Advanced malignant melanoma responds to Prunus mume Sieb. Et Zucc (Ume) extract: Case report and in vitro study

被引:25
作者
Matsushita, Shigeto [1 ]
Tada, Ko-Ichi [1 ]
Kawahara, Ko-Ichi [2 ]
Kawai, Kazuhiro [1 ]
Hashiguchi, Teruto [2 ]
Maruyama, Ikuro [2 ]
Kanekura, Takuro [1 ]
机构
[1] Kagoshima Univ, Dept Dermatol, Field Sensory Organol, Grad Sch Med & Dent Sci, Kagoshima 8908520, Japan
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Lab & Vasc Med Cardiovasc & Resp Disorders A, Kagoshima 8908520, Japan
关键词
Japanese apricot; Prunus mume Sieb. Et Zucc; triterpenoid; malignant melanoma; JAPANESE APRICOT; INHIBITS GROWTH; CELLS; MK615; APOPTOSIS; VARIETY; RELEASE; KINASES; PROTEIN; AGENT;
D O I
10.3892/etm_00000089
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Malignant melanoma (MM) is an aggressive chemoresistant skin cancer characterized by rapid metastasis and a poor prognosis. Therefore, the development of innovative effective therapies is critical. MK615 is an extract from the Japanese apricot Prunus mime Sieb. Et Zucc (Ume). At a neutral pH, it contains natural chemical substances such as triterpenoids that exert anti-neoplastic effects in several types of cancers. We found that in patients with advanced MM, MK615 dramatically suppressed the cutaneous in-transit metastasis of the disease. Pre- and post-treatment comparison of tumors showed that the apoptotic index was significantly increased by MK615. In vitro studies, MTT assay, flow cytometric cell cycle analysis and immunofluorescence microscopy revealed that MK615 inhibited the growth of SK-MEL28 cells in a dose-dependent manner, increased the proportion of cells in sub-G1 phase and induced apoptosis. We further examined the expression of the receptor for advanced glycation end products (RAGE). RAGE is a multi-ligand receptor that binds to a novel cytokine, high mobility group box protein 1 (HMGB1), as well as advanced glycation end products. There is evidence that RAGE/HMGB1 interactions enhance cell invasion in MM. Here, we present Western blotting and immunofluorescence microscopy data indicating that MK615 inhibited the expression of RAGE in SK-MEL28 cells, and suppressed the release of HMGB1 by SK-MEL28 cells. Our findings suggest that MK615 may be a valuable tool for treating MM and other malignant tumors.
引用
收藏
页码:569 / 574
页数:6
相关论文
共 25 条
[1]
The "Prunus mume Sieb. et Zucc" (Ume) is a rich natural source of novel anti-cancer substance [J].
Adachi, Masakazu ;
Suzuki, Yoshihiko ;
Mizuta, Toshinobu ;
Osawa, Tatsushi ;
Adachi, Taro ;
Osaka, Kazuhisa ;
Suzuki, Keiji ;
Shiojima, Kenji ;
Arai, Yoko ;
Masuda, Kazuo ;
Uchiyama, Miwa ;
Oyamada, Takashi ;
Clerici, Mario .
INTERNATIONAL JOURNAL OF FOOD PROPERTIES, 2007, 10 (02) :375-384
[2]
INSITU END-LABELING DETECTS DNA STRAND BREAKS IN APOPTOSIS AND OTHER PHYSIOLOGICAL AND PATHOLOGICAL STATES [J].
ANSARI, B ;
COATES, PJ ;
GREENSTEIN, BD ;
HALL, PA .
JOURNAL OF PATHOLOGY, 1993, 170 (01) :1-8
[3]
Membrane cholesterol but not putative receptors mediates anandamide-induced hepatocyte apoptosis [J].
Biswas, KK ;
Sarker, KP ;
Abeyama, K ;
Kawahara, K ;
Iino, S ;
Otsubo, Y ;
Saigo, K ;
Izumi, H ;
Hashiguchi, T ;
Yamakuchi, M ;
Yamaji, K ;
Endo, R ;
Suzuki, K ;
Imaizumi, H ;
Maruyama, I .
HEPATOLOGY, 2003, 38 (05) :1167-1177
[4]
Centrosome maturation: Aurora lights the way to the poles [J].
Brittle, AL ;
Ohkura, H .
CURRENT BIOLOGY, 2005, 15 (21) :R880-R882
[5]
Roles of aurora kinases in mitosis and tumorigenesis [J].
Fu, Jingyan ;
Bian, Minglei ;
Jiang, Qing ;
Zhang, Chuanmao .
MOLECULAR CANCER RESEARCH, 2007, 5 (01) :1-10
[6]
Effects of the tumor inhibitory triterpenoid avicin G on cell integrity, cytokinesis, and protein ubiquitination in fission yeast [J].
Gutterman, JU ;
Lai, HT ;
Yang, PR ;
Haridas, V ;
Gaikwad, A ;
Marcus, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (36) :12771-12776
[7]
Focus on melanoma [J].
Houghton, AN ;
Polsky, D .
CANCER CELL, 2002, 2 (04) :275-278
[8]
HMGB1 expression by activated vascular smooth muscle cells in advanced human atherosclerosis plaques [J].
Inoue, Katsumi ;
Kawahara, Ko-ichi ;
Biswas, Karnal Krishna ;
Ando, Kenji ;
Mitsudo, Kazuaki ;
Nobuyoshi, Masakiyo ;
Maruyama, Ikuro .
CARDIOVASCULAR PATHOLOGY, 2007, 16 (03) :136-143
[9]
Proteolytic cleavage of high mobility group box 1 protein by thrombin - Thrombomodulin complexes [J].
Ito, Takashi ;
Kawahara, Ko-ichi ;
Okamoto, Kohji ;
Yamada, Shingo ;
Yasuda, Minetsugu ;
Imaizumi, Hitoshi ;
Nawa, Yuko ;
Meng, Xiaojie ;
Shrestha, Binita ;
Hashiguchi, Teruto ;
Maruyama, Ikuro .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (10) :1825-1830
[10]
HMGB1 release in co-cultures of porcine endothelial and human T cells [J].
Kawahara, Ko-Ichi ;
Setoyama, Kentaro ;
Kikuchi, Kiyoshi ;
Biswas, Kamal Krishna ;
Kamimura, Ryozo ;
Iwata, Masahiro ;
Ito, Takashi ;
Morimoto, Yoko ;
Hashiguchi, Teruto ;
Takao, Sonshin ;
Maruyama, Ikuro .
XENOTRANSPLANTATION, 2007, 14 (06) :636-641