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Cell turnover in the “resting” human breast: influence of parity, contraceptive pill, age and laterality

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Anderson, T J, Ferguson, D J, Raab, G M·1982·British Journal of Cancer

Abstract

Morphological identification of cell multiplication (mitosis) and cell deletion (apoptosis) within the lobules of the "resting" human breast is used to assess the response of the breast parenchyma to the menstrual cycle. The responses are shown to have a biorhythm in phase with the menstrual cycle, with a 3-day separation of the mitotic and apoptotic peaks. The study fails to demonstrate significant differences in the responses between groups defined according to parity, contraceptive-pill use or presence of fibroadenoma. However, significant differences are found in the apoptotic response according to age and laterality. The results highlight the complexity of modulating influences on breast parenchymal turnover in the "resting" state, and prompt the investigation of other factors as well as steroid hormones and prolactin in the promotion of mitosis. The factors promoting apoptosis in the breast are still not clear.

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Metadata

Authors
Anderson, T. J., Ferguson, D. J., & Raab, G. M.
Venue
British Journal of Cancer
Published
1982-09
Volume
46
Issue
3
Pages
376-382
ISSN
  • 0007-0920 (ISSN-L)
  • 1532-1827
OpenAlex
W2025896944
Cited by
241
References
0
FWCI
2.79
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Cell turnover in the “resting” human breast: influence of parity, contraceptive pill, age and laterality. https://app.cochat.ai/papers/10.1038/bjc.1982.213
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Anderson, T. J., Ferguson, D. J., & Raab, G. M. (1982). Cell turnover in the “resting” human breast: influence of parity, contraceptive pill, age and laterality. British Journal of Cancer. https://doi.org/10.1038/bjc.1982.213

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.