Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2009;61(5):708-16.
doi: 10.1080/01635580902913047.

Soy consumption and histopathologic markers in breast tissue using tissue microarrays

Affiliations

Soy consumption and histopathologic markers in breast tissue using tissue microarrays

Gertraud Maskarinec et al. Nutr Cancer. 2009.

Abstract

This study examined the relation of soy intake with hormonal and proliferation markers in benign and malignant breast tissue using tissue microarrays (TMAs). TMAs with up to 4 malignant and 4 benign tissue samples for 268 breast cancer cases were constructed. Soy intake in early life and in adulthood was assessed by questionnaire. The TMAs were stained for estrogen receptor (ER) alpha, ERbeta, progesterone receptor (PR), human epidermal growth factor receptor 2 (HER2/neu), proliferating cell nuclear antigen (PCNA), and Ki-67 using standard immunohistochemical methods. Logistic regression was applied for statistical analysis. A higher percentage of women showed positive marker expression in malignant than in benign tissue. With one exception, HER2/neu, no significant associations between soy intake and pathologic markers were observed. Early life soy intake was associated with lower HER2/neu and PCNA staining of malignant tissue. In benign tissue, early life soy intake showed higher ER and PR expression, but no difference in proliferation markers. The results of this investigation provide some assurance that soy intake does not adversely affect markers of proliferation. TMAs were shown to be a useful tool for epidemiologic research.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Representative photomicrographs of benign tissue (top row) and malignant tissue (bottom row).
Figure 2
Figure 2
Percent of women by ethnicity and positive marker expression in malignant and benign tissue* *Positive = ≥10% stain or ERα, ERβ, HER2/neu, and PCNA; any stain for PR and Ki-67

References

    1. Trock BJ, Hilakivi-Clarke L, Clarke R. Meta-analysis of soy intake and breast cancer risk. J Natl Cancer Inst. 2006;98:459–471. - PubMed
    1. Wu AH, Yu MC, Tseng CC, Pike MC. Epidemiology of soy exposures and breast cancer risk. Br J Cancer. 2008;98:9–14. - PMC - PubMed
    1. Henderson BE, Pike MC, Bernstein L, Ross RK. In: Breast cancer. Schottenfeld D, editor. Oxford University Press; New York: 1996. pp. 1022–1039.
    1. Russo J, Hu YF, Yang X, Russo IH. Developmental, cellular, and molecular basis of human breast cancer. J Natl Cancer Inst Monogr. 2000:17–37. - PubMed
    1. Guzman RC, Yang J, Rajkumar L, Thordarson G, Chen X, et al. Hormonal prevention of breast cancer: mimicking the protective effect of pregnancy. Proc Natl Acad Sci U S A. 1999;96:2520–2525. - PMC - PubMed

Publication types

MeSH terms