Hangeshashinto (TJ-14) prevents radiation-induced mucositis by suppressing cyclooxygenase-2 expression and chemotaxis of inflammatory cells

被引:17
|
作者
Kamide, D. [1 ]
Yamashita, T. [1 ,2 ]
Araki, K. [1 ]
Tomifuji, M. [1 ]
Shiotani, A. [1 ]
机构
[1] Natl Def Med Coll, Dept Otolaryngol Head & Neck Surg, Tokorozawa, Saitama 3598513, Japan
[2] Kitasato Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Sagamihara, Kanagawa 2520374, Japan
来源
CLINICAL & TRANSLATIONAL ONCOLOGY | 2017年 / 19卷 / 11期
关键词
Radiotherapy; Radiation-induced mucositis; Kampo; Supportive care; Cancer treatment; Inflammation; INDUCED ORAL MUCOSITIS; COX-2; EXPRESSION; CHEMOTHERAPY; CANCER; RADIOTHERAPY; HEAD; SEVERITY; IMPROVES;
D O I
10.1007/s12094-017-1672-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Radiation-induced oral mucositis is the most common side effect of radiotherapy in head and neck cancer; however, effective modalities for its prevention have not been established. In this study, we evaluated the effectiveness of Hangeshashinto (TJ-14), a Japanese herbal medicine, for preventing radiation-induced mucositis and elucidated its effect on inflammatory responses, including inflammatory cell chemotaxis and cyclooxygenase-2 (COX2) expression, in an animal model. Methods Syrian hamsters, 8-9 weeks old, were enrolled in this study. Animals were irradiated with a single 40 Gy dose to the buccal mucosa. Hamsters freely received a treatment diet mixed with 2% TJ-14 or a normal diet daily. The therapeutic effect was determined based on the visual mucositis score, body weight, and histological examination of infiltrated neutrophils and COX2 expression. Results TJ-14 significantly reduced the severity of mucositis. The percentage with severe mucositis (score >= 3) was 100% in the untreated group and 16.7% in the TJ-14 group (P < 0.05). There was no difference in body weight change between the groups; however, weight gain in the untreated group tended to be suppressed compared to that in the TJ-14 group during the peak period of mucositis. In addition, TJ-14 inhibited the infiltration of neutrophils and COX2 expression in irradiated mucosa (P < 0.05). Conclusions TJ-14 reduced the severity of mucositis in an animal model by suppressing the inflammatory response. Because TJ-14 is inexpensive and its safety is established, it is a promising candidate for the standard treatment of radiation-induced mucositis in cancer patients.
引用
收藏
页码:1329 / 1336
页数:8
相关论文
共 50 条
  • [31] Double-blind, placebo-controlled, randomized phase II study of TJ-14 (Hangeshashinto) for infusional fluorinated-pyrimidine-based colorectal cancer chemotherapy-induced oral mucositis
    Matsuda, Chu
    Munemoto, Yoshinori
    Mishima, Hideyuki
    Nagata, Naoki
    Oshiro, Mitsuru
    Kataoka, Masato
    Sakamoto, Junichi
    Aoyama, Toru
    Morita, Satoshi
    Kono, Toru
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2015, 76 (01) : 97 - 103
  • [32] Targeting cyclooxygenase-2 and oxidant stress pathways for attenuation of radiation-induced vascular dysfunction
    Ullm, S.
    Sehn, F.
    Laube, M.
    Tondera, C.
    Bechmann, N.
    Mosch, B.
    Kniess, T.
    Pietzsch, J.
    PROCEEDINGS OF THE 6TH EUROPEAN CONGRESS OF PHARMACOLOGY, 2013, : 87 - 90
  • [33] Cyclooxygenase-2 expression on urothelial and inflammatory cells of cystoscopic biopsies and urine cytology
    Mohamed, Moussa M.
    Omran, Z.
    Nossier, M.
    Lotfy, A.
    Swellam, T.
    VIRCHOWS ARCHIV, 2009, 455 : 151 - 152
  • [34] MODULATION OF IONIZING RADIATION-INDUCED G2 ARREST BY CYCLOOXYGENASE-2 AND ITS INHIBITOR CELECOXIB
    Jun, Hyun Jung
    Kim, Young Mee
    Park, Soo Yeon
    Park, Ji Sun
    Lee, Eun Jung
    Choi, Shin Ae
    Pyo, Hongryull
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2009, 75 (01): : 225 - 234
  • [35] Cyclooxygenase-2 impairs treatment effects of radiotherapy for cervical cancer by inhibition of radiation-induced apoptosis
    Ishikawa, Hitoshi
    Ohno, Tatsuya
    Kato, Shingo
    Wakatsuki, Masaru
    Iwakawa, Mayumi
    Ohta, Toshie
    Imai, Takashi
    Mitsuhashi, Norio
    Noda, Shin-Ei
    Nakano, Takashi
    Tsujii, Hirohiko
    INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2006, 66 (05): : 1347 - 1355
  • [36] Cyclooxygenase-2 expression is associated with infiltration of inflammatory cells in oral and skin canine melanomas
    Silveira, Tatiany L.
    Veloso, Emerson S.
    Goncalves, Ivy N. N.
    Costa, Renato F.
    Rodrigues, Michele A.
    Cassali, Geovanni D.
    Del Puerto, Helen L.
    Pang, Lisa Y.
    Argyle, David J.
    Ferreira, Enio
    VETERINARY AND COMPARATIVE ONCOLOGY, 2020, 18 (04) : 727 - 738
  • [37] Lipopolysaccharide-induced Cyclooxygenase-2 Expression in Mouse Transformed Clara Cells
    Britt, Rodney D., Jr.
    Locy, Morgan L.
    Tipple, Trent E.
    Nelin, Leif D.
    Rogers, Lynette K.
    CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2012, 29 (1-2) : 213 - 222
  • [38] Bombesin induced cyclooxygenase-2 expression and differentiation in intestinal epithelial cells.
    Guo, YS
    Wen, XD
    Townsend, CM
    Hellmich, MR
    GASTROENTEROLOGY, 2000, 118 (04) : A548 - A548
  • [39] Stretch-induced cyclooxygenase-2 expression in bladder smooth muscle cells.
    Park, JM
    Freeman, MR
    Peters, CA
    Schnermann, JB
    Briggs, JP
    JOURNAL OF UROLOGY, 1998, 159 (05): : 19 - 19
  • [40] Deguelin-induced inhibition of cyclooxygenase-2 expression in human bronchial epithelial cells
    Lee, HY
    Suh, YA
    Kosmeder, JW
    Pezzuto, JM
    Hong, WK
    Kurie, JM
    CLINICAL CANCER RESEARCH, 2004, 10 (03) : 1074 - 1079