) BxPC-3, (C...
After treatment with M344 at various concentrations, the viability of (A) S2-013, (B) BxPC-3, (C) MI...
<p>(A)Cells were plated onto uncoated plates and after 24 hours the monolayer was scraped with a 10 ...
<p>(A) Wound healing assay was performed to evaluate the migration of PANC-1 and HPAC cells after si...
<p>(A-D) Miapaca-2, Panc-1, SNU-213 cells, and HUVECs were incubated with varying doses of kaempfero...
<p>Cells were treated with 10 µM TCP, ChlA, BA, CA, TDI, AMN, MER or ROX for 24 hours. (<b>A</b>) Pe...
After 24- or 48-hour treatments with 0.1% DMSO (vehicle control) or with M344 at 5 or 10 μM concentr...
<p>The cell migration and invasion capacity of pancreatic cancer cells treated with conditioned medi...
<p>Inhibition of tumour migration by a Boyden chamber assay. CaCo-2, HT29 and SW480 cells were plate...
<p><b>A</b>) ‘Wound healing’ assay. A confluent layer of L3.6pl was scratched and either left untrea...
<p>(A) A Boyden chamber assay was used to measure the migration of gastric cancer cells. 10% FBS was...
(A) NCCIT scramble, Np9 KD clones 8 and 9 with H2B-mCherry control clones and NCCIT Np9 KD clones 8 ...
Abstract Background Migration of cancer cell correlates with distant metastasis and local invasion, ...
(A) B16.F10 cells co-cultured with TAMs before administration (T = 0) and 24 h after administration ...