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Expression of apoptosis regulatory proteins in the skeletal muscle of tumor-bearing rabbits compared with diet-restricted rabbits.

Abstract
The mechanism of body weight loss in the tumor-bearing state is still unclear. In this study, we investigated expressions of apoptosis regulatory proteins in the skeletal muscle of tumor-bearing and diet-restricted rabbits, and tried to evaluate the differences between the two groups. The apoptotic index (AI) in the tumor-bearing group was 28.1+/-2.84 on day 10. By day 20, many more apoptotic cells were found (AI: 40.5+/-3.20), but then after day 20 their numbers gradually decreased (AI: 9.67+/-2.22 on day 30 and 0.93+/-0.96 on day 40). By contrast, no apoptotic cells were detected in the diet-restricted group at any of the times examined. Bcl-2 immunoreactivity was either not detected at all or only weakly observed in both groups. By contrast, Bax expression increased gradually after implantation in the tumor-bearing group. Bax expression in skeletal muscle cell was graded (moderate) 10 days after tumor implantation, and (high) by day 20, in 2 of the 5 tumor-bearing rabbits. After day 20, however, Bax immunoreactivity decreased continuously in the tumor-bearing group. By contrast, hardly any Bax-immuno-positive cells were detected in the diet-restricted group. These results suggest that loss of body weight in the tumor-bearing group is different from that in the diet-restricted group, and is related to apoptosis of skeletal muscles.
AuthorsO Ishiko, T Sumi, H Yoshida, Y Hyun, S Ogita
JournalInternational journal of molecular medicine (Int J Mol Med) Vol. 8 Issue 3 Pg. 279-83 (Sep 2001) ISSN: 1107-3756 [Print] Greece
PMID11494056 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-bcl-2
  • bcl-2-Associated X Protein
Topics
  • Adipose Tissue
  • Animals
  • Apoptosis (genetics)
  • Body Mass Index
  • Body Weight
  • DNA Fragmentation (genetics)
  • Diet, Reducing
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Male
  • Muscle, Skeletal (chemistry, metabolism, pathology)
  • Neoplasm Transplantation
  • Neoplasms, Experimental (genetics, metabolism, physiopathology)
  • Proto-Oncogene Proteins (biosynthesis)
  • Proto-Oncogene Proteins c-bcl-2 (biosynthesis)
  • Rabbits
  • Time Factors
  • bcl-2-Associated X Protein

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