figshare
Browse
Fig_1.tif (3.16 MB)

PTEN disruption in Chordoma is associated with enhanced in vitro proliferation and invasion.

Download (0 kB)
figure
posted on 2015-08-06, 03:18 authored by Dae-Hee Lee, Ying Zhang, Amin B. Kassam, Myung-Jin Park, Paul GardnerPaul Gardner, Daniel Prevedello, Stephanie Henry, Craig Horbinski, Jan H. Beumer, Hussein Tawbi, Brian J. Williams, Mark E. Shaffrey, Merrill J. Egorin, Roger Abounader, Deric M. Park

(A) A representative immunoblot for PTEN expression demonstrating a decreased level of expression of PTEN in the chordoma specimens with LOH at 10q23 locus compared with wild type chordomas. T98G is used as a positive control and U87MG is used as a negative control for PTEN expression. This is a representative blot from three independent experiments. (B)Cell proliferation assay assessed by the MTS method demonstrating a higher rate of proliferation among chordoma cell lines with PTEN LOH compared with wild type. ** P<0.05, Two sample independent student’s t test. (C and D) Cell proliferation assay assessed by MTS method demonstrating a higher rate of proliferation for chordoma lines with PTEN LOH compared with wild type. Addition of 50ng/mL of PDGF results in increased proliferation in both PTEN LOH and wild type cells. Addition of 1 uM of PDGF inhibitor resulted in decreased proliferation compared to untreated control. **P<0.05, Two sample independent student’s t test compared to untreated control from respective cell lines. (E) A representative matrigel invasion assay from demonstrating significant decrease in invasion in response to PDGF inhibition among PTEN wild type chordoma lines compared with PTEN +/- cells. These images are representative of 3 independent experiments. *P<0.05, Two sample independent student’s t test.

History