Treadmill exercise-dependent tumor growth retardation in T-cell lymphoma-bearing host displays gender dimorphism

Oncol Res. 2010;18(7):293-304. doi: 10.3727/096504010x12629634366142.

Abstract

A number of previous investigations have reported that physical exercise renders immunopotentiating and antitumor therapeutic benefits to the tumor-bearing host. As these effects of physical exercise are mainly mediated through the modulation of hormonal and cytokine repertoire, it remains unclear if male and female tumor-bearing hosts show a gender-dependent differential response to the therapeutic action of physical exercise in tumor growth retardation. In the present investigation tumor growth retardation, following physical exercise was investigated in a gender-specific manner in a murine tumor model of a T-cell lymphoma designated as Dalton's lymphoma (DL). The results of the present investigation show that physical exercise of a tumor-bearing host on a treadmill results in a better retardation of tumor progression along with prolongation of survival time in male compared to female tumor-bearing host. Such gender dimorphism of the therapeutic benefits of physical exercise in tumor-bearing host was found to be associated with a gender-dependent variation in cell survival and induction of apoptosis in tumor cells. Moreover, expression of cell growth regulatory proteins-selectin, Hsp70, p53, CAD, SOCS, and IL-2 receptor-was found to vary in a gender-specific manner following physical exercise. The investigation also indicates the role of cytokines and macrophages in manifestation of gender dimorphism in the response of tumor-bearing mice to physical exercise. Thus, the observations of the present investigation suggest for the first time that the beneficial effects of physical exercise in a tumor-bearing host may be variable depending on the gender of the host.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Aspartate Carbamoyltransferase / metabolism
  • Blotting, Western
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing) / metabolism
  • Cell Proliferation
  • Dihydroorotase / metabolism
  • Disease Models, Animal
  • Exercise Therapy / methods*
  • Female
  • HSP70 Heat-Shock Proteins / metabolism
  • Lymphoma, T-Cell / metabolism
  • Lymphoma, T-Cell / pathology
  • Lymphoma, T-Cell / therapy*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Physical Conditioning, Animal*
  • Receptors, Interleukin-2 / metabolism
  • Selectins / metabolism
  • Sex Factors
  • Suppressor of Cytokine Signaling Proteins / metabolism
  • Survival Rate
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • CAD trifunctional enzyme
  • HSP70 Heat-Shock Proteins
  • Receptors, Interleukin-2
  • Selectins
  • Suppressor of Cytokine Signaling Proteins
  • Tumor Suppressor Protein p53
  • Aspartate Carbamoyltransferase
  • Dihydroorotase
  • Carbamoyl-Phosphate Synthase (Glutamine-Hydrolyzing)