The Radio-Sensitizing Effect of Pharmacological Concentration of Ascorbic Acid on Human Pancreatic Cancer Cells

被引:7
作者
Dayer, Dian [1 ]
Tabandeh, Mohammad R. [2 ,3 ]
Kazemi, Majid [4 ]
机构
[1] Ahvaz Jundishapur Univ Med Sci, Cellular & Mol Res Ctr, Ahvaz 61357831351, Iran
[2] Shahid Chamran Univ Ahvaz, Fac Vet Med, Dept Basic Sci, Div Biochem & Mol Biol, Ahvaz, Iran
[3] Shahid Chamran Univ Ahvaz, Stem Cells & Transgen Technol Res Ctr, Ahvaz, Iran
[4] Ahvaz Jundishapur Univ Med Sci, Med Fac, Dept Med Lab Sci, Ahvaz, Iran
关键词
Ascorbic acid; radiotherapy; pancreatic cancer; reactive oxygen species; Sax expression; Bcl2; expression; DNA fragmentation; HYDROGEN-PEROXIDE; VITAMIN-C; APOPTOSIS;
D O I
10.2174/1871520620666200612144124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Previous studies reported the inevitable destructive effects of radiotherapy on normal adjacent cells. Ascorbic Acid (AA) has been proposed as an effective anti-cancer agent with no obvious effects on normal cells. Objective: The effects of Ascorbic acid in combination with radiotherapy on human pancreatic carcinoma cell line were studied. Methods: The human pancreatic cancer cells were cultured and divided into four groups: control group (A) without any treatment, group B that received 2Gy radiotherapy alone, group C that was treated with 4mM AA alone, and group D that was co-treated with AA and radiotherapy. Cell viability, DNA fragmentation, expression of apoptotic genes, and Reactive Oxygen Species (ROS) production were determined in treated cells. Results: There was a noticeable decrease in cell viability after treatment with AA (and/or) radiotherapy. All treated groups showed elevated ROS production, Bax/Bcl2 expression, DNA fragmentation, and cytotoxycity compared with the control group. Cells under combination therapy showed the most cytotoxicity. Conclusion: The results suggest that AA at a dose of 4mmol/l may be used as an effective radio-sensitizing agent in pancreatic cancer cell line.
引用
收藏
页码:1927 / 1932
页数:6
相关论文
共 30 条
[1]  
[Anonymous], 1995, J ORTHOMOL MED
[2]  
[Anonymous], 2003, PHYS RAD THERAPY
[3]   Bax/Bcl-2 expression ratio in prediction of response to breast cancer radiotherapy [J].
Azimian, Hosein ;
Dayyani, Mahdieh ;
Toossi, Mohammad Taghi Bahreyni ;
Mahmoudi, Mahmoud .
IRANIAN JOURNAL OF BASIC MEDICAL SCIENCES, 2018, 21 (03) :325-332
[4]   Intravenous Vitamin C for Cancer Therapy - Identifying the Current Gaps in Our Knowledge [J].
Carr, Anitra C. ;
Cook, John .
FRONTIERS IN PHYSIOLOGY, 2018, 9
[5]   Pharmacologic ascorbic acid concentrations selectively kill cancer cells: Action as a pro-drug to deliver hydrogen peroxide to tissues [J].
Chen, Q ;
Espey, MG ;
Krishna, MC ;
Mitchell, JB ;
Corpe, CP ;
Buettner, GR ;
Shacter, E ;
Levine, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (38) :13604-13609
[6]   Ascorbate in pharmacologic concentrations selectively generates ascorbate radical and hydrogen peroxide in extracellular fluid in vivo [J].
Chen, Qi ;
Espey, Michael Graham ;
Sun, Andrew Y. ;
Lee, Je-Hyuk ;
Krishna, Murali C. ;
Shacter, Emily ;
Choyke, Peter L. ;
Pooput, Chaya ;
Kirk, Kenneth L. ;
Buettner, Garry R. ;
Levine, Mark .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (21) :8749-8754
[7]   Fluorine-18-Labeled Thymidine Positron Emission Tomography (FLT-PET) as an Index of Cell Proliferation after Pharmacological Ascorbate-Based Therapy [J].
Cieslak, John A. ;
Sibenaller, Zita A. ;
Walsh, Susan A. ;
Ponto, Laura L. Boles ;
Du, Juan ;
Sunderland, John J. ;
Cullen, Joseph J. .
RADIATION RESEARCH, 2016, 185 (01) :31-38
[8]   Sonic hedgehog pathway suppression and reactivation accelerates differentiation of rat adipose-derived mesenchymal stromal cells toward insulin-producing cells [J].
Dayer, Dian ;
Tabar, Mahmoud Hashemi ;
Moghimipour, Eskandar ;
Tabandeh, Mohammad Reza ;
Ghadiri, Ata A. ;
Bakhshi, Elham Allah ;
Orazizadeh, Mahmoud ;
Ghafari, Mohammad Ali .
CYTOTHERAPY, 2017, 19 (08) :937-946
[9]   Mechanisms of Ascorbate-Induced Cytotoxicity in Pancreatic Cancer [J].
Du, Juan ;
Martin, Sean M. ;
Levine, Mark ;
Wagner, Brett A. ;
Buettner, Garry R. ;
Wang, Sih-han ;
Taghiyev, Agshin F. ;
Du, Changbin ;
Knudson, Charles M. ;
Cullen, Joseph J. .
CLINICAL CANCER RESEARCH, 2010, 16 (02) :509-520
[10]  
Farhood B, 2018, IRAN J PUBLIC HEALTH, V47, P309