4.1 Article

The different radiation response and radiation-induced bystander effects in colorectal carcinoma cells differing in p53 status

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.mrfmmm.2015.06.003

关键词

Radiation-induced bystander effect; Colon carcinoma cells differing in TP53 status; Apoptosis; Premature senescence; Pro-inflammatory cytokines IL-6 and IL-8; NF kappa B pathway

资金

  1. National Center of Science (Poland) [DEC-2012/05/B/ST6/03472]
  2. European Social Fund [UDA-POKL.04.01.01-00-072/09-00]
  3. [POIG.02.03.01-24-099/13]

向作者/读者索取更多资源

Radiation-induced bystander effect, appearing as different biological changes in cells that are not directly exposed to ionizing radiation but are under the influence of molecular signals secreted by irradiated neighbors, have recently attracted considerable interest due to their possible implication for radiotherapy. However, various cells present diverse radiosensitivity and bystander responses that depend, inter alia, on genetic status including TP53, the gene controlling the cell cycle, DNA repair and apoptosis. Here we compared the ionizing radiation and bystander responses of human colorectal carcinoma HCf 116 cells with wild type or knockout TP53 using a transwell co-culture system. The viability of exposed to X-rays (0-8 Gy) and bystander cells of both lines showed a roughly comparable decline with increasing dose. The frequency of micronuclei was also comparable at lower doses but at higher increased considerably, especially in bystander TP53-/- cells. Moreover, the TP53-/- cells showed a significantly elevated frequency of apoptosis, while TP53+/+ counterparts expressed high level of senescence. The cross-matched experiments where irradiated cells of one line were co-cultured with non-irradiated cells of opposite line show that both cell lines were also able to induce bystander effects in their counterparts, however different endpoints revealed with different strength. Potential mediators of bystander effects, IL-6 and IL-8, were also generated differently in both lines. The knockout cells secreted IL-6 at lower doses whereas wild type cells only at higher doses. Secretion of IL-8 by TP53-/- control cells was many times lower than that by TP53+/+ but increased significantly after irradiation. Transcription of the NF kappa BIA was induced in irradiated TP53+/+ mainly, but in bystanders a higher level was observed in TP53-/- cells, suggesting that TP53 is required for induction of NF kappa B pathway after irradiation but another mechanism of activation must operate in bystander cells. (C) 2015 Elsevier B.V. All rights reserved.

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