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. Author manuscript; available in PMC: 2010 May 4.
Published in final edited form as: Angiogenesis. 2009 Feb 17;12(2):159–164. doi: 10.1007/s10456-009-9135-7

Table 1.

Summary of studies showing the extent of EPCs incorporation to the tumor vasculature

EPC
incorporation (%)
Type of tumor BM donor Markers used Reference
<0.01 B16 melanoma VEGFR-2/Lac-Z Lac-Z, CD31, CD105,
   von Willebrand factor
[14]
<0.01 GFP GFP, CD31 [17]
80–100 B6RV2 lymphoma Lac-Z Von Willebrand factor, Lac-Z [6]
<0.01 End-SCL-Cre-ERt Lac-Z, CD31 [13]
<0.01 Lewis lung carcinoma End-SCL-Cre-ERt Lac-Z, CD31 [13]
<0.01 GFP GFP, CD31 [17]
0.01–0.15 GFP GFP, CD31 [24]
0.02 Tie-2/GFP GFP, CD31 [12]
1–2 GFP Linc-kit+Sca-1+, GFP, CD31 [15]
50–100 Lac-Z Von Willebrand factor, Lac-Z [6]
50 MCA/129 fibrosarcoma Lac-Z Von Willebrand factor, Lac-Z [11]
7–10 MMTV-PyMT spontaneous
   mammary carcinoma
GFP CD31, VE-cadherin, GFP [5]
2.5–3.5 MT1A2 mouse mammary
   carcinoma
Tie2/Lac-Z Lac-Z, CD31 [17]
7–10 Namalwa lymphoma Human BM Human CD31, CD34, CD133 [74]
10–25 Spontaneous tumor
   (NOD/SCID/β-
   glucuronidase −/−)
NOD/SCID/β-glucuronidase β-Glucuronidase, VE-cadherin [29]
0.5 TG1-1 mouse mammary
   carcinoma
GFP GFP, CD133 [75]
<0.01 GFP GFP, CD31 [17]

The selected studies all used bone marrow transplantation followed at least 4 weeks later by tumor implantation. Models of parabiosis or ex vivo injection of EPCs were not included