Guanine nucleotide‐binding protein 1 is one of the key molecules contributing to cancer cell radioresistance. Issue 10 (29th September 2014)

• Record Type: Journal Article
• Authors: Fukumoto, Motoi; Amanuma, Tatsuya; Kuwahara, Yoshikazu; Shimura, Tsutomu; Suzuki, Masatoshi; Mori, Shiro; Kumamoto, Hiroyuki; Saito, Yohei; Ohkubo, Yasuhito; Duan, Zhenfeng; Sano, Kenji; Oguchi, Tomohiro; Kainuma, Kazuyuki; Usami, Shinichi; Kinoshita, Kengo; Lee, Inchul; Fukumoto, Manabu
• Is Part Of: Cancer science. Volume 105:Issue 10(2014:Oct.)
• Page Start: 1351
• Page End: 1359
• Publication Date: 2014-09-29
• Subjects: Cancer -- Periodicals; Neoplasms -- Periodicals; Research -- Periodicals; Electronic journals; 616.994005
• DOI: 10.1111/cas.12489
• Languages: English
• ISSNs: 1347-9032

Abstract

<abstract abstract-type="main" id="cas12489-abs-0001"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Standard fractionated radiotherapy for the treatment of cancer consists of daily irradiation of 2‐Gy X‐rays, 5 days a week for 5–8 weeks. To understand the characteristics of radioresistant cancer cells and to develop more effective radiotherapy, we established a series of novel, clinically relevant radioresistant (CRR) cells that continue to proliferate with 2‐Gy X‐ray exposure every 24 h for more than 30 days <italic>in vitro</italic>. We studied three human and one murine cell line, and their CRR derivatives. Guanine nucleotide‐binding protein 1 (<italic>GBP1</italic>) gene expression was higher in all CRR cells than their corresponding parental cells. <italic>GBP1</italic> knockdown by siRNA cancelled radioresistance of CRR cells <italic>in vitro</italic> and in xenotransplanted tumor tissues in nude mice. The clinical relevance of GBP1 was immunohistochemically assessed in 45 cases of head and neck cancer tissues. Patients with GBP1‐positive cancer tended to show poorer response to radiotherapy. We recently reported that low dose long‐term fractionated radiation concentrates cancer stem cells (CSCs). Immunofluorescence staining of GBP1 was stronger in CRR cells than in corresponding parental cells. The frequency of Oct4‐positive CSCs was higher in CRR cells than in parental cells, however, was not as common as GBP1‐positive cells. GBP1‐positive cells were radioresistant, but radioresistant cells were not necessarily CSCs. We concluded that GBP1 overexpression is necessary for the radioresistant phenotype in CRR cells, and that targeting GBP1‐positive cancer cells is a more efficient method in conquering cancer than targeting CSCs.</p> </abstract>