Platelet-derived growth factor (PDGF)-signaling mediates radiation-induced apoptosis in human prostate cancer cells with loss of p53 function

被引:16
作者
Kim, HE
Han, SJ
Kasza, T
Han, R
Choi, HS
Palmer, KC
Kim, HRC
机构
[1] WAYNE STATE UNIV,DEPT PATHOL,SCH MED,DETROIT,MI 48202
[2] WAYNE STATE UNIV,DEPT RADIAT ONCOL,SCH MED,DETROIT,MI 48202
[3] VET ADM MED CTR,DEPT RADIAT ONCOL,DETROIT,MI 48202
[4] EWHA WOMANS UNIV,DEPT BIOL,SEOUL,SOUTH KOREA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 1997年 / 39卷 / 03期
关键词
platelet-derived growth factor; radiation-induced apoptosis; human prostate cancer cells;
D O I
10.1016/S0360-3016(97)00358-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Platelet-derived growth factor (PDGF) signals a diversity of cellular responses irt vitro, including cell proliferation, survival, transformation, and chemotaxis. PDGF functions as a ''competence factor'' to induce a set of early response genes expressed in G(1) including p21(WAF1/CIP1), a functional mediator of the tumor suppressor gene p53 in G(1)/S checkpoint, For PDGF-stimulated cells to progress beyond G(1) and transit the cell cycle completely, progression factors in serum such as insulin and IGF-1 are required, We have recently shown a novel role of PDGF in inducing apoptosis in growth-arrested murine fibroblasts, The PDGF-induced apoptosis is rescued by insulin, suggesting that G(1)/S checkpoint is a critical determinant for PDGF-induced apoptosis, Because recent studies suggest that radiation-induced signal transduction pathways interact with growth factor-mediated signaling pathways, we have investigated whether activation of the PDGF-signaling facilitates the radiation-induced apoptosis in the absence of functional p53, For this study we have used the 125-IL cell line, a mutant p53-containing, highly metastatic, and hormone-unresponsive human prostate carcinoma cell line, PDGF signaling is constitutively activated by transfection with a p28(v-sis) expression vector, which was previously shown to activate PDGF alpha- and beta-receptors, Although the basal level of p21(WAF1/CIP1) expression and radiation-induced apoptosis were not detectable in control 125-IL cells as would be predicted in mutant p53-containing cells, activation off PDGF-signaling induced expression of p21(WAF1/CIP1) and radiation-induced apoptosis, Our study suggests that the level of ''competence'' growth factors including PDGF may be one of the critical determinants for radiation-induced apoptosis, especially in cells with loss of p53 function at the site of radiotherapy in vivo. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:731 / 736
页数:6
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