| Literature DB >> 28252222 |
Nicola Alessio1, Giuseppe Esposito2,3, Giovanni Galano4, Roberto De Rosa5, Pasquale Anello2, Gianfranco Peluso6, Maria Antonella Tabocchini2,3, Umberto Galderisi1,6,7.
Abstract
The use of high-linear energy transfer charged particles is gaining attention as a medical tool because of the emission of radiations with an efficient cell-killing ability. Considerable interest has developed in the use of targeted alpha-particle therapy for the treatment of micrometastases. Moreover, the use of helium beams is gaining momentum, especially for treating pediatric tumors. We analyzed the effects of alpha particles on bone marrow mesenchymal stromal cells (MSCs), which have a subpopulation of stem cells capable of generating adipocytes, chondrocytes, and osteocytes. Further, these cells contribute toward maintenance of homeostasis in the body. MSCs were irradiated with low and high doses of alpha particles or X-rays and a comparative biological analysis was performed. At a low dose (40 mGy), alpha particles exhibited a limited negative effect on the biology of MSCs compared with X-rays. No significant perturbation of cell cycle was observed, and a minimal increase in apoptosis or senescence was detected. Self-renewal was preserved as revealed by the CFU assay. On the contrary, with 2000 mGy alpha particles, we observed adverse effects on the vitality, functionality, and stemness of MSCs. These results are the consequence of different proportion of cells targeted by alpha particles or X-rays and the quality of induced DNA damage. The present study suggests that radiotherapy with alpha particles may spare healthy stem cells more efficaciously than X-ray treatments, an observation that should be taken into consideration by physicians while planning irradiation of tumor areas close to stem cell niches, such as bone marrow. J. Cell. Biochem. 118: 2993-3002, 2017.Entities:
Keywords: APOPTOSIS; CANCER THERAPY; IRRADIATION; MESENCHYMAL STROMAL CELLS; SENESCENCE
Mesh:
Year: 2017 PMID: 28252222 DOI: 10.1002/jcb.25961
Source DB: PubMed Journal: J Cell Biochem ISSN: 0730-2312 Impact factor: 4.429