Characterizing Breast Cancer in a Population with Increased Prevalence of Triple-Negative Breast Cancer: Androgen Receptor and ALDH1 Expression in Ghanaian Women

Background The androgen receptor (AR) is a commonly-expressed hormone receptor in breast cancer and may be a marker of response to targeted anti-androgen therapy, a particularly attractive option for triple-negative breast cancer (TNBC). Gene expression studies suggest that ARs may distinguish a lum...

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Veröffentlicht in:Annals of surgical oncology 2015-11, Vol.22 (12), p.3831-3835
Hauptverfasser: Proctor, Erica, Kidwell, Kelley M., Jiagge, Evelyn, Bensenhaver, Jessica, Awuah, Baffour, Gyan, Kofi, Toy, Kathy, Oppong, Joseph Kwaku, Kyei, Ishmael, Aitpillah, Francis, Osei-Bonsu, Ernest, Adjei, Ernest, Ohene-Yeboah, Michael, Brewer, Robert Newman, Fondjo, Linda Ahenkorah, Owusu-Afriyie, Osei, Wicha, Max, Merajver, Sofia, Kleer, Celina, Newman, Lisa
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Sprache:eng
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Zusammenfassung:Background The androgen receptor (AR) is a commonly-expressed hormone receptor in breast cancer and may be a marker of response to targeted anti-androgen therapy, a particularly attractive option for triple-negative breast cancer (TNBC). Gene expression studies suggest that ARs may distinguish a luminal/AR TNBC subtype from stem cell-like subtypes. TNBC frequency is two to three times higher in African American and African breast cancers compared with White American and European breast cancers, yet little is known regarding TNBC subtypes in high-frequency African-ancestry populations. We evaluated ARs and the mammary stem cell marker aldehyde dehydrogenase 1 (ALDH1) among breast cancers from Ghana, Africa. Methods Overall, 147 formalin-fixed, paraffin-embedded invasive breast cancers from the Komfo Anoyke Teaching Hospital in Ghana were studied at the University of Michigan, and analyzed immunohistochemically for estrogen receptor (ER), progesterone receptor (PR), HER2/ neu , ALDH1, and AR expression. Results The median age of patients was 45 years. Only 31 cases (21 %) were ER-positive, and 14 (10 %) were HER2-positive; 89 (61 %) were TNBCs. For the entire group, 44 % were AR-positive and 45 % were ALDH1-positive. ER/PR-positive tumors were more likely to be AR-positive compared with ER/PR-negative tumors (87 vs. 26 %; p  
ISSN:1068-9265
1534-4681
DOI:10.1245/s10434-015-4455-x