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Abstract Background: PAM50, a 50-gene signature, classifies breast cancers into one of five subtypes (basal, luminal A, luminal B, HER2-enriched, and normal-like), revealing information about underlying tumor biology, and has emerged as a key prognostic indicator influencing treatment decisions. There is growing interest in bridging the gap between expression-based metrics and histopathology, where immunohistochemistry (IHC) and sequencing-based approaches have been proposed for this purpose. However, hematoxylin and eosin (H 2023 Dec 5-9; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2024;84(9 Suppl):Abstract nr PO3-07-04.
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Guramare et al. (Thu,) studied this question.
www.synapsesocial.com/papers/68e6be8eb6db64358763e3cc — DOI: https://doi.org/10.1158/1538-7445.sabcs23-po3-07-04
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
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