Open AccessPreventive effects of 125I seeds on benign restenosis following esophageal stent implantation in a dog model
Author(s) -
Zhen Gan,
Jian Jing,
Guangyu Zhu,
Yuan Qin,
GaoJun Teng,
Jun Guo
Publication year - 2014
Publication title -
molecular medicine reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.727
H-Index - 56
eISSN - 1791-3004
pISSN - 1791-2997
DOI - 10.3892/mmr.2014.3130
Subject(s) - restenosis , apoptosis , cell cycle , fibroblast , esophageal cancer , cell growth , propidium iodide , cell , hyperplasia , pathology , medicine , annexin , oncogene , andrology , stent , staining , urology , cancer research , biology , cancer , programmed cell death , cell culture , biochemistry , genetics
The present study aimed to evaluate the effects of iodine‑125 (125I) seeds on the proliferation of primary esophageal fibroblasts in dogs, and to assess the safety and preventive efficacy of 125I seed‑pre‑loaded esophageal stents in benign restenosis following implantation. Primary fibroblasts were cultured with various 125I seed activities, which were then evaluated using cell proliferation and apoptosis assays as well as cell cycle analysis using Annexin V/propidium iodide (PI) double staining and PI staining. Prior to sacrification, animals were submitted to esophageal radiography under digital subtraction angiography. Esophageal tissues were collected and examined for macroscopic, microscopic and pathological alterations. The results demonstrated a significant and dose‑dependent inhibition of fibroblast proliferation and increased apoptosis following exposure to 125I seeds. G0/G1 fibroblast populations increased in a dose‑dependent manner following treatment with 125I seeds, in contrast to cells in S phase. Four weeks following implantation, α‑smooth muscle actin and proliferating cell nuclear antigen expression levels in the experimental group were significantly lower compared with those in the control group; in addition, eight weeks following implantation, esophageal inner diameters were increased in the experimental group. 125I seeds inhibited proliferation of dog esophageal fibroblasts via cell cycle arrest and apoptosis. In conclusion, 125I seed‑pre‑loaded esophageal stents inhibited benign hyperplasia in the upper edge of the stent to a certain extent, which relieved benign restenosis following implantation with a good safety profile.