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Review
. 2016 Jan 5;7(3):232-40.
doi: 10.7150/jca.13403. eCollection 2016.

Vitamin D and Colorectal, Breast, and Prostate Cancers: A Review of the Epidemiological Evidence

Affiliations
Review

Vitamin D and Colorectal, Breast, and Prostate Cancers: A Review of the Epidemiological Evidence

Elizabeth T Jacobs et al. J Cancer. .

Abstract

Over the past two decades, the question of whether vitamin D has a role in cancer incidence, progression, and mortality has been studied in detail. Colorectal, breast, and prostate cancers have been a particular area of focus; together, these three malignancies account for approximately 35% of cancer cases and 20% of cancer deaths in the United States, and as such are a major public health concern. Herein, we review and synthesize the epidemiological research regarding vitamin D, as measured by the biomarker 25-hydroxycholecalciferol [25(OH)D], and the incidence, progression, and mortality of these cancers. Overall, the results of observational studies of the relationship between 25(OH)D and colorectal cancer have revealed a consistent inverse association for incidence and mortality; while for breast cancer, results have generally demonstrated a relationship between higher 25(OH)D and lower risk for progression and mortality. In contrast, randomized, double-blind clinical trials conducted to date have generally failed to support these findings. For prostate cancer, there is no convincing evidence of an association between 25(OH)D and incidence, and inconsistent data for progression and mortality, though results of one open label clinical trial suggest that supplementation with 4000 IU/d of vitamin D3 may inhibit progression of the disease. Nonetheless, until the results of additional ongoing randomized, double-blind clinical trials are reported, it will be difficult to ascertain if vitamin D itself is related to a reduction in risk for some cancer endpoints, or whether high concentrations of the vitamin D biomarker 25(OH)D may instead serve as a marker for an overall beneficial risk factor profile.

Keywords: 25(OH)D; Vitamin D; breast cancer; colorectal cancer; prostate cancer.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interest exists.

Figures

Figure 1
Figure 1
Summary of findings from observational epidemiological studies of 25(OH)D in the carcinogenesis pathway of colorectal, breast, and prostate cancers. Solid-colored bars represent consistent evidence for protection against cancer, white bars represent no evidence, and hashed bars represent inconsistent evidence for the association between 25(OH)D and the indicated endpoints of pre-cancerous lesions and cancer incidence, progression, or mortality.

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References

    1. Siegel RL, Miller KD, Jemal A. Cancer statistics. CA: Cancer J Clin. 2015;65(1):5–29. - PubMed
    1. Siegel R, Ma J, Zou Z, Jemal A. Cancer statistics, 2014. CA: Cancer J Clin. 2014;64:9–29. - PubMed
    1. Leslie A, Carey FA, Pratt NR. et al. The colorectal adenoma-carcinoma sequence. Br J Surg. 2002;89:845–65. - PubMed
    1. Heitman SJ, Ronksley PE, Hilsden RJ. et al. Prevalence of adenomas and colorectal cancer in average risk individuals: a systematic review and meta-analysis. Clin Gastroenterol H. 2009;7:1272–8. - PubMed
    1. Winawer SJ, Zauber AG, Fletcher RH. et al. Guidelines for colonoscopy surveillance after polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer and the American Cancer Society. CA: Cancer J Clin. 2006;56:143–596. - PubMed