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Cytoplasmic Cyclin E Predicts Recurrence in Patients with Breast Cancer

Hunt, Kelly K.; Karakas, Cansu; Ha, Min Jin; Biernacka, Anna; Yi, Min; Sahin, Aysegul; Adjapong, Opoku; Hortobogyi, Gabriel N.; Bondy, Melissa L.; Thompson, Patricia A.; Cheung, Kwok Leung; Ellis, Ian O.; Bacus, Sarah; Symmans, W. Fraser; Do, Kim-Anh; Keyomarsi, Khandan

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Authors

Kelly K. Hunt

Cansu Karakas

Min Jin Ha

Anna Biernacka

Min Yi

Aysegul Sahin

Opoku Adjapong

Gabriel N. Hortobogyi

Melissa L. Bondy

Patricia A. Thompson

Ian O. Ellis

Sarah Bacus

W. Fraser Symmans

Kim-Anh Do

Khandan Keyomarsi



Abstract

Background: Low-molecular-weight-cyclin E (LMW-E) detected by Western blot, predicts for reduced breast cancer survival, however, it is impractical for clinical use. LMW-E lacks a nuclear localization signal which leads to accumulation in the cytoplasm that can be detected by immunohistochemistry. We tested the hypothesis that cytoplasmic staining of cyclin E can be used as a predictor of poor outcome in different subtypes of breast cancer using patient cohorts with distinct clinical and pathologic features. Methods: We evaluated the subcellular localization of cyclin E in breast cancer specimens from 2,494 patients from 4 different cohorts: 303 from a prospective study and 2,191 from retrospective cohorts (National Cancer Institute [NCI], MD Anderson Cancer Center [MDA] and the United Kingdom [UK]). Median follow-up times were 8.0, 10.1, 13.5, and 5.7 years, respectively. Results: Subcellular localization of cyclin E on immunohistochemistry was associated with full-length (nuclear) and low molecular weight isoforms (cytoplasmic) of cyclin E on Western blot analysis. In multivariable analysis, cytoplasmic cyclin E staining was associated with the greatest risk of recurrence compared with other prognostic factors across all subtypes in three (NCI, MDA and UK) of the cohorts. In the MDA cohort, cytoplasmic cyclin E staining outperformed Ki67 and all other variables as prognostic factors. Conclusion: Cytoplasmic cyclin E, identifies patients with the highest likelihood of recurrence consistently across different patient cohorts and subtypes. These patients may benefit from alternative therapies targeting the oncogenic isoforms of cyclin E.

Citation

Hunt, K. K., Karakas, C., Ha, M. J., Biernacka, A., Yi, M., Sahin, A., …Keyomarsi, K. (2017). Cytoplasmic Cyclin E Predicts Recurrence in Patients with Breast Cancer. Clinical Cancer Research, 23(12), 2991-3002. https://doi.org/10.1158/1078-0432.ccr-16-2217

Journal Article Type Article
Acceptance Date Nov 8, 2016
Online Publication Date Nov 23, 2016
Publication Date Jun 15, 2017
Deposit Date Dec 7, 2016
Publicly Available Date Dec 7, 2016
Journal Clinical Cancer Research
Print ISSN 1078-0432
Electronic ISSN 1557-3265
Publisher American Association for Cancer Research
Peer Reviewed Peer Reviewed
Volume 23
Issue 12
Pages 2991-3002
DOI https://doi.org/10.1158/1078-0432.ccr-16-2217
Keywords Cytoplasmic cyclin E, breast cancer, biomarker, cell cycle
Public URL https://nottingham-repository.worktribe.com/output/827251
Publisher URL https://clincancerres.aacrjournals.org/content/23/12/2991
Contract Date Dec 7, 2016