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      Enhanced Expression of IGFBP-3 Reduces Radiosensitivity and Is Associated with Poor Prognosis in Oral Squamous Cell Carcinoma

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          Abstract

          Insulin-like growth factor (IGF) binding protein-3 (IGFBP-3) modulates various cell functions through IGF-dependent or independent mechanisms. However, its biological roles in the radiosensitivity of oral squamous cell carcinoma (OSCC) remain largely unknown. The purpose of this study was to determine the clinical significance and molecular mechanisms of the association between IGFBP-3 and OSCC radiosensitivity. We performed an immunohistochemical analysis of IGFBP-3 in 52 OSCC specimens from patients treated with preoperative chemoradiotherapy and surgery (phase II study). Associations between IGFBP-3 expression and clinicopathological features were also evaluated. In addition, we examined the effects of IGFBP-3 on post-X-ray irradiation radiosensitivity and DNA damage in vitro. High IGFBP-3 expression was significantly correlated with poor chemoradiotherapy responses and prognosis. With IGFBP-3 knockdown, irradiated OSCC cells exhibited significantly higher radiosensitivity compared with that of control cells. Moreover, IGFBP-3 depletion in OSCC cells reduced phosphorylation of the DNA-dependent protein kinase catalytic subunit (DNA-PKcs), which is required for DNA double-strand break repair during non-homologous end joining. These findings indicate that IGFBP-3 may have a significant role in regulating DNA repair and is be a potential biomarker for predicting clinical response to radiotherapy and prognosis in OSCC.

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          Most cited references37

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          IGF binding proteins in cancer: mechanistic and clinical insights.

          The six members of the family of insulin-like growth factor (IGF) binding proteins (IGFBPs) were originally characterized as passive reservoirs of circulating IGFs, but they are now understood to have many actions beyond their endocrine role in IGF transport. IGFBPs also function in the pericellular and intracellular compartments to regulate cell growth and survival - they interact with many proteins, in addition to their canonical ligands IGF-I and IGF-II. Intranuclear roles of IGFBPs in transcriptional regulation, induction of apoptosis and DNA damage repair point to their intimate involvement in tumour development, progression and resistance to treatment. Tissue or circulating IGFBPs might also be useful as prognostic biomarkers.
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            Chromosomal stability and the DNA double-stranded break connection.

            Genome stability is of primary importance for the survival and proper functioning of all organisms. Double-stranded breaks in DNA are important threats to genome integrity because they can result in chromosomal aberrations that can affect, simultaneously, many genes, and lead to cell malfunctioning and cell death. These detrimental consequences are counteracted by two mechanistically distinct pathways of double-stranded break repair: homologous recombination and non-homologous end-joining. Recently, unexpected links between these double-stranded break-repair systems, and several human genome instability and cancer predisposition syndromes, have emerged. Now, interactions between both double-stranded break-repair pathways and other cellular processes, such as cell-cycle regulation and replication, are being unveiled.
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              Cellular Stress Responses in Radiotherapy

              Radiotherapy is one of the major cancer treatment strategies. Exposure to penetrating radiation causes cellular stress, directly or indirectly, due to the generation of reactive oxygen species, DNA damage, and subcellular organelle damage and autophagy. These radiation-induced damage responses cooperatively contribute to cancer cell death, but paradoxically, radiotherapy also causes the activation of damage-repair and survival signaling to alleviate radiation-induced cytotoxic effects in a small percentage of cancer cells, and these activations are responsible for tumor radio-resistance. The present study describes the molecular mechanisms responsible for radiation-induced cellular stress response and radioresistance, and the therapeutic approaches used to overcome radioresistance.
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                Author and article information

                Journal
                Cancers (Basel)
                Cancers (Basel)
                cancers
                Cancers
                MDPI
                2072-6694
                20 February 2020
                February 2020
                : 12
                : 2
                : 494
                Affiliations
                [1 ]Department of Oral and Maxillofacial Surgery, Faculty of Life Sciences, Kumamoto University, Kumamoto 860-8556, Japan; jsakata@ 123456kuh.kumamoto-u.ac.jp (J.S.); ryoshida@ 123456kumamoto-u.ac.jp (R.Y.); yu6600@ 123456kuh.kumamoto-u.ac.jp (Y.M.); karapote@ 123456kuh.kumamoto-u.ac.jp (K.K.); haritah1@ 123456aih-net.com (H.A.); hikarun@ 123456kuh.kumamoto-u.ac.jp (H.N.); tatsuro.yamamoto@ 123456jfcr.or.jp (T.Y.); nagatama0213@ 123456kuh.kumamoto-u.ac.jp (M.N.); idd09017m@ 123456kuh.kumamoto-u.ac.jp (S.K.); shun2707@ 123456kuh.kumamoto-u.ac.jp (S.G.); dd09034w@ 123456kuh.kumamoto-u.ac.jp (Y.N.); idd09053y@ 123456kuh.kumamoto-u.ac.jp (K.Y.)
                [2 ]Department of Radiation Oncology, Kumamoto University Hospital, Kumamoto 860-8556, Japan; ryo108@ 123456kumamoto-u.ac.jp
                [3 ]Department of Medical Imaging, Faculty of Life Sciences, Kumamoto University, Kumamoto 862-0976, Japan; murakami@ 123456kumamoto-u.ac.jp
                [4 ]Radiation Biology and Medicine, Faculty of Medicine, Tohoku Medical and Pharmaceutical University, 4-4-1, Komatsushima, Aoba, Sendai, Miyagi 981-8558, Japan; y-kuwahara@ 123456umin.ac.jp
                [5 ]Department of Molecular Pathology, Tokyo Medical University, 6-1-1, Shinjuku, Shinjuku, Tokyo 160-8402, Japan; manabu.fukumoto.a8@ 123456tohoku.ac.jp
                Author notes
                [* ]Correspondence: ahiro711@ 123456kumamoto-u.ac.jp (A.H.); hinakaya@ 123456kumamoto-u.ac.jp (H.N.); Tel.: +81-96-373-5288 (A.H. & H.N.)
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-5190-8663
                https://orcid.org/0000-0002-2701-6462
                https://orcid.org/0000-0002-2317-384X
                https://orcid.org/0000-0001-9764-5718
                https://orcid.org/0000-0002-3244-0268
                Article
                cancers-12-00494
                10.3390/cancers12020494
                7072421
                32093285
                e7ccbe2b-bb4d-4f88-8cb4-c131c754958b
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 15 January 2020
                : 18 February 2020
                Categories
                Article

                dna repair,igfbp-3,oral squamous cell carcinoma,dna-pkcs,radiosensitivity

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