Effects of irradiation on bone invasion of breast cancer cells
Keywords:
bones, breast cancer, carbon, radiotherapy, periostinAbstract
Background: Periostin is overexpressed in metastases from bone cancer. Many studies have indicated that periostin plays an important role in bone metastasis. Radiotherapy improves local tumor control, but recent evidence suggests that irradiation of the target tumor can promote tumor invasion and metastasis. Objective: The purpose of the study was to examine the effects of irradiation with carbon ion or gamma ray on the expression of periostin in breast cancer cells and the cytokine levels of osteoblasts in bone tumor metastases. Materials and methods: Breast cancer cells (FM3A/R cells) were exposed to carbon ion or gamma ray and then cocultured with non-irradiated osteoblastic MC3T3-E1 cells. Periostin expression in breast cancer cells and the levels of cytokines influencing bone invasion in osteoblastic cells were measured. Results: Periostin expression increased after irradiation with carbon ion or gamma ray. Carbon ion-irradiated cells expressed less periostin than did gamma ray-irradiated cells. Carbon ion irradiation stimulated low levels of periostin synthesis than gamma ray irradiation. The cytokines influencing bone invasion levels rose in tandem with the increase in periostin level. Conclusions: Carbon ion irradiation may reduce the production of bone-destroying cytokines and vascularization factors by osteoblasts in the microenvironment of cancer invasion in bone. A combination of carbon ion irradiation and a periostin inhibitor would improve treatment of bone metastatic breast cancer.
References
Mundy GR. Metastasis to bone: causes, consequences and therapeutic opportunities. Nat Rev Cancer. 2002;2:584-93.
Vicini FA, Kestin L, Huang R, Martinez A. Does local recurrence affect the rate of distant metastases and survival in patients with early-stage breast carcinoma treated with breast-conserving therapy? Cancer. 2003;97:910-9.
Barcellos-Hoff MH, Ravani SA. Irradiated mammary gland stroma promotes the expression of tumorigenic potential by unirradiated epithelial cells. Cancer Res. 2000;60:1254-60.
Bouchard G, Bouvette G, Therriault H, Bujold R, Saucier C, Paquette B. Pre-irradiation of mouse mammary gland stimulates cancer cell migration and development of lung metastases. Br J Cancer. 2013;109:1829-38.
Lemay R, Archambault M, Tremblay L, Bujold R, Lepage M, Paquette B. Irradiation of normal mouse tissue increases the invasiveness of mammary cancer cells. Int J Radiat Biol. 2011;87:472-82.
Karasawa K. Breast cancer. In: Tsujii H, Kamada T, Shirai T, Noda K, Tsuji H, Karasawa K, editors. Carbonion radiotherapy; principles, practices, and treatment planning 1st ed. Tokyo: Springer; 2014. p. 303-7.
Akamatsu H, Karasawa K, Omatsu T, Isobe Y, Ogata R, Koba Y. First experience of carbon-ion radiotherapy for early breast cancer. Jpn J Radiol. 2014;32:288-295.
Sato K, Uematsu M, Saito T, Tsuda H, Takeuchi H, Shigekawa T, et al. Efficacy of accelerated partial breast irradiation as a neoadjuvant treatment for patients with breast cancer: a pilot study. Surgery. 2006;139:617-23.
Chu GC, Chung LW. RANK-mediated signaling network and cancer metastasis. Cancer Metastasis Rev. 2014;33:497-509.
Che J, Shen WZ, Deng Y, Dai YH, Liao YD, Yuan XL, et al. Effects of lentivirus-mediated silencing of periostin on tumor microenvironment and bone metastasis via the integrin-signaling pathway in lung cancer. Life Sci. 2017;182:10-21.
Horiuchi K, Amizuka N, Takeshita S, Takamatsu H, Katsuura M, Ozawa H, et al. Identification and characterization of a novel protein, periostin, with restricted expression to periosteum and periodontal ligament and increased expression by transforming growth factor beta. J Bone Miner Res. 1999;14:1239-49.
Takeshita S, Kikuno R, Tezuka K, Amann E. Osteoblast-specific factor 2: cloning of a putative bone adhesion protein with homology with the insect protein fasciclin I. Biochem J. 1993;294:271-8.
Markwald RR, Norris RA, Moreno-Rodriguez R, Levine RA. Developmental basis of adult cardiovascular diseases: valvular heart diseases. Ann NY Acad Sci. 2010;1188:177-83.
Norris RA, Moreno-Rodriguez R, Hoffman S, Markwald RR. The many facets of the matricelluar protein periostin during cardiac development, remodelling, and pathophysiology. J Cell Commun Signal. 2009;3:275-86.
Srimawong P, Sawajiri M, Terato H, Maruyama K, Tanimoto K. Effects of carbon ion irradiation via periostin on breast cancer cell invasion of the microenvironment. J Radiol Radiat Ther. 2016;4:1060.
Iekushi K, Taniyama Y, Azuma J, Katsuragi N, Dosaka N, Sanada F, et al. Novel mechanisms of valsartan on the treatment of acute myocardial infarction through inhibition of the antiadhesion molecule periostin. Hypertension. 2007;49:1409-14.
Kim CJ, Isono T, Tambe Y, Chano T, Okabe H, Okada Y, et al. Role of alternative splicing of periostin in human bladder carcinogenesis. Int J Oncol. 2008;32:161-9.
Kim CJ, Yoshioka N, Tambe Y, Kushima R, Okada Y, Inoue H. Periostin is down-regulated in high grade human bladder cancers and suppresses in vitro cell invasiveness and in vivo metastasis of cancer cells. Int J Cancer. 2005;117:51-8.
Norris RA, Moreno-Rodriguez RA, Sugi Y, Hoffman S, Amos J, Hart MM, et al. Periostin regulates atrioventricular valve maturation. Dev Biol. 2008;316:200-13.
Katsuragi N, Morishita R, Nakamura N, Ochiai T, Taniyama Y, Hasegawa Y, et al. Periostin as a novel factor responsible for ventricular dilation. Circulation. 2004;110:1806-13.
Shimizu H, Sakamoto M, Sakamoto S. Bone resorption by isolated osteoclasts in living versus devitalized bone: differences in mode and extent and the effects of human recombinant tissue inhibitor of metalloproteinases. J Bone Miner Res. 1990;5:411-8.
Shimazaki M, Nakamura K, Kii I, Kashima T, Amizuka N, Li M, et al. Periostin is essential for cardiac healing after acute myocardial infarction. J Exp Med. 2008; 205: 295-303.
Shimazaki M, Kudo A. Impaired capsule formation of tumors in periostin-null mice. Biochem Biophys Res Commun. 008;367:736-42.
Siriwardena BS, Kudo Y, Ogawa I, Kitagawa M, Kitajima S, Hatano H, et al. Periostin is frequently overexpressed and enhances invasion and angiogenesis in oral cancer. Br J Cancer. 2006;95:1396-403.
Yang J, Mani SA, Donaher JL, Ramaswamy S, Itzykson RA, Come C, et al. Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis. Cell. 2004;117:927-39.
Puglisi F, Puppin C, Pegolo E, Andreetta C, Pascoletti G, D'Aurizio F, et al. Expression of periostin in human breast cancer. J Clin Pathol. 2008;61:494-8.
Zhang Y, Zhang G, Li J, Tao Q, Tang W. The expression analysis of periostin in human breast cancer. J Surg Res. 2010;160:102-6.
Zhu M, Fejzo MS, Anderson L, Dering J, Ginther C, Ramos L, et al. Periostin promotes ovarian cancer angiogenesis and metastasis. Gynecol Oncol. 2010;119:337-44.
Sawajiri M, Nomura Y, Bhawal UK, Nishikiori R, Okazaki M, Mizoe J, et al. Different effects of carbon ion and gamma-irradiation on expression of receptor activator of NF-kB ligand in MC3T3-E1 osteoblast cells. Bull Exp Biol Med. 2006;142:618-24.
Qian LW, Mizumoto K, Urashima T, Nagai E, Maehara N, Sato N, et al. Radiation-induced increase in invasive potential of human pancreatic cancer cells and its blockade by a matrix metalloproteinase inhibitor, CGS27023. Clin Cancer Res. 2002;8:1223-7.
Wild-Bode C, Weller M, Rimber A, Dichigans J, Wick W. Sublethal irradiation promotes migration and invasiveness of glioma cells: implications for radiotherapy of human glioblastoma. Cancer Res. 2001;61:2744-50.
Trinkaus M, Ooi WS, Amir E, Popovic S, Kalina M, Kahn H, et al. Examination of the mechanisms of osteolysis in patients with metastatic breast cancer. Oncol Re. 2009;21:1153-9.
Downloads
Published
How to Cite
Issue
Section
License
บทความที่ได้รับการตีพิมพ์เป็นลิขสิทธิ์ของวารสารมะเร็งวิวัฒน์
ข้อความที่ปรากฏในบทความแต่ละเรื่องในวารสารวิชาการเล่มนี้เป็นความคิดเห็นส่วนตัวของผู้เขียนแต่ละท่านไม่เกี่ยวข้องกับ และบุคคลากรท่านอื่น ๆ ใน สมาคมฯ แต่อย่างใด ความรับผิดชอบองค์ประกอบทั้งหมดของบทความแต่ละเรื่องเป็นของผู้เขียนแต่ละท่าน หากมีความผิดพลาดใดๆ ผู้เขียนแต่ละท่านจะรับผิดชอบบทความของตนเองแต่ผู้เดียว