Impact of Breast Cancer and Combination Chemotherapy on Oxidative Stress, Hepatic and Cardiac Markers

被引:28
作者
Amin, Kamal Adel [1 ]
Mohamed, Basant Mahmoud [2 ]
El-wakil, Mohamed Aly M. [3 ]
Ibrahem, Sanaa Omar [2 ]
机构
[1] Beni Suef Univ, Dept Biochem, Fac Vet Med, Bani Suwayf 62511, Egypt
[2] Beni Suef Univ, Dept Chem, Fac Sci, Bani Suwayf 62511, Egypt
[3] Beni Suef Univ, Dept Clin Oncol, Fac Med, Bani Suwayf 62511, Egypt
关键词
Breast neoplasms; Cardiac function; Chemotherapy; Liver function; Oxidative stress; ANTIOXIDANT STATUS; LIPID-PEROXIDATION; INDUCED CARDIOTOXICITY; NADH DEHYDROGENASE; HEART-MITOCHONDRIA; NITRIC-OXIDE; ALBINO RATS; DOXORUBICIN; BLOOD; TOXICITY;
D O I
10.4048/jbc.2012.15.3.306
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose: Carcinoma of the breast is the most prevalent cancer among Egyptian women and constitutes 29% of National Cancer Institute cases. The aim of this study was to determine the effect of breast cancer on oxidative stress, cardiac markers and liver function tests, moreover the role of 5-fluorouracil, doxorubicin, and cyclophosphamide (FAC) in the treatment of breast cancer and its mechanism through changing the measured markers. Methods: Forty female breast cancer patients who were admitted to the Department of Oncology of the Beni-Suef University Hospital were enrolled in the study. This study included three arms: a control group of healthy age-matched females (n=20), breast cancer patients who weren't receiving treatment (n=20), and patients undergoing treatment with anticancer combination drugs FAC (n=20). Blood samples collected from the control subjects and patients were analysed to determine levels of catalase, reduced glutathione (GSH), uric acid, nitric oxide (NO), malondialdehyde, creatine kinase (CK), lactate dehydrogenase (LDH), liver enzymes (alanine aminotransferase and aspartate aminotransferase), and creatinine. Results: The levels of catalase and GSH were significantly reduced (p<0.05) in breast carcinoma and FAC treated breast cancer patients. The lipid peroxidation and NO levels were significantly enhanced in both untreated and FAC treated breast cancer patients. The CK and LDH were significantly enhanced (p<0.05) in the FAC group. Conclusion: The results from the present study show that oxidative stress is implicated in breast carcinoma and chemotherapy aggravates this oxidative stress which causes damage to many cellular targets and has the main side effect of cardiotoxicity.
引用
收藏
页码:306 / 312
页数:7
相关论文
共 30 条
[1]
Redox regulation in cancer A double-edged sword with therapeutic potential [J].
Acharya, Asha ;
Das, Ila ;
Chandhok, Des ;
Saha, Tapas .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2010, 3 (01) :23-34
[2]
Doxorubicin toxicity can be ameliorated during antioxidant L-carnitine supplementation [J].
Alshabanah, Othman A. ;
Hafez, Mohamed M. ;
Al-Harbi, Mohamed M. ;
Hassan, Zeinab K. ;
Al Rejaie, Salim S. ;
Asiri, Yosef A. ;
Sayed-Ahmed, Mohamed M. .
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY, 2010, 3 (06) :428-433
[3]
Candidate pathways linking inducible nitric oxide synthase to a basal-like transcription pattern and tumor progression in human breast cancer [J].
Ambs, Stefan ;
Glynn, Sharon A. .
CELL CYCLE, 2011, 10 (04) :619-624
[4]
BEUTLER E, 1963, J LAB CLIN MED, V61, P882
[5]
[6]
BURTIS CA, 1998, TIETZ TXB CLIN CHEM, P1034
[7]
MEASUREMENT OF CATALASE ACTIVITY IN TISSUE EXTRACTS [J].
COHEN, G ;
DEMBIEC, D ;
MARCUS, J .
ANALYTICAL BIOCHEMISTRY, 1970, 34 (01) :30-+
[8]
Conklin Kenneth A, 2004, Integr Cancer Ther, V3, P294, DOI 10.1177/1534735404270335
[9]
Dystrophin-deficiency increases the susceptibility to doxorubicin-induced cardiotoxicity [J].
Deng, Shiwei ;
Kulle, Bettina ;
Hosseini, Mehdi ;
Schlueter, Gregor ;
Hasenfuss, Gerd ;
Wojnowski, Leszek ;
Schmidt, Albrecht .
EUROPEAN JOURNAL OF HEART FAILURE, 2007, 9 (10) :986-994
[10]
FOSSATI P, 1980, CLIN CHEM, V26, P227