“…Four-micrometer-thick, formalin-fixed, paraffin-embedded sections were deparaffinized and rehydrated using xylene and alcohol solutions. Immunostaining was performed using automated instruments [7,16,[21][22][23][24][25][26][27]. After antigen retrieval, the sections were incubated with primary antibodies against paired box 8 (PAX8, 1:50, polyclonal, Cell Marque, Rocklin, CA, USA), PAX2 (1:100, polyclonal, Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA), GATA-binding protein 3 (GATA3, 1:400, clone L50-823, Cell Marque), Wilms tumor 1 (WT1, 1:800, clone 6F-H2, Cell Marque), estrogen receptor (ER, 1:150, clone 6F11, Novocastra, Leica Biosystems, Newcastle Upon Tyne, UK), progesterone receptor (PR, 1:100, clone 16, Novocastra), p16 (prediluted, clone E6H4, Ventana Medical Systems), p53 (1:300, clone DO-7, Novocastra), and phosphatase and tensin homolog deleted on chromosome 10 (PTEN, prediluted, clone SP218, Ventana Medical Systems).…”