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Cited by 303

The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.

Cholesterol and prostate cancer

Open access
Pelton, Kristine, Freeman, Michael R, Solomon, Keith R·2012·Current Opinion in Pharmacology

Abstract

Summary Prostate cancer risk can be modified by environmental factors, however the molecular mechanisms affecting susceptibility to this disease are not well understood. As a result of a series of recently published studies, the steroidal lipid, cholesterol, has emerged as a clinically relevant therapeutic target in prostate cancer. This review summarizes the findings from human studies as well as animal and cell biology models which suggest that high circulating cholesterol increases risk of aggressive prostate cancer, while cholesterol lowering strategies may confer protective benefit. Relevant molecular processes that have been experimentally tested and might explain these associations are described. We suggest that these promising results now could be applied prospectively to attempt to lower risk of prostate cancer in select populations.

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Crossref · 10.1016/j.coph.2012.07.006

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Metadata

Authors
Pelton, K., Freeman, M. R., & Solomon, K. R.
Venue
Current Opinion in Pharmacology
Publisher
Elsevier BV
Published
2012-12
Volume
12
Issue
6
Pages
751-759
ISSN
1471-4892 (ISSN-L)
OpenAlex
W2014393189
Cited by
303
References
1
FWCI
1.18
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cholesterol and prostate cancer. https://app.cochat.ai/papers/10.1016/j.coph.2012.07.006
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Pelton, K., Freeman, M. R., & Solomon, K. R. (2012). Cholesterol and prostate cancer. Current Opinion in Pharmacology. https://doi.org/10.1016/j.coph.2012.07.006

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

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.