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5-Fluorouracil as a Tumor-Treating Field-Sensitizer in Colon Cancer Therapy.
Lee, Yeon-Joo; Cho, Jae-Min; Sai, Sei; Oh, Ju Yeon; Park, Ji-Ae; Oh, Se Jong; Park, Misun; Kwon, Junhye; Shin, Ui Sup; Beak, Jeong-Hwa; Lim, Sun Ha; Song, Jie-Young; Hwang, Sang-Gu; Kim, Eun Ho.
Afiliação
  • Lee YJ; Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Cho JM; Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Sai S; Department of Basic Medical Sciences for Radiation Damages, National Institute of Radiological Sciences, Chiba 263-8555, Japan.
  • Oh JY; Laboratory of Biochemistry, School of Life Sciences and Biotechnology, Korea University, Anam-ro 145, Seongbuk-gu, Seoul 136-701, Korea.
  • Park JA; Division of Applied RI, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Oh SJ; Division of Applied RI, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Park M; Department of Radiological & Clinical Research, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Kwon J; Department of Radiological & Clinical Research, Korea Cancer Center Hospital, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Shin US; Department of Surgery, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Beak JH; Radiation Biology Research Team, Research Center, Dongnam Institute of Radiological and Medical Sciences, Busan 46033, Korea.
  • Lim SH; Department of Biochemistry, School of Medicine, Daegu Catholic University, 33, 17-gil, Duryugongwon-ro, Nam-gu, Daegu 42472, Korea.
  • Song JY; Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Hwang SG; Division of Radiation Biomedical Research, Korea Institute of Radiological and Medical Sciences, Seoul 01812, Korea.
  • Kim EH; Department of Biochemistry, School of Medicine, Daegu Catholic University, 33, 17-gil, Duryugongwon-ro, Nam-gu, Daegu 42472, Korea.
Cancers (Basel) ; 11(12)2019 Dec 12.
Article em En | MEDLINE | ID: mdl-31842288
ABSTRACT
Colorectal cancer (CRC) is a major cause of mortality that can be treated effectively with chemotherapy and radiotherapy, although resistance to these therapeutic modalities often occurs. Tumor-treating fields (TTFields) can block tumor growth by selectively impairing tumor cell division. In this study, we investigated the mechanism by which 5-fluorouracil (5-FU) sensitizes tumor cells to TTFields. Human HCT116 and SW480 CRC cells were treated with 5-FU and/or TTFields, and characterized in vitro in terms of cell viability, apoptosis through reactive oxygen species production, autophagy, and metastatic potentials. The biological effects of 5-FU and/or TTFields were studied via positron emission tomography and computed tomography on xenograft tumor growth and were confirmed with organoid models of patients. Our results revealed that combination treatment with 5-FU and TTFields increased the efficiency of TTFields therapy in colon cancer cells by downregulating signaling pathways associated with cell proliferation, survival, cell invasion, and migration while upregulating pathways mediating apoptosis and autophagic cell death. The novel mechanistic insights gleaned in this study suggest that combination therapy with TTFields and 5-FU may be effective in treating CRC, although safety and efficacy testing in patients with CRC will need to be performed before this strategy can be implemented clinically for TTF-sensitization.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cancers (Basel) Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cancers (Basel) Ano de publicação: 2019 Tipo de documento: Article