Tyroservatide therapy for tumor invasion and metastasis of human ovarian carcinoma and colon carcinoma

被引:2
作者
Wang, Lanlan [1 ]
Che, Xuchun [1 ]
Li, Xueying [1 ]
Lv, Junqiang [1 ]
Zhou, Chunlei [1 ]
Wang, Song [1 ]
Zhu, Zhifeng [1 ]
Wang, Li [1 ]
Lin, Gang [3 ]
Lu, Rong [1 ,3 ]
Yao, Zhi [1 ,2 ]
机构
[1] Tianjin Med Univ, Dept Immunol, Tianjin 300070, Peoples R China
[2] Educ Minist China, Key Lab Immuno Microenvironm & Dis, Tianjin, Peoples R China
[3] Shenzhen Kangzhe Pharmaceut Co Ltd, Shenzhen, Guangdong, Peoples R China
关键词
adhesion; carcinoma; invasion; metalloproteinase; metastasis; peptide; proliferation; tyroservatide; MATRIX METALLOPROTEINASES; LUNG-CARCINOMA; BREAST-CANCER; CELLS; ANGIOGENESIS; GROWTH; GENE;
D O I
10.1097/CAD.0b013e328357bd31
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tyroservatide (YSV) is an active, low-molecular-weight peptide shown to have antimetastasic effects on experimental melanoma and lung carcinoma. This study was carried out to evaluate the therapeutic effects of YSV on tumor invasion and metastasis of ovarian carcinoma and colon carcinoma and explore its antitumor mechanism of action. In vivo, three metastasis models were established, and YSV inhibited abdominal cavity metastasis of human ovarian carcinoma, and liver metastasis after spleen implantation of human colon carcinoma, in mice. In vitro, YSV inhibited the proliferation, promoted the death of SKOV-3, HT-29, and SW620 cells, and inhibited the adhesion and invasion of these three types of cells. Through zymography, western blot, and reverse transcription-PCR methods, YSV was found to reduce the activity, expression, and mRNA level of matrix metalloproteinase (MMP)-2 and MMP-9. The results showed that YSV can inhibit tumor growth and metastasis of human ovarian carcinoma SKOV-3 and human colon carcinoma HT-29 and SW620. The mechanism of action of YSV may involve the inhibition of proliferation, promotion of death, inhibition of the adhesion and invasion of SKOV-3, HT-29, and SW620 cells by downregulating the expression and activity of MMP-2 and MMP-9. Anti-Cancer Drugs 23:1067-1077 (C) 2012 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:1067 / 1077
页数:11
相关论文
共 20 条
  • [1] Gene expression of angiogenic factors correlates with metastatic potential of prostate cancer cells
    Aalinkeel, R
    Nair, MPN
    Sufrin, G
    Mahajan, SA
    Chadha, KC
    Chawda, RP
    Schwartz, SA
    [J]. CANCER RESEARCH, 2004, 64 (15) : 5311 - 5321
  • [2] THE INTERACTION BETWEEN AROMATASE, METALLOPROTEINASE 2,9 AND CD44 IN BREAST CANCER
    Bagnoli, Fabio
    de Oliveira, Vilmar Marques
    Longo Galvao da Silva, Maria Antonieta
    Morrone Taromaru, Giuliana Cassia
    Rinaldi, Jose Francisco
    Aoki, Tsutomu
    [J]. REVISTA DA ASSOCIACAO MEDICA BRASILEIRA, 2010, 56 (04): : 472 - 477
  • [3] Che Xu-Chun, 2006, Ai Zheng, V25, P275
  • [4] Claudin-1 regulates cellular transformation and metastatic behavior in colon cancer
    Dhawan, P
    Singh, AB
    Deane, NG
    No, Y
    Shiou, SR
    Schmidt, C
    Neff, J
    Washington, MK
    Beauchamp, RD
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (07) : 1765 - 1776
  • [5] Rapid and simple comparison of messenger RNA levels using real-time PCR
    Dussault, AA
    Pouliot, M
    [J]. BIOLOGICAL PROCEDURES ONLINE, 2006, 8 (1) : 1 - 10
  • [6] Guang RJ, 2000, CANCER RES, V60, P749
  • [7] Inhibitory effects of progesterone on plasma membrane fluidity and tumorigenic potential of ovarian epithelial cancer cells
    McDonnel, AC
    Van Kirk, EA
    Isaak, DD
    Murdoch, WJ
    [J]. EXPERIMENTAL BIOLOGY AND MEDICINE, 2003, 228 (03) : 308 - 314
  • [8] Matrix metalloproteinases (MMP-2,9) and their tissue inhibitors (TIMP-1,2) as novel markers of stress response and atherogenesis in children with chronic kidney disease (CKD) on conservative treatment
    Musial, Kinga
    Zwolinska, Danuta
    [J]. CELL STRESS & CHAPERONES, 2011, 16 (01) : 97 - 103
  • [9] Anti-invasive and metastatic activities of evodiamine
    Ogasawara, M
    Matsunaga, T
    Takahashi, S
    Saiki, I
    Suzuki, H
    [J]. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2002, 25 (11) : 1491 - 1493
  • [10] Park BK, 2001, CANCER RES, V61, P7647