Cancer Research Translational Cancer Medicine 2008: Cancer Clinical Trials and Personalized Medicine  Joint Metastasis Research Society-AACR Conference on Metastasis
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation

[Cancer Research 48, 5953-5955, November 1, 1988]
© 1988 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sinha, A. K.
Right arrow Articles by Watanabe, P. G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sinha, A. K.
Right arrow Articles by Watanabe, P. G.

Assessment of Cell Cycle Duration on the Incidence of Sister Chromatid Exchanges in Somatic and Spermatogonial Cells of the Rat

Anil K. Sinha1, V. Ann Linscombe, B. Bhaskar Gollapudi, John A. Zempel and Philip G. Watanabe

Health and Environmental Sciences-Texas, Lake Jackson Research Center, The Dow Chemical Company, Freeport, Texas 77541 [A. K. S., V. A. L., B. B. G., J. A. Z.]; and the Mammalian and Environmental Toxicology Research Laboratory, The Dow Chemical Company, Midland, Michigan 48640 [P. G. W.]

In order to examine the influence of the length of cell cycle on the incidence of sister chromatid exchanges (SCEs), average generation times and SCEs were studied in the presence of bromodeoxyuridine from spontaneously dividing rat lymph node, bone marrow, spleen, and spermatogonial cells. Average generation time differences among the three somatic cell types (lymph node, 7.6 h; bone marrow, 12.0 h; spleen, 14.9 h) were statistically significant as were the differences between the germinal cell (37.4 h) and each of the somatic cells. The SCE per cell frequencies were significantly higher in the somatic cells (lymph node, 6.8; bone marrow, 5.8; spleen, 6.1) as compared to the spermatogonial cells (1.6). However, no difference in SCE incidence was detected among the cells from the different somatic tissues. It was concluded that there was no simple relationship between cell cycle duration time and SCE formation.

1 To whom requests for reprints should be addressed, at Health and Environmental Sciences-Texas, The Dow Chemical Company, Lake Jackson Research Center 101, Freeport, TX 77541.

Received 2/ 8/88. Revised 4/29/88. Accepted 8/ 4/88.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Cell Growth & Differentiation
Copyright © 1988 by the American Association for Cancer Research.