Apoptosis of human bladder cancer BIU-87 cells after photodynamic therapy with laser-activated BPD-MA determined with TUNEL assays
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1.
Institute of Ultrasound Imaging, Chongqing University of Medical Sciences, Chongqing 400010, China;
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2.
Xinqiao Hospital, Third Military Medical University, Chongqing 400037, China;
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3.
Department of Laser Research, Rehabilitation Center, Second Affiliated Hospital, Chongqing University of Medical Sciences, Chongqing 400010, China;
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4.
Center of Plastic Surgery, Southwest Hospital, Third Military Medical University, Chongqing 400038, China
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Received Date:
2004-12-16
Accepted Date:
2005-01-25
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Abstract
In order to study the mechanism of photodynamic therapy on malignant tumors,photosensitization of BPD-MA is activated by laser with red light(632.8nm) delivered at 10mW/cm2to give a total dose of 2.4J/cm2.Apoptosis of human bladder cancer BIU-87 cells is determined with flow cytometry with PI staining and terminal deoxyuridine nick end labeling(TUNEL) assays.Results show that photodynamic therapy with BPD-MA significantly increases the rate of apoptosis in BIU-87 cells.A lot of the positive cells in which their nucleus is brown-yellow fine particle shape or overflowing-dispersed are observed after treatment of cells with photodynamic therapy with BPD-MA.However,laser irradiation alone,BPD-MA alone and sham radiation without BPD-MA can not affect apoptosis of human bladder cancer BIU-87 cells.A conclusion can be made that treatment of cells with photodynamic therapy obviously induces human bladder cancer BIU-87 cells to apoptosis,which may be one of the important mechanism of photodynamic therapy on malignant tumors.
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References
[1]
|
CHEN Zh L,ZHANG L M,SUN J et al.The photodynamic and chemotherapeutic effect of porphyrin nitrogen mustard on liver cancer cell SMMC7721[J].Academic Journal of Second Military Medical University,2001,22(3):271~273(in Chinese). |
[2]
|
XU Ch S,YU Q,WU Sh M et al.Leukemia cell purging through photodynamic therapy with oligonucleotide modified by photosensitizer[J].Laser Technology,2002,26(2):159~160(in Chinese). |
[3]
|
WANG R P,LI Y X.Application of photodynamic therapy in management of tumors[J].Biomedicine and Engineering of Foreign Medical Sciences,1999,22(6):355~358(in Chinese). |
[4]
|
WANG T Y,MA J Sh.As the light took effect,the symptoms van-ished-introduction of photodynamic therapy[J].Nature Journal,2001,22(5):276~281(in Chinese). |
[5]
|
THOMPSON H J,STRANGE R,SCHEDIN P J et al.Apoptosis in the genesis and prevention of cancer[J].Cancer Epidemollogy Biomarkers Prevention,1992,1(1):597~603. |
[6]
|
GUO D Y,CHEN Y Sh,BIAN X W et al.Study of nordihydroguaiaretic acid-induced apoptosis in human malignant glioma cell line[J].Cancer,2001,20(11):1246(in Chinese). |
[7]
|
HETTS S W.To die or not to die:an overview of apoptosis and its role in disease[J].Journal of the American Medical Association,1998,279(4):300~307. |
[8]
|
FESUS L,SZONDY Z,URA Y I.Probing the molecular program of apoptosis by cancer chemotherapeutic agents[J].Journal of Cell Biochemistry,1995,22(suppl 1):151~161. |
[9]
|
ORMEROD M G.The study of apoptotic cells by flow cytometry[J].Leukemia,1998,12(7):1013~1025. |
[10]
|
PENG L M.Contrastive study of six assays for apoptosis[J].Chinese Journal of Pathology,1999,28(1):55~57(in Chinese). |
[11]
|
LIU A Q,LIU D Q,GU Y et al.Effects of copper vapor laser irradiation on apoptosis and proliferation inhibiting of vascular smooth muscle cells[J].Laser Journal,2002,23(6):71~72(in Chinese). |
[12]
|
GUPTA S,HUSSIAN T,MUKHTAR H.Molecular pathway for c-epigallocatech in-3-gallate-induced cell cycle arrest and apoptosis of human prostate carcinoma cells[J].Archives of Biochemistry and Biophysics,2003,4(1):177~185. |
[13]
|
GAVRIELI Y,SHERMAN Y,BEN-SASSON S A.Identification ofprogrammed cell death in situ via specific labeling of nuclear DNA fragment[J].Journal of Cell Biology,1992,119(3):493~501. |
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