Inhibition of cell growth induced by photosensitizer PP(Arg)2-mediated photodynamic therapy in human breast and prostate cell lines. Part I

被引:8
|
作者
Nowak-Stepniowska, Agata [1 ,2 ]
Malecki, Maciej [3 ]
Wiktorska, Katarzyna [4 ]
Romiszewska, Anna [1 ]
Padzik-Graczyk, Alfreda [1 ]
机构
[1] Mil Univ Technol, Biochem & Spect Lab, Inst Optoelect, PL-00908 Warsaw, Poland
[2] Mil Univ Technol, Inst Chem, PL-00908 Warsaw, Poland
[3] M Sklodowska Curie Canc Ctr, Dept Cell Biol, PL-02781 Warsaw, Poland
[4] Natl Med Inst, Dept Cell Biol, Confocal Microscopy Lab, PL-00725 Warsaw, Poland
关键词
Photodynamic therapy; Clonogenic assay; Breast cancer cell lines; Prostate cancer cell lines; Cancer growth stimulation; DIAMINO ACID-DERIVATIVES; CANCER; PORPHYRINS; MECHANISMS; INDUCTION; TUMORS; MODES; MICE;
D O I
10.1016/j.pdpdt.2010.09.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Photodynamic therapy can become an effective alternative method to surgery. The experiments reveal that using low photosensitizer doses and relatively low energy doses allow us to obtain effective results after PDT (to limit formation of colonies by investigated cancer cells). The prostate and breast cancer cell lines were investigated: MCF-7, a human breast cancer responsive to androgen therapy; MDA-MB231, a more aggressive human breast cancer non-responsive to androgen therapy; LNCaP, a lymphonodal metastasis of prostate carcinoma responsive to androgen therapy; DU-145, a human prostate cancer non-responsive to androgen therapy. Clonogenic assay shows that certain PP(Arg)(2) and light energy low doses stimulate the researched colony-forming cancer cells growth. Some low energy doses used during PP(Arg)(2)-mediated PDT also cause the increase in the colony-forming tumor cells. Among investigated cancer lines, MCF-7 exhibited the biggest sensibility towards PP(Arg)(2) and LNCaP the smallest one. PP(Arg)(2) based PDT is an effective method in colony growth limitation of breast cancer cell lines: MCF-7, MDA-MB231 and prostate cancer cell lines: LNCaP, DU-145. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 48
页数:10
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