| Literature DB >> 29448860 |
Jian Zhang1,2, Xinyu Qiu1,2, Kedi Xi1,2, Wentao Hu1,2, Hailong Pei1,2, Jing Nie1,2, Ziyang Wang1,2, Jiahan Ding1,2, Peng Shang1,2,3,4, Bingyan Li1, Guangming Zhou1,2.
Abstract
Radiation therapy is one of the routine treatment modalities for cancer patients. Ionizing radiation (IR) can induce bone loss, and consequently increases the risk of fractures with delayed and nonunion of the bone in the cancer patients who receive radiotherapy. The orchestrated bone remodeling can be disrupted due to the affected behaviors of bone cells, including bone mesenchymal stem cells (BMSCs), osteoblasts and osteoclasts. BMSCs and osteoblasts are relatively radioresistant compared with osteoclasts and its progenitors. Owing to different radiosensitivities of bone cells, unbalanced bone remodeling caused by IR is closely associated with the dose absorbed. For doses less than 2 Gy, osteoclastogenesis and adipogenesis by BMSCs are enhanced, while there are limited effects on osteoblasts. High doses (>10 Gy) induce disrupted architecture of bone, which is usually related to decreased osteogenic potential. In this review, studies elucidating the biological effects of IR on bone cells (BMSCs, osteoblasts and osteoclasts) are summarized. Several potential preventions and therapies are also proposed.Entities:
Keywords: Bone loss; bone mesenchymal stem cells; osteoblasts; osteoclasts; radiotherapy
Mesh:
Year: 2018 PMID: 29448860 DOI: 10.1080/03008207.2018.1439482
Source DB: PubMed Journal: Connect Tissue Res ISSN: 0300-8207 Impact factor: 3.417