Gene therapy enhances the antiproliferative effect of radiation in intimal hyperplasia

被引:6
作者
Fortunato, JE
Mauceri, HJ
Kocharyan, H
Song, RH
Salloum, R
Vosicky, J
Swedberg, K
Malik, S
Abusharif, F
Glagov, S
Weichselbaum, RR
Bassiouny, HS
机构
[1] Univ Chicago, Dept Surg, Vasc Surg Sect, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Radiat & Cellular Oncol, Chicago, IL 60637 USA
关键词
ionizing radiation; intimal hyperplasia; vascular smooth muscle cells; right common carotid artery; cytosine deaminase; 5-fluorocytosine; 5-fluorouracil; intimal/medial; proliferating cell nuclear antigen;
D O I
10.1006/jsre.2000.5814
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Although ionizing radiation (IR) has been demonstrated to attenuate vessel wall restenosis and intimal hyperplasia (IH), dose-related mural injury and atrophy are possible deleterious side effects. We tested the hypothesis that a radiosensitizing strategy may improve IR-induced inhibition of in vivo vascular smooth muscle cells (VSMCs) without influencing apoptotic cell death. Methods. In 28 New Zealand White rabbits, the right common carotid artery (CCA) was injured and subjected to low-flow conditions to promote IH. The CCA was transfected with an adenoviral vector incorporating the cytosine deaminase (CD) gene (1 x 10(9) PFU/ml). 5-Fluorocytosine (5-FC), a prodrug that is converted to the radiosensitizing agent 5-fluorouracil (5-FU) by CD, was thereafter administered intravenously, The CCA was exposed to 5 Gy IR at 24 h. Intimal/medial (I/M) area and thickness ratios were determined in the harvested CCAs at 14 days. VSMC proliferative and apoptotic indices were assessed with immunohistochemistry. Results. A 50% reduction in UM area was found in rabbits treated with IR and IR + CD/5-FC (0.19 +/- 0.03 and 0.18 +/- 0.02) when compared with untreated controls (UC) (0.37 +/- 0.06) (P = 0.005). This finding was substantiated by attenuation of I/M thickness in the LR groups [0.47 +/- 0.13 (IR), 0.41 +/- 0.11 (IR + CD/5-FC), 0.61 +/- 0.17 (UC)] (P = 0.007). The number of proliferating VSMCs was notably smaller when IR was combined with CD/5-FC (4.17 +/- 1.16 vs 2.97 +/- 1.09 log transformed cells/mm(2), P < 0.07). Apoptosis was similar in all groups. Conclusions. Both IR alone and IR combined with a radiosensitizing agent are effective in attenuating experimental IH. However, combination therapy is synergistic and achieves greater inhibition of VSMC proliferation and may involve selective killing of radioresistant S-phase VSMCs, IR + CD/5-FC represents a novel therapeutic strategy that offers potential for long-term control of IH. (C) 2000 Academic Press.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 37 条
[1]  
Bassiouny H, 1998, DEV CARDIOVASC MED, P3
[2]   ANASTOMOTIC INTIMAL HYPERPLASIA - MECHANICAL INJURY OR FLOW INDUCED [J].
BASSIOUNY, HS ;
WHITE, S ;
GLAGOV, S ;
CHOI, E ;
GIDDENS, DP ;
ZARINS, CK .
JOURNAL OF VASCULAR SURGERY, 1992, 15 (04) :708-717
[3]  
BASSIOUNY HS, 1988, ARTERIOSCLEROSIS, V8, pA617
[4]  
BASSIOUNY HS, 1988, CIRCULATION, V7, P394
[5]   STEADY FLOW IN A MODEL OF THE HUMAN CAROTID BIFURCATION .1. FLOW VISUALIZATION [J].
BHARADVAJ, BK ;
MABON, RF ;
GIDDENS, DP .
JOURNAL OF BIOMECHANICS, 1982, 15 (05) :349-362
[6]   PATHOBIOLOGY OF INTIMAL HYPERPLASIA [J].
DAVIES, MG ;
HAGEN, PO .
BRITISH JOURNAL OF SURGERY, 1994, 81 (09) :1254-1269
[7]   PHARMACOLOGICAL PREVENTION OF RESTENOSIS AFTER CORONARY ANGIOPLASTY - REVIEW OF THE RANDOMIZED CLINICAL-TRIALS [J].
FRANKLIN, SM ;
FAXON, DP .
CORONARY ARTERY DISEASE, 1993, 4 (03) :232-242
[8]   APOPTOSIS - A DIFFERENT TYPE OF CELL-DEATH [J].
GERSCHENSON, LE ;
ROTELLO, RJ .
FASEB JOURNAL, 1992, 6 (07) :2450-2455
[9]   INTIMAL HYPERPLASIA, VASCULAR MODELING, AND THE RESTENOSIS PROBLEM [J].
GLAGOV, S .
CIRCULATION, 1994, 89 (06) :2888-2891
[10]  
GLAGOV S, 1995, J VASC INVEST, V1, P2