DIFFERENCES BETWEEN MAN AND MICE WITH RESPECT TO REPAIR KINETICS OF RADIATION-INDUCED DNA LESIONS, AFTER EXPOSURE TO BIOLOGICALLY RELEVANT DOSES OF X-RAYS

Author(s):  
A.A.W.M. van Loon ◽  
G.P. van der Schans ◽  
P.H.M. Lohman
2020 ◽  
Vol 21 (21) ◽  
pp. 8151
Author(s):  
Sharda Kumari ◽  
Shibani Mukherjee ◽  
Debapriya Sinha ◽  
Salim Abdisalaam ◽  
Sunil Krishnan ◽  
...  

Radiation therapy (RT), an integral component of curative treatment for many malignancies, can be administered via an increasing array of techniques. In this review, we summarize the properties and application of different types of RT, specifically, conventional therapy with x-rays, stereotactic body RT, and proton and carbon particle therapies. We highlight how low-linear energy transfer (LET) radiation induces simple DNA lesions that are efficiently repaired by cells, whereas high-LET radiation causes complex DNA lesions that are difficult to repair and that ultimately enhance cancer cell killing. Additionally, we discuss the immunogenicity of radiation-induced tumor death, elucidate the molecular mechanisms by which radiation mounts innate and adaptive immune responses and explore strategies by which we can increase the efficacy of these mechanisms. Understanding the mechanisms by which RT modulates immune signaling and the key players involved in modulating the RT-mediated immune response will help to improve therapeutic efficacy and to identify novel immunomodulatory drugs that will benefit cancer patients undergoing targeted RT.


1995 ◽  
Vol 7 (2) ◽  
pp. 181-217 ◽  
Author(s):  
Marie-Florence Grenier-Loustalot ◽  
Vincent Denizot ◽  
Daniel Beziers

In the context of radiation-induced polymerization of bismaleimide monomers, we have investigated the polymerization mechanisms and kinetics of a bismaleimide/vinyl-pyrrolidone system. Several parameters were considered, including the type of dose (electrons or x-rays), power, presence of a catalyst and the carbon fibre filler. To this end, we developed a methodology based on physicochemical studies by infrared absorption spectroscopy and solid state 3CNMR (CP-MAS) in order to quantify the chemical species created or residuals in the cross-linked network. The results (progression of the reaction and structure of the network formed) were correlated with thermal behaviour and compared with those obtained by thermal polymerization. Using an optimized formulation, we determined the thermal and mechanical properties of these radiation-polymerized prepolymers and composites.


2010 ◽  
Vol 173 (5) ◽  
pp. 645-650 ◽  
Author(s):  
Momoko Takahashi ◽  
Kaoru Takakura ◽  
Yoshiya Furusawa

1992 ◽  
Vol 13 (3) ◽  
pp. 457-462 ◽  
Author(s):  
A.A.W.M. van Loon ◽  
A.J. Timmerman ◽  
G.P. van der Schans ◽  
P.H.M. Lohman ◽  
R.A. Baan

2021 ◽  
Vol 22 (3) ◽  
pp. 1418
Author(s):  
Elham Shahhoseini ◽  
Masao Nakayama ◽  
Terrence J. Piva ◽  
Moshi Geso

This study examined the effects of gold nanoparticles (AuNPs) and/or ionizing radiation (IR) on the viability and motility of human primary colon epithelial (CCD841) and colorectal adenocarcinoma (SW48) cells as well as human primary epidermal melanocytes (HEM) and melanoma (MM418-C1) cells. AuNPs up to 4 mM had no effect on the viability of these cell lines. The viability of the cancer cells was ~60% following exposure to 5 Gy. Exposure to 5 Gy X-rays or 1 mM AuNPs showed the migration of the cancer cells ~85% that of untreated controls, while co-treatment with AuNPs and IR decreased migration to ~60%. In the non-cancerous cell lines gap closure was enhanced by ~15% following 1 mM AuNPs or 5 Gy treatment, while for co-treatment it was ~22% greater than that for the untreated controls. AuNPs had no effect on cell re-adhesion, while IR enhanced only the re-adhesion of the cancer cell lines but not their non-cancerous counterparts. The addition of AuNPs did not enhance cell adherence. This different reaction to AuNPs and IR in the cancer and normal cells can be attributed to radiation-induced adhesiveness and metabolic differences between tumour cells and their non-cancerous counterparts.


Molecules ◽  
2021 ◽  
Vol 26 (6) ◽  
pp. 1676
Author(s):  
Giulia Rossi ◽  
Martina Placidi ◽  
Chiara Castellini ◽  
Francesco Rea ◽  
Settimio D'Andrea ◽  
...  

Infertility is a potential side effect of radiotherapy and significantly affects the quality of life for adolescent cancer survivors. Very few studies have addressed in pubertal models the mechanistic events that could be targeted to provide protection from gonadotoxicity and data on potential radioprotective treatments in this peculiar period of life are elusive. In this study, we utilized an in vitro model of the mouse pubertal testis to investigate the efficacy of crocetin to counteract ionizing radiation (IR)-induced injury and potential underlying mechanisms. Present experiments provide evidence that exposure of testis fragments from pubertal mice to 2 Gy X-rays induced extensive structural and cellular damage associated with overexpression of PARP1, PCNA, SOD2 and HuR and decreased levels of SIRT1 and catalase. A twenty-four hr exposure to 50 μM crocetin pre- and post-IR significantly reduced testis injury and modulated the response to DNA damage and oxidative stress. Nevertheless, crocetin treatment did not counteract the radiation-induced changes in the expression of SIRT1, p62 and LC3II. These results increase the knowledge of mechanisms underlying radiation damage in pubertal testis and establish the use of crocetin as a fertoprotective agent against IR deleterious effects in pubertal period.


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