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  • [PLoS One.] Evaluation of connectivity map-discovered celastrol as a radiosensitizing agent in a murine lung carcinoma model: Feasibility study of diffusion-weighted magnetic resonance imaging.

    원광의대/ 전홍영, 윤권하*

  • 출처
    PLoS One.
  • 등재일
    2017 May 23
  • 저널이슈번호
    12(5):e0178204. doi: 10.1371/journal.pone.0178204. eCollection 2017.
  • 내용

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    Abstract

     

    This study was designed to identify potential radiosensitizing (RS) agents for combined radio- and chemotherapy in a murine model of human lung carcinoma, and to evaluate the in vivo effect of the RS agents using diffusion-weighted magnetic resonance imaging (DW-MRI). Radioresistance-associated genes in A549 and H460 cells were isolated on the basis of their gene expression profiles. Celastrol was selected as a candidate RS by using connectivity mapping, and its efficacy in lung cancer radiotherapy was tested. Mice inoculated with A549 carcinoma cells were treated with single ionizing radiation (SIR), single celastrol (SC), or celastrol-combined ionizing radiation (CCIR). Changes in radiosensitization over time were assessed using DW-MRI before and at 3, 6, and 12 days after therapy initiation. The tumors were stained with hematoxylin and eosin at 6 and 12 days after therapy. The percentage change in the apparent diffusion coefficient (ADC) value in the CCIR group was significantly higher than that in the SC and SIR group on the 12th day (Mann-Whitney U-test, p = 0.05; Kruskal-Wallis test, p < 0.05). A significant correlation (Spearman's rho correlation coefficient of 0.713, p = 0.001) was observed between the mean percentage tumor necrotic area and the mean ADC values after therapy initiation. These results suggest that the novel radiosensitizing agent celastrol has therapeutic effects when combined with ionizing radiation (IR), thereby maximizing the therapeutic effect of radiation in non-small cell lung carcinoma. In addition, DW-MRI is a useful noninvasive tool to monitor the effects of RS agents by assessing cellularity changes and sequential therapeutic responses. 

     

    Author information

    Jun HY1, Kim TH1, Choi JW2, Lee YH3, Lee KK4, Yoon KH1,3.​

    1Imaging Science Research Center, Wonkwang University Hospital, Iksan, Republic of Korea.2Laboratory of Pharmacogenetics, Kyung Hee University College of Pharmacy, Seoul, Republic of Korea.3Department of Radiology, Wonkwang University School of Medicine, Iksan, Republic of Korea.4Department of Radiation Oncology, Wonkwang University School of Medicine, Iksan, Republic of Korea. 

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