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dc.contributor.authorChebet, J.J.
dc.contributor.authorEhiri, J.E.
dc.contributor.authorMcClelland, D.J.
dc.contributor.authorTaren, D.
dc.contributor.authorHakim, I.A.
dc.date.accessioned2021-09-09T21:28:01Z
dc.date.available2021-09-09T21:28:01Z
dc.date.issued2021
dc.identifier.citationChebet, J. J., Ehiri, J. E., McClelland, D. J., Taren, D., & Hakim, I. A. (2021). Effect of d-limonene and its derivatives on breast cancer in human trials: A scoping review and narrative synthesis. BMC Cancer, 21(1).
dc.identifier.issn1471-2407
dc.identifier.doi10.1186/s12885-021-08639-1
dc.identifier.urihttp://hdl.handle.net/10150/661474
dc.description.abstractBackground: D-limonene and its derivatives have demonstrated potential chemopreventive and anticancer activity in preclinical and clinical studies. The aim of this scoping review was to assess and critically appraise current literature on the effect of these bioactive citrus peel compounds on breast cancer in human trials and to identify knowledge gaps for exploration in future studies. Methods: This study followed a scoping review framework. Peer-reviewed journal articles were included if they reported the effect of d-limonene or its derivatives on breast cancer in human subjects. Articles were retrieved from academic databases – PubMed, EMBASE, CINAHL, Web of Science, and Cochrane reviews – and iteratively through review of bibliographies of relevant manuscripts. Titles and abstracts were appraised against the aforementioned inclusion criteria in a first round of screening. Through consensus meetings and full article review by authors, a final set of studies were selected. Results were reported according to the PRISMA extension for scoping reviews. Results: Our search strategy yielded 367 records. Following screening and adjudication, five articles reporting on phase 1(n = 2), phase 2 (n = 2) and both trial phases (n = 1) were included as the final dataset for this review. Trials evaluating the effect of d-limonene (n = 2) showed it was well tolerated in subjects. One study (n = 43 participants) showed d-limonene concentrated in breast tissue (mean 41.3 μg/g tissue) and reduction in tumor cyclin D1 expression, which is associated with tumor proliferation arrest. This study did not show meaningful change in serum biomarkers associated with breast cancer, except for a statistically significant increase in insulin-like growth factor-1 (IGF-I) levels. While elevation of IGF-I is associated with increased cancer risk, the clinical implication of this study remains uncertain given its short duration. Trials with perillyl alcohol (n = 3) showed low tolerance and no effect on breast cancer. Conclusion: This review demonstrated a dearth of clinical studies exploring the effect of d-limonene and its derivatives on breast cancer. Limited literature suggests d-limonene is safe and tolerable in human subjects compared to its derivative, perillyl alcohol. Our review demonstrates the need for additional well-powered placebo-controlled trials that assess d-limonene’s efficacy on breast cancer compared to other therapies. © 2021, The Author(s).
dc.language.isoen
dc.publisherBioMed Central Ltd
dc.rightsCopyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectBreast cancer
dc.subjectChemopreventive
dc.subjectCitrus peel
dc.subjectD-limonene
dc.subjectPerillyl alcohol
dc.subjectScoping review
dc.titleEffect of d-limonene and its derivatives on breast cancer in human trials: a scoping review and narrative synthesis
dc.typeArticle
dc.typetext
dc.contributor.departmentDepartment of Health Promotion Sciences, Mel and Enid Zuckerman College of Public Health, University of Arizona
dc.contributor.departmentDepartment of Health Promotion Sciences, Mel and Enid Zuckerman College of Public Health, University of Arizona
dc.contributor.departmentUniversity of Arizona Health Sciences Library, University of Arizona
dc.identifier.journalBMC Cancer
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitleBMC Cancer
refterms.dateFOA2021-09-09T21:28:01Z


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Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.
Except where otherwise noted, this item's license is described as Copyright © The Author(s) 2021. This article is licensed under a Creative Commons Attribution 4.0 International License.