TRPS1 is a promising marker for all subtypes of breast cancer

Author:

Lui Joshua W1,Tsang Julia Y1,Li Joshua1ORCID,Ko Chun‐Wai1,Tam Fiona2,Loong Thomson C‐W3,Tse Gary M1ORCID

Affiliation:

1. Department of Anatomical and Cellular Pathology and State Key Laboratory of Translational Oncology Prince of Wales Hospital, The Chinese University of Hong Kong Hong Kong China

2. Department of Pathology Kwong Wah Hospital Hong Kong China

3. Department of Pathology Tuen Mun Hospital Hong Kong China

Abstract

AimsTrichorhinophalangeal syndrome‐1 (TRPS1) has been proposed as a novel breast marker with equally high expression in breast cancer (BC) subtypes, making it a useful diagnostic tool. Here, its expression was evaluated alongside other commonly used markers [GATA3, GCDFP15, mammaglobin (MGB) and SOX10] in a large cohort of BCs (n = 1852) and their corresponding nodal metastases. Its usefulness as a diagnostic tool and its correlation with clinicopathological features were assessed.Methods and resultsTRPS1 was expressed at 75.8% overall in the BC cohort, with at least 58% expression among BC subtypes. It was less sensitive than GATA3 for luminal and HER2‐overexpressing (HER2‐OE) cancers (luminal A: 82 versus 97%; luminal B: 80 versus 95%; HER2‐OE: 62 versus 76%), but it was the most sensitive for TNBC (60 versus ≤ 41%). It showed a stable expression in nodal metastases (primary tumour 76 versus nodal metastasis 78%), unlike a reduced nodal expression for GATA3 (86 versus 77%). TRPS1 outperformed GATA3 in detecting non‐luminal cancers when paired with other breast markers. TRPS1 and GCDFP15 was the most sensitive combination in TNBC detection, with a 76% detection rate. For TRPS1‐negative and GCDFP15‐negative TNBCs, SOX10 was more sensitive than GATA3 (29 versus 24%).ConclusionsTRPS1 is a highly sensitive marker for all breast cancer subtypes, outperforming GATA3 in non‐luminal cancers and displaying the highest sensitivity for TNBC detection when combined with GCDFP15. It is a valuable addition to the breast marker panel for accurate identification of BC.

Funder

Health and Medical Research Fund

Chinese University of Hong Kong

Publisher

Wiley

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