Role of beta-carotene on the changes in activity patterns and levels of biotransforming enzymes in transplantable murine lymphoma

Cancer Lett. 1995 Apr 14;90(2):191-7. doi: 10.1016/0304-3835(95)03711-5.

Abstract

The differential levels of induction of hepatic microsomal cytochrome P-450 (cyt. P-450), UDP-glucuronyl transferase (UDPGT) and cytosolic glutathione-S-transferase (GST) activities were evaluated over various periods of time, following tumor transplantation in male Swiss albino mice in the presence and absence of beta-carotene supplementation in their basal diet (100 mg/kg). An increase in the total hepatic microsomal cytochrome P-450 and UDP-glucuronyl transferase and cytosolic GSH-transferase activities (1.5 to 2 fold) occurred during the later stage of tumor progression (22 +/- 2 days onwards). However, beta-carotene supplementation throughout the study increased or decreased the random activity trends of the above markers significantly (P < 0.05- < 0.01). Finally, beta-carotene supplementation could enhance the survival of the host bearing lymphoma by almost 2-fold (50-60 days) over and above the lymphoma controls (30-35 days).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Biotransformation / drug effects*
  • Carotenoids / pharmacology*
  • Carotenoids / therapeutic use
  • Cytochrome P-450 Enzyme System / metabolism
  • Glucuronosyltransferase / metabolism
  • Glutathione Transferase / metabolism
  • Lymphoma, T-Cell / drug therapy*
  • Lymphoma, T-Cell / enzymology*
  • Male
  • Mice
  • Microsomes, Liver / enzymology
  • Mixed Function Oxygenases / metabolism
  • Neoplasm Transplantation
  • Peritoneal Neoplasms / drug therapy
  • Peritoneal Neoplasms / enzymology
  • beta Carotene

Substances

  • Anticarcinogenic Agents
  • Antineoplastic Agents
  • beta Carotene
  • Carotenoids
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Glucuronosyltransferase
  • Glutathione Transferase