TY - JOUR
T1 - Expression of Androgen Receptor and Cancer Stem Cell Markers (CD44+/CD24− and ALDH1+)
T2 - Prognostic Implications in Invasive Breast Cancer
AU - Riaz, Nazia
AU - Idress, Romana
AU - Habib, Sadia
AU - Azam, Iqbal
AU - Lalani, El Nasir MA
N1 - Publisher Copyright:
© 2018 The Authors
PY - 2018/8
Y1 - 2018/8
N2 - BACKGROUND: Androgen receptor (AR) has emerged as a significant prognostic marker in early breast cancer (BCa). Association of AR with cancer stem cell (CSC) markers in BCa is unknown. Aim of the present study was to evaluate the immunohistochemical expression of AR, CD44, CD24 and ALDH1 in a cohort of Pakistani patients diagnosed with invasive BCa and to correlate the expression with 5- year disease free survival. PATIENTS AND METHODS: We evaluated immunohistochemical expression AR, CD44, CD24 and ALDH1 in formalin fixed paraffin embedded archival blocks of 166 cases of primary invasive BCa (stage I-III) and correlated the expression with clinicopathological variables and outcome using univariable and multivariable analysis. Survival data was computed by Kaplan Meier curves. RESULTS: Expression of AR was observed in 62.7% tumors whereas CD44, CD24 and ALDH1 were expressed in 61.4%, 44% and 30.1% tumors, respectively. AR expression was significantly associated with T1-T2 tumors, lower grade, estrogen and progesterone receptor expression (P <.05) and remained an independent prognostic indicator in multivariable analysis (adjusted HR 0.33, 95% CI 0.13–0.81; P =.016). Significant association was observed between concordant expression of AR and CD24 (P =.001) with a favorable impact on survival (P =.007) whereas expression of CSC phenotypes (CD44+, CD44+/CD24− and ALDH1+) did not correlate with adverse outcome (P >.05). However, AR expression retained the association with better prognosis even in patients whose tumors exhibited a CSC phenotype. CONCLUSIONS: Expression of AR and CD24 in stage I-III invasive BCa correlates with favorable clinicopathological features and delineates a subgroup of patients with better disease-free survival.
AB - BACKGROUND: Androgen receptor (AR) has emerged as a significant prognostic marker in early breast cancer (BCa). Association of AR with cancer stem cell (CSC) markers in BCa is unknown. Aim of the present study was to evaluate the immunohistochemical expression of AR, CD44, CD24 and ALDH1 in a cohort of Pakistani patients diagnosed with invasive BCa and to correlate the expression with 5- year disease free survival. PATIENTS AND METHODS: We evaluated immunohistochemical expression AR, CD44, CD24 and ALDH1 in formalin fixed paraffin embedded archival blocks of 166 cases of primary invasive BCa (stage I-III) and correlated the expression with clinicopathological variables and outcome using univariable and multivariable analysis. Survival data was computed by Kaplan Meier curves. RESULTS: Expression of AR was observed in 62.7% tumors whereas CD44, CD24 and ALDH1 were expressed in 61.4%, 44% and 30.1% tumors, respectively. AR expression was significantly associated with T1-T2 tumors, lower grade, estrogen and progesterone receptor expression (P <.05) and remained an independent prognostic indicator in multivariable analysis (adjusted HR 0.33, 95% CI 0.13–0.81; P =.016). Significant association was observed between concordant expression of AR and CD24 (P =.001) with a favorable impact on survival (P =.007) whereas expression of CSC phenotypes (CD44+, CD44+/CD24− and ALDH1+) did not correlate with adverse outcome (P >.05). However, AR expression retained the association with better prognosis even in patients whose tumors exhibited a CSC phenotype. CONCLUSIONS: Expression of AR and CD24 in stage I-III invasive BCa correlates with favorable clinicopathological features and delineates a subgroup of patients with better disease-free survival.
UR - http://www.scopus.com/inward/record.url?scp=85047474287&partnerID=8YFLogxK
U2 - 10.1016/j.tranon.2018.05.002
DO - 10.1016/j.tranon.2018.05.002
M3 - Article
AN - SCOPUS:85047474287
SN - 1936-5233
VL - 11
SP - 920
EP - 929
JO - Translational Oncology
JF - Translational Oncology
IS - 4
ER -