Effects of Mesenchymal Stem Cells Treatment on Radiation-Induced Proctitis in Rats

There are no effective treatment methods with which to control complications of radiation proctitis with fistula or recurrent bleeding following radiation treatment for prostate, cervical, or rectal cancer. Mesenchymal stem cells (MSCs) can induce immune modification, resulting in tissue repair and...

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Published inYonsei medical journal Vol. 64; no. 3; pp. 167 - 174
Main Authors Kim, Won Hee, Yoo, Jun Hwan, Yoo, In Kyung, Kwon, Chang Il, Hong, Sung Pyo
Format Journal Article
LanguageEnglish
Published Korea (South) Yonsei University College of Medicine 01.03.2023
연세대학교의과대학
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ISSN0513-5796
1976-2437
1976-2437
DOI10.3349/ymj.2022.0342

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Summary:There are no effective treatment methods with which to control complications of radiation proctitis with fistula or recurrent bleeding following radiation treatment for prostate, cervical, or rectal cancer. Mesenchymal stem cells (MSCs) can induce immune modification, resulting in tissue repair and regeneration. Therefore, we used a rat model of radiation-induced proctitis and observed the effects of using human placenta-derived (PD) and adipose tissue-derived (AD) MSCs. Female Sprague Dawley rats were irradiated at the pelvic area with 25 Gy. We injected 1×10 cells of human PD-MSCs, human AD-MSCs, human foreskin fibroblasts, and control media into the rectal submucosa following irradiation. We sacrificed rats for pathologic evaluation. Fibrosis on the rectum was reduced in both MSC groups, compared to the control group. Mucosal Ki-67 indices of both MSC injected groups were higher than those in the control group. Although caspase-3 positive cells in the mucosa gradually increased and decreased in the control group, those in both MSC injected groups increased rapidly and decreased thereafter. We demonstrated the effects of regional MSC injection treatment for radiation-induced proctitis in rats. MSC injection reduced fibrosis and increased proliferation in rat mucosa. Human AD-MSCs and PD-MSCs had similar effectiveness.
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https://www.eymj.org/DOIx.php?id=10.3349/ymj.2022.0342
ISSN:0513-5796
1976-2437
1976-2437
DOI:10.3349/ymj.2022.0342