Chromosomal radiosensitivity in G 2-phase lymphocytes identifies breast cancer patients with distinctive tumour characteristics

70Citations
Citations of this article
14Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

A substantial proportion of women with breast cancer exhibit an abnormally high radiosensitivity as measured by the frequency of chromatid breaks induced in G 2-phase, PHA stimulated lymphocytes. Chromatid break frequencies were compared for a cohort of previously untreated sporadic breast cancer patients and hospital outpatient controls. In the breast cancer group 46% showed high radiosensitivity compared to 14% of controls (P < 0.001). Comparison of those breast cancer patients with a high G 2 radiosensitivity (G 2RS) versus those with a low G 2RS showed no difference in menopausal status or age but the high G 2RS group had on average a lower score on the Nottingham Prognostic Index. Predicted survival in the high G 2RS group at 15 years was 55% compared to 36% for the low G 2RS group. Furthermore, 81% of tumours from the high G 2RS were oestrogen receptor positive compared to 45% from the low G 2RS group. Thus high G 2RS identifies a sub-population of patients with distinctive tumour characteristics and with a predicted improved prognosis as compared with those in the low G 2RS group. Our findings imply that besides influencing risk of breast cancer the genetic factors determining G 2 radiosensitivity also influence the tumour characteristics and prognosis in these patients. © 2001 Cancer Research Campaign.

Cite

CITATION STYLE

APA

Riches, A. C., Bryant, P. E., Steel, C. M., Gleig, A., Robertson, A. J., Preece, P. E., & Thompson, A. M. (2001). Chromosomal radiosensitivity in G 2-phase lymphocytes identifies breast cancer patients with distinctive tumour characteristics. British Journal of Cancer, 85(8), 1157–1161. https://doi.org/10.1054/bjoc.2001.2086

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free