TY - JOUR
T1 - Tissue-based associations of mammographic breast density with breast stem cell markers
AU - Yaghjyan, Lusine
AU - Stoll, Ethan
AU - Ghosh, Karthik
AU - Scott, Christopher G.
AU - Jensen, Matthew R.
AU - Brandt, Kathleen R.
AU - Visscher, Daniel
AU - Vachon, Celine M.
N1 - Funding Information:
This work was supported by the University of Florida Cancer Center through the Florida Consortium of National Cancer Institute Centers Program at the University of Florida (Bridge Funding to LY); Mayo Clinic CCaTS KL2 program (K12 RR24151); and Mayo Clinic Breast SPORE (NCI P50 CA116201; NCI R01 CA128931; NCI R01 CA140286).
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/8/29
Y1 - 2017/8/29
N2 - Background: Mammographic breast density is a well-established, strong breast cancer risk factor but the biology underlying this association remains unclear. Breast density may reflect underlying alterations in the size and activity of the breast stem cell pool. We examined, for the first time, associations of CD44, CD24, and aldehyde dehydrogenase family 1 member A1 (ALDH1A1) breast stem cell markers with breast density. Methods: We included in this study 64 asymptomatic healthy women who previously volunteered for a unique biopsy study of normal breast tissue at the Mayo Clinic (2006-2008). Mammographically identified dense and non-dense areas were confirmed/localized by ultrasound and biopsied. Immunohistochemical analysis of the markers was performed according to a standard protocol and the staining was assessed by a single blinded pathologist. In core biopsy samples retrieved from areas of high vs. low density within the same woman, we compared staining extent and an expression score (the product of staining intensity and extent), using the signed rank test. All tests of statistical significance were two-sided. Results: A total of 64, 28, and 10 women were available for CD44, CD24, and ALDH1A1 staining, respectively. For all three markers, we found higher levels of staining extent in dense as compared to non-dense tissue, though for CD24 and ALDH1A1 the difference did not reach statistical significance (CD44, 6.3% vs. 2.0%, p<0.001; CD24, 8.0% vs. 5.6%, p=0.10; and ALDH1A1, 0.5% vs. 0.3%, p=0.12). The expression score for CD44 was significantly greater in dense as compared to non-dense tissue (9.8 vs.3.0, p<0.001). Conclusions: Our findings suggest an increased presence and/or activity of stem cells in dense as compared to non-dense breast tissue.
AB - Background: Mammographic breast density is a well-established, strong breast cancer risk factor but the biology underlying this association remains unclear. Breast density may reflect underlying alterations in the size and activity of the breast stem cell pool. We examined, for the first time, associations of CD44, CD24, and aldehyde dehydrogenase family 1 member A1 (ALDH1A1) breast stem cell markers with breast density. Methods: We included in this study 64 asymptomatic healthy women who previously volunteered for a unique biopsy study of normal breast tissue at the Mayo Clinic (2006-2008). Mammographically identified dense and non-dense areas were confirmed/localized by ultrasound and biopsied. Immunohistochemical analysis of the markers was performed according to a standard protocol and the staining was assessed by a single blinded pathologist. In core biopsy samples retrieved from areas of high vs. low density within the same woman, we compared staining extent and an expression score (the product of staining intensity and extent), using the signed rank test. All tests of statistical significance were two-sided. Results: A total of 64, 28, and 10 women were available for CD44, CD24, and ALDH1A1 staining, respectively. For all three markers, we found higher levels of staining extent in dense as compared to non-dense tissue, though for CD24 and ALDH1A1 the difference did not reach statistical significance (CD44, 6.3% vs. 2.0%, p<0.001; CD24, 8.0% vs. 5.6%, p=0.10; and ALDH1A1, 0.5% vs. 0.3%, p=0.12). The expression score for CD44 was significantly greater in dense as compared to non-dense tissue (9.8 vs.3.0, p<0.001). Conclusions: Our findings suggest an increased presence and/or activity of stem cells in dense as compared to non-dense breast tissue.
KW - Breast cancer risk
KW - Breast density
KW - Immunohistochemistry
KW - Staining extent
KW - Stem cell markers
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U2 - 10.1186/s13058-017-0889-3
DO - 10.1186/s13058-017-0889-3
M3 - Article
C2 - 28851411
AN - SCOPUS:85028507127
SN - 1465-5411
VL - 19
JO - Breast Cancer Research
JF - Breast Cancer Research
IS - 1
M1 - 100
ER -