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. 2011 Jul 1;5(4):332–343. doi: 10.4161/cam.5.4.17287

Table 2.

Characterization of MDA-MB-231 breast cancer cells overexpressing VEGF isoforms used in this study

(A) Clones number VEGF165 VEGF189 NRP1
cV 1 1 1
Clones V189 1.5 30.5# 1
V165 48# 1.4 1.4
(B) Clones number VEGF165 VEGF189 NRP1
shCtl 1 1 1
cV clones shNRP1–9 0.9 0.8 0.6*
shNRP1–19 0.5 0.5 0.4*
shCtl 1 1 1
V189 clones shNRP1–10 0.4* 9.7* 0.6*
shNRP1–11 0.48* 5.8* 0.57*
shCtl 1 1 1
V165 clones shNRP1–3 1 0.5 0.5*
shNRP1–5 0.7 0.6 0.4*

(A) VEGF overexpressing clones. Expression of VEGFmRNA was assessed using real-time PCR V189 clones (V189–13), V165 (V165–42) clones, and cV (cV-14) clones (for VEGF189 and VEGF165 overexpressing, or control clones, respectively), were initially described in reference 10; these clones were maintained in 10% SVF condition Data obtained using real-time PCR were expressed as mean values, as compared with cV clones set to 1. (B) ShNRP1 and shCtl transfected clones. Data, obtained in 10% FBS containing medium, were expressed as mean values of 4 independent experiments performed in duplicate, as compared with corresponding shCtl clone set to 1. Statistical significance (p < 0.05):

#

VEGF overexpressing vs. cV clone;

*

shNRP1 clone vs. shCtl clone.