Both high intratumoral microvessel density determined using CD105 antibody and elevated plasma levels of CD105 in colorectal cancer patients correlate with poor prognosis

被引:104
作者
Li, C
Gardy, R
Seon, B
Duff, S
Abdalla, S
Renehan, A
O'Dwyer, ST
Haboubi, N
Kumar, S [1 ]
机构
[1] Univ Manchester, Dept Pathol, Manchester, Lancs, England
[2] Trafford Gen Hosp, Dept Pathol, Manchester, Lancs, England
[3] Univ Toronto, Hosp Sick Children, Dept Immunol, Toronto, ON M5G 1X8, Canada
[4] Christie Hosp, Dept Surg, Manchester, Lancs, England
[5] Roswell Pk Canc Inst, Dept Mol Immunol, Buffalo, NY 14263 USA
关键词
angiogenesis; soluble CD105; microvessel density (MVD); TGF beta;
D O I
10.1038/sj.bjc.6600874
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
CD105 and its ligand transforming growth factor beta (TGFbeta) are modulators of angiogenesis, which drives tumour growth and metastasis. Tumour microvessel density (MVD) has proven to be an important determinant of prognosis. In this study, we have examined the prognostic value of MVD identified using Mabs to the pan-endothelial marker CD34 and to CID 105 in III patients with colorectal cancer. The Mab to CID 105 preferentially reacts with angiogenic endothelial cells. Of the III patients studied, 38 were alive and 73 had died of the disease. The median MVD values counted using anti-CD34 and anti-CD105 were 5 (range 1.40-9.00) and 3.10 (range 0.90-8.00), respectively. Kaplan-Meier survival analysis revealed that only MVD values obtained using CID 105 Mab correlated with survival. Patients with a high MVD, above the median (3.10), showed the worst prognosis. A similar outcome was observed when MVD was divided into quartiles. In order to ascertain if this strong expression of CD105 in the tumour vasculature is reflected in patients' plasma, circulating levels of CD105, TGFbeta1 and TGFbeta3 together with the receptor-ligand complexes were quantified in patients with colorectal carcinoma and normal controls. Results showed that except for TGFbeta1, the levels of all other molecules were significantly elevated compared with controls. The levels of CID 105 were positively correlated with Dukes' stages. A lower TGFbeta1 level was noted in patients with carcinoma over the controls. Furthermore, TGFbeta3 and CD105/TGFbeta3 complexes were markedly lowered in postoperative compared with preoperative plasma samples. Immunostaining revealed that TGFbeta1 was expressed in cancer cells but TGFbeta3 in the stromal cells, whereas CD105 was exclusively expressed in vascular endothelial cells of tumour blood vessels. In conclusion, this study demonstrates that MVD quantified using a Mab to CD105 is an independent prognostic parameter for survival of patients with colorectal cancer, and that plasma levels of CD105, TGFbeta1, TGFbeta3 and CD105/TGFbeta complexes may be useful markers for assessing disease progression. These data have led us to propose that quantification of these determinants may prove useful to monitor therapeutic efficacy in patients with colorectal cancer, especially those who are being treated with antiangiogenic therapies. (C) 2003 Cancer Research UK.
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页码:1424 / 1431
页数:8
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