“…Currently, the classification and assessment of BC primarily rely on tumor staging, grading, and several molecular biomarkers, including estrogen receptor (ER), progesterone receptor (PgR), human epidermal growth factor receptor 2 (HER2), and K i -67 (a proliferation marker). Based on the expression of these markers, BC is categorized into four primary subtypes, each with distinct prognoses and outcomes: luminal A (ER+, PR+, HER2–, low K i -67), luminal B (ER+, PR±, HER2±, high K i -67), HER2 overexpression (ER–, PR–, HER2+), and triple-negative (TNBC/ER–, PR–, HER2−) . Around 40–50% of BCs are of the Luminal A subtype, while Luminal B, HER2 overexpression, and triple-negative frequencies are approximately 20–30, 15–20, and 10–20%, respectively .…”