Antitumor activity of photodynamic therapy with a chlorin derivative in vitro and in vivo

Tumor Biology ◽  
2015 ◽  
Vol 36 (9) ◽  
pp. 6839-6847 ◽  
Author(s):  
Lai-Xing Wang ◽  
Jian-Wei Li ◽  
Jian-Yue Huang ◽  
Jian-Hong Li ◽  
Li-Jun Zhang ◽  
...  
Neoplasma ◽  
2016 ◽  
Vol 63 (01) ◽  
pp. 37-43 ◽  
Author(s):  
C. Y. ZHANG ◽  
L. J. ZHANG ◽  
J. W. LI ◽  
J. H. LI ◽  
Z. M. WU ◽  
...  

2015 ◽  
Vol 141 (9) ◽  
pp. 1553-1561 ◽  
Author(s):  
Jing-Jing Chen ◽  
Ge Hong ◽  
Li-Jing Gao ◽  
Tian-Jun Liu ◽  
Wen-Jun Cao

Tumor Biology ◽  
2015 ◽  
Vol 37 (5) ◽  
pp. 6923-6933 ◽  
Author(s):  
Li-Jun Zhang ◽  
Yi-Jia Yan ◽  
Ping-Yong Liao ◽  
Davor Margetic ◽  
Li Wang ◽  
...  

2015 ◽  
Vol 08 (01) ◽  
pp. 1540003 ◽  
Author(s):  
Li-Jun Zhang ◽  
Lai-Xing Wang ◽  
Wei-Li Zhang ◽  
Yi-Jia Yan ◽  
Zhi-Long Chen

In this study, a novel photosensitizer meso-tetra (3-pyrrolidinomethyl-4-methoxyphenyl) chlorin (TPMC) was reported. It displays a characteristic long wavelength absorption peak at 656 nm and it shows a singlet oxygen quantum yield of 0.48. After light irradiation with 650 nm laser, it can kill Eca-109 and SMMC-7721 cells in vitro (25 mW/cm2, 1.2 to 3.6 J/cm2) and destroy Eca-109 tumor in nude mice (50 mW/cm2, 90 J/cm2). It has the perspective to be developed as a new anti-tumor drug in photodynamic therapy (PDT) photodiagnosis, and deserves further investigation.


2014 ◽  
Vol 11 (2) ◽  
pp. 204-212 ◽  
Author(s):  
Hongyou Zhao ◽  
Rong Yin ◽  
Defu Chen ◽  
Jie Ren ◽  
Yucheng Wang ◽  
...  

2019 ◽  
Vol 65 (5) ◽  
pp. 760-765
Author(s):  
Margarita Tyndyk ◽  
Irina Popovich ◽  
A. Malek ◽  
R. Samsonov ◽  
N. Germanov ◽  
...  

The paper presents the results of the research on the antitumor activity of a new drug - atomic clusters of silver (ACS), the colloidal solution of nanostructured silver bisilicate Ag6Si2O7 with particles size of 1-2 nm in deionized water. In vitro studies to evaluate the effect of various ACS concentrations in human tumor cells cultures (breast cancer, colon carcinoma and prostate cancer) were conducted. The highest antitumor activity of ACS was observed in dilutions from 2.7 mg/l to 5.1 mg/l, resulting in the death of tumor cells in all studied cell cultures. In vivo experiments on transplanted Ehrlich carcinoma model in mice consuming 0.75 mg/kg ACS with drinking water revealed significant inhibition of tumor growth since the 14th day of experiment (maximally by 52% on the 28th day, p < 0.05) in comparison with control. Subcutaneous injections of 2.5 mg/kg ACS inhibited Ehrlich's tumor growth on the 7th and 10th days of the experiment (p < 0.05) as compared to control.


2020 ◽  
pp. 1-12
Author(s):  
Maroeska J. Burggraaf ◽  
Lisette Waanders ◽  
Mariska Verlaan ◽  
Janneke Maaskant ◽  
Diane Houben ◽  
...  

BACKGROUND: Bladder cancer is the ninth most common cancer in men. 70% of these tumors are classified as non-muscle invasive bladder cancer and those patients receive 6 intravesical instillations with Mycobacterium bovis BCG after transurethral resection. However, 30% of patients show recurrences after treatment and experience severe side effects that often lead to therapy discontinuation. Recently, another vaccine strain, Salmonella enterica typhi Ty21a, demonstrated promising antitumor activity in vivo. Here we focus on increasing bacterial retention in the bladder in order to reduce the number of instillations required and improve antitumor activity. OBJECTIVE: To increase the binding of Ty21a to the bladder wall by surface labeling of the bacteria with adhesion protein FimH and to study its effect in a bladder cancer mouse model. METHODS: Binding of Ty21a with surface-labeled FimH to the bladder wall was analyzed in vitro and in vivo. The antitumor effect of a single instillation of Ty21a+FimH in treatment was determined in a survival experiment. RESULTS: FimH-labeled Ty21a showed significant (p <  0.0001) improved binding to mouse and human cell lines in vitro. Furthermore, FimH labeled bacteria showed ∼5x more binding to the bladder than controls in vivo. Enhanced binding to the bladder via FimH labeling induced a modest improvement in median but not in overall mice survival. CONCLUSIONS: FimH labeling of Ty21a significantly improved binding to bladder tumor cells in vitro and the bladder wall in vivo. The improved binding leads to a modest increase in median survival in a single bladder cancer mouse study.


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