CEA-related cell adhesion molecule-1 is involved in angiogenic switch in prostate cancer.
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CEA-related cell adhesion molecule-1 is involved in angiogenic switch in prostate cancer. / Tilki, D; Irmak, S; Oliveira-Ferrer, Leticia; Hauschild, J; Miethe, K; Atakaya, H; Hammerer, P; Friedrich, Martin; Schuch, G; Galalae, R; Stief, C G; Kilic, E; Huland, H; Ergun, S.
In: ONCOGENE, Vol. 25, No. 36, 36, 2006, p. 4965-4974.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - CEA-related cell adhesion molecule-1 is involved in angiogenic switch in prostate cancer.
AU - Tilki, D
AU - Irmak, S
AU - Oliveira-Ferrer, Leticia
AU - Hauschild, J
AU - Miethe, K
AU - Atakaya, H
AU - Hammerer, P
AU - Friedrich, Martin
AU - Schuch, G
AU - Galalae, R
AU - Stief, C G
AU - Kilic, E
AU - Huland, H
AU - Ergun, S
PY - 2006
Y1 - 2006
N2 - We demonstrate here that epithelial carcinoembryonic antigen (CEA)-related cell adhesion molecule-1 (CEACAM1) downregulation in prostate intraepithelial neoplasia (PIN) is inversely correlated with its upregulation in adjacent blood vessels. CEACAM1 silencing in prostate cancer cell line DU-145 via small interfering ribonucleic acid (siRNA) increased but its overexpression suppressed the expression of angiogenic/lymphangiogenic factors such as vascular endothelial growth factor (VEGF)-A, -C and -D, and angiogenic inhibitor collagen 18/endostatin. Furthermore, CEACAM1 overexpression in DU-145 cells increased but CEACAM1 silencing reduced angiopoietin-1 expression. Inverse relation was found for angiopoietin-2. Supernatant of CEACAM1-overexpressing DU-145 suppressed but that of CEACAM1-silenced increased the VEGF-induced endothelial tubes. Electron microscopically the majority of PIN-associated blood vessels was structurally destabilized exhibiting endothelial fenestration, trans- and inter-endothelial gaps. In some PIN areas, invasion of single tumor cells into the destabilized blood vessels was observed. These data show that disappearance of epithelial CEACAM1 in PIN is accompanied by its upregulation in adjacent vasculature which apparently correlates with vascular destabilization and increased vascularization of prostate cancer. Strategies to either conserve the epithelial CEACAM1 or to target endothelial CEACAM1 might be useful for an anti-angiogenic therapy of prostate cancer.
AB - We demonstrate here that epithelial carcinoembryonic antigen (CEA)-related cell adhesion molecule-1 (CEACAM1) downregulation in prostate intraepithelial neoplasia (PIN) is inversely correlated with its upregulation in adjacent blood vessels. CEACAM1 silencing in prostate cancer cell line DU-145 via small interfering ribonucleic acid (siRNA) increased but its overexpression suppressed the expression of angiogenic/lymphangiogenic factors such as vascular endothelial growth factor (VEGF)-A, -C and -D, and angiogenic inhibitor collagen 18/endostatin. Furthermore, CEACAM1 overexpression in DU-145 cells increased but CEACAM1 silencing reduced angiopoietin-1 expression. Inverse relation was found for angiopoietin-2. Supernatant of CEACAM1-overexpressing DU-145 suppressed but that of CEACAM1-silenced increased the VEGF-induced endothelial tubes. Electron microscopically the majority of PIN-associated blood vessels was structurally destabilized exhibiting endothelial fenestration, trans- and inter-endothelial gaps. In some PIN areas, invasion of single tumor cells into the destabilized blood vessels was observed. These data show that disappearance of epithelial CEACAM1 in PIN is accompanied by its upregulation in adjacent vasculature which apparently correlates with vascular destabilization and increased vascularization of prostate cancer. Strategies to either conserve the epithelial CEACAM1 or to target endothelial CEACAM1 might be useful for an anti-angiogenic therapy of prostate cancer.
M3 - SCORING: Zeitschriftenaufsatz
VL - 25
SP - 4965
EP - 4974
JO - ONCOGENE
JF - ONCOGENE
SN - 0950-9232
IS - 36
M1 - 36
ER -
