Erica Proctor1, Kelley M Kidwell2, Evelyn Jiagge1,3,4, Jessica Bensenhaver1,5,6, Baffour Awuah7, Kofi Gyan1, Kathy Toy8, Joseph Kwaku Oppong3, Ishmael Kyei3, Francis Aitpillah3, Ernest Osei-Bonsu7, Ernest Adjei9, Michael Ohene-Yeboah7, Robert Newman Brewer1, Linda Ahenkorah Fondjo8, Osei Owusu-Afriyie8,9, Max Wicha4,6, Sofia Merajver4,6, Celina Kleer8,6, Lisa Newman10,11,12. 1. Department of Surgery, University of Michigan, Ann Arbor, MI, USA. 2. Department of Biostatistics, University of Michigan, Ann Arbor, MI, USA. 3. Department of Surgery, Komfo Anoyke Teaching Hospital, Kumasi, Ghana. 4. Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA. 5. Division of Surgical Oncology, University of Michigan Health Systems, Ann Arbor, MI, USA. 6. Breast Care Center, University of Michigan, Comprehensive Cancer Center, Ann Arbor, MI, USA. 7. Department of Oncology, Komfo Anoyke Teaching Hospital, Kumasi, Ghana. 8. Department of Pathology, University of Michigan, Ann Arbor, MI, USA. 9. Department of Pathology, Komfo Anoyke Teaching Hospital, Kumasi, Ghana. 10. Department of Surgery, University of Michigan, Ann Arbor, MI, USA. lanewman@umich.edu. 11. Division of Surgical Oncology, University of Michigan Health Systems, Ann Arbor, MI, USA. lanewman@umich.edu. 12. Breast Care Center, University of Michigan, Comprehensive Cancer Center, Ann Arbor, MI, USA. lanewman@umich.edu.
Abstract
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 < 0.0001), but there was no association between ALDH1 and AR expression. Among the TNBC cases, 45 % were ALDH1-positive and 24 % were AR-positive. ALDH1 positivity was associated with AR positivity within the subset of TNBC (36 vs. 14 %; p = 0.019). CONCLUSION: We confirmed other studies showing a high frequency of TNBC in Africa. Surprisingly, ALDH1 was found to correlate with AR expression among TNBC, suggesting that novel TNBC subtypes may exist among populations with African ancestry.
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 < 0.0001), but there was no association between ALDH1 and AR expression. Among the TNBC cases, 45 % were ALDH1-positive and 24 % were AR-positive. ALDH1 positivity was associated with AR positivity within the subset of TNBC (36 vs. 14 %; p = 0.019). CONCLUSION: We confirmed other studies showing a high frequency of TNBC in Africa. Surprisingly, ALDH1 was found to correlate with AR expression among TNBC, suggesting that novel TNBC subtypes may exist among populations with African ancestry.
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