Lactobacillus rhamnosus GG induces tumor regression in mice bearing orthotopic bladder tumors

被引:64
作者
Seow, Shih Wee [1 ]
Cai, Shirong [1 ]
Rahmat, Juwita N. [1 ]
Bay, Boon Huat [2 ]
Lee, Yuan Kun [3 ]
Chan, Yiong Huak [4 ]
Mahendran, Ratha [1 ]
机构
[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Surg, Singapore 117595, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Anat, Singapore 117595, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Singapore 117595, Singapore
[4] Natl Univ Singapore, Yong Loo Lin Sch Med, Biostat Unit, Singapore 117595, Singapore
关键词
BACILLUS-CALMETTE-GUERIN; MYCOBACTERIUM-BOVIS; T-CELLS; NEUTROPHIL GRANULOCYTES; BCG IMMUNOTHERAPY; CASEI PREPARATION; MURINE BLADDER; XCR1; RECEPTOR; CANCER; MACROPHAGES;
D O I
10.1111/j.1349-7006.2009.01426.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present gold standard for bladder cancer is Mycobacterium bovis, Bacillus Calmette Guerin (BCG) immunotherapy. But it has a non-responder rate of 30-50% and side effects are common. Lactobacillus casei strain Shirota has been reported to reduce the incidence of recurrence in bladder cancer patients and to cure tumor-bearing mice. Our aim was to determine if Lactobacillus rhamnosus GG (LGG) could be as efficacious as BCG in a murine model of bladder cancer. MB49 bladder cancer cells secreting human prostate-specific antigen were implanted orthotopically in female C57BL/6 mice and urinary prostate-specific antigen levels were used as a marker of tumor growth. Mice were treated with either live or lyophilized LGG given via intravesical instillation, or both oral and intravesical LGG given once a week for a period of 6 weeks starting at day 4 after tumor implantation. A comparison of LGG and BCG immunotherapy was also carried out. LGG therapy (live or lyophilized) significantly (P = 0.006) increased the number of cured mice. Cytokine arrays and immune cell recruitment analysis revealed differences between untreated, treated, cured, and tumor-bearing mice. LGG therapy restored XCL1 levels to those in healthy bladders. LGG also recruited large numbers of neutrophils and macrophages to the tumor site. Intravesical LGG and BCG immunotherapy had cure rates of 89 and 77%, respectively, compared with 20% in untreated mice. LGG has the potential to replace BCG immunotherapy for the treatment of bladder cancer. (Cancer Sci 2010; 101: 751-758)
引用
收藏
页码:751 / 758
页数:8
相关论文
共 39 条
[1]   BCG immunotherapy of bladder cancer: 20 years on [J].
Alexandroff, AB ;
Jackson, AM ;
O'Donnell, MA ;
James, K .
LANCET, 1999, 353 (9165) :1689-1694
[2]  
Amling CL, 2001, CURR PROB CANCER, V25, P219
[3]   ANTITUMOR-ACTIVITY OF LACTOBACILLUS-CASEI (LC 9018) AGAINST EXPERIMENTAL MOUSE BLADDER-TUMOR (MBT-2) [J].
ASANO, M ;
KARASAWA, E ;
TAKAYAMA, T .
JOURNAL OF UROLOGY, 1986, 136 (03) :719-721
[4]   PROPHYLACTIC EFFECT OF A LACTOBACILLUS-CASEI PREPARATION ON THE RECURRENCE OF SUPERFICIAL BLADDER-CANCER [J].
ASO, Y ;
AKAZAN, H .
UROLOGIA INTERNATIONALIS, 1992, 49 (03) :125-129
[5]   PREVENTIVE EFFECT OF A LACTOBACILLUS-CASEI PREPARATION ON THE RECURRENCE OF SUPERFICIAL BLADDER-CANCER IN A DOUBLE-BLIND TRIAL [J].
ASO, Y ;
AKAZA, H ;
KOTAKE, T ;
TSUKAMOTO, T ;
IMAI, K ;
NAITO, S .
EUROPEAN UROLOGY, 1995, 27 (02) :104-109
[6]   Inhibitory effects of freeze-dried milk fermented by selected Lactobacillus bulgaricus strains on carcinogenesis induced by 1,2-dimethylhydrazine in rats and by diethylnitrosamine in hamsters [J].
Balansky, R ;
Gyosheva, B ;
Ganchev, G ;
Mircheva, Z ;
Minkova, S ;
Georgiev, G .
CANCER LETTERS, 1999, 147 (1-2) :125-137
[7]   Macrophages are vital in spontaneous intraocular tumor eradication [J].
Boonman, Zita F. H. M. ;
Schurmans, Lucas R. H. M. ;
van Rooijen, Nico ;
Melief, Cornelis J. M. ;
Toes, Rene E. M. ;
Jager, Martine J. .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (07) :2959-2965
[8]   Thirty years of BCG immunotherapy for non-muscle invasive bladder cancer: A success story with room for improvement [J].
Brandau, Sven ;
Suttmann, Henrik .
BIOMEDICINE & PHARMACOTHERAPY, 2007, 61 (06) :299-305
[9]   Lymphotactin expression by engineered myeloma cells drives tumor regression:: Mediation by CD4+ and CD8+ T cells and neutrophils expressing XCR1 receptor [J].
Cairns, CM ;
Gordon, JR ;
Li, F ;
Baca-Estrada, ME ;
Moyana, T ;
Xiang, J .
JOURNAL OF IMMUNOLOGY, 2001, 167 (01) :57-65
[10]   Correlation of osteopontin protein expression and pathological stage across a wide variety of tumor histologies [J].
Coppola, D ;
Szabo, M ;
Boulware, D ;
Muraca, P ;
Alsarraj, M ;
Chambers, AF ;
Yeatman, TJ .
CLINICAL CANCER RESEARCH, 2004, 10 (01) :184-190