Modulation of tricarboxylic acid cycle dehydrogenases during hepatocarcinogenesis induced by hexachlorocyclohexane in mice

被引:9
作者
Bhatt, Devendra Kumar [1 ]
Bano, Mehajbeen [1 ]
机构
[1] Mohan Lal Sukhadia Univ, Dept Zool, Canc Biol & Toxicol Lab, Udaipur 313001, India
关键词
Hexachlorocyclohexane; TCA cycle dehydrogenases; Hepatocarcinoma; NADP(+)-DEPENDENT ISOCITRATE DEHYDROGENASE; OXIDATIVE STRESS; POLYCHLORINATED-BIPHENYLS; PESTICIDE-RESIDUES; RAT-LIVER; METABOLISM; CANCER; TUMORS; BIOENERGETICS; CYTOTOXICITY;
D O I
10.1016/j.etp.2008.09.004
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The sequential distribution of key tricarboxylic acid (TCA) cycle enzymes have been investigated during hexachlorocyclohexane (HCH)-induced hepatocarcinogenesis in Swiss mice. Animals were continuously exposed to HCH (500 ppm) for 2, 4, and 6 months until liver tumor developed. The activity of TCA cycle enzymes such as isocitrate dehydrogenase (ICDH), succinate dehydrogenase (SDH), and malate dehydrogenase (MDH) have been studied. The activity of all the enzymes declined after 2 months of exposure of HCH in the liver. The neoplastic nodules and tumors developed after an exposure of HCH for 4 and 6 months, respectively. Neoplastic nodule and tumor showed wide variations in the activity and distribution of TCA cycle enzymes. The decreasing pattern in the activity of enzymes persisted in the non-neoplastic and non-tumor regions of the liver except SDH. However, the cells in nodular area and tumor showed intense enzymatic activities at cellular level. In the nodular region SDH activity declined prominently, whereas the non-nodular area showed positive reaction. Conspicuously, the tumor showed islands of positive and negative zones for TCA cycle dehydrogenases. The significance and relevance of such a distribution pattern still remains a mystery. The results are discussed in the light of HCH-induced toxicity on energy metabolism in exposed animals and possible role of such enzymes in the tumor formation. (C) 2008 Elsevier GmbH. All rights reserved.
引用
收藏
页码:325 / 332
页数:8
相关论文
共 39 条
[1]  
[Anonymous], 2006, J CARCINOG, DOI DOI 10.1186/1477-3163-5-14
[2]   THE FORMATION OF CHLOROBENZENE AND BENZENE BY THE REDUCTIVE METABOLISM OF LINDANE IN RAT-LIVER MICROSOMES [J].
BAKER, MT ;
NELSON, RM ;
VANDYKE, RA .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 236 (02) :506-514
[3]   Contamination of liquid milk and butter with pesticide residues in the Ludhiana district of Punjab state, India [J].
Battu, RS ;
Singh, B ;
Kang, BK .
ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY, 2004, 59 (03) :324-331
[4]  
BHATT DK, 1981, CELL MOL BIOL, V27, P231
[5]   Tricarboxylic acid cycle dysfunction as a cause of human diseases and tumor formation [J].
Briere, Jean-Jacques ;
Favier, Judith ;
Gimenez-Roqueplo, Anne-Paule ;
Rustin, Pierre .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2006, 291 (06) :C1114-C1120
[6]   Hypoxia and oxidative stress in breast cancer - Oxidative stress: its effects on the growth, metastatic potential and response to therapy of breast cancer [J].
Brown, NS ;
Bicknell, R .
BREAST CANCER RESEARCH, 2001, 3 (05) :323-327
[7]   Mitochondrial defects in cancer [J].
Carew J.S. ;
Huang P. .
Molecular Cancer, 1 (1)
[8]   Oncogenic alterations of metabolism [J].
Dang, CV ;
Semenza, GL .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (02) :68-72
[9]   PRENATAL EXPOSURE TO POLYCHLORINATED-BIPHENYLS - EFFECTS ON BIRTH SIZE AND GESTATIONAL-AGE [J].
FEIN, GG ;
JACOBSON, JL ;
JACOBSON, SW ;
SCHWARTZ, PM ;
DOWLER, JK .
JOURNAL OF PEDIATRICS, 1984, 105 (02) :315-320
[10]   Increased metabolizing activities of the tricarboxylic acid cycle and decreased drug metabolism in hepatocellular carcinoma [J].
Fukuda, H ;
Ebara, M ;
Okuyama, M ;
Sugiura, N ;
Yoshikaw, M ;
Saisho, H ;
Shimizu, R ;
Motoji, N ;
Shigematsu, A ;
Watayo, T .
CARCINOGENESIS, 2002, 23 (12) :2019-2023