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Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment

BACKGROUND: HER2-low cancers are heterogeneous with different degrees of HER2 expression and hormone receptor (HR) status. Currently, its analysis is mostly focused on the standard clinic-pathologic features or common biomarkers expression, without considering the heterogeneity within the category....

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Autores principales: Li, Yuyang, Tsang, Julia Y., Tam, Fiona, Loong, Thomson, Tse, Gary M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130469/
https://www.ncbi.nlm.nih.gov/pubmed/37068349
http://dx.doi.org/10.1016/j.ebiom.2023.104571
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author Li, Yuyang
Tsang, Julia Y.
Tam, Fiona
Loong, Thomson
Tse, Gary M.
author_facet Li, Yuyang
Tsang, Julia Y.
Tam, Fiona
Loong, Thomson
Tse, Gary M.
author_sort Li, Yuyang
collection PubMed
description BACKGROUND: HER2-low cancers are heterogeneous with different degrees of HER2 expression and hormone receptor (HR) status. Currently, its analysis is mostly focused on the standard clinic-pathologic features or common biomarkers expression, without considering the heterogeneity within the category. A further characterization and understanding of this cancer subgroup will facilitate its management. METHODS: A large cohort of HER2-negative cancers (N = 1464) was included. The HER2-low (N = 412) and HER2-zero cancers (N = 1052) were compared and correlated with a comprehensive panel of clinico-pathologic features and biomarker expression according to different HER2 expressions and HR statuses. The prognostic values of these features in HER2-low cancers were also evaluated. FINDINGS: The characteristics of HER2-low breast cancers, as compared to HER2-zero, varied with the HR status. HER2-low luminal cancers were associated with younger age, larger tumor, high pAKT and high HLA expression. Among TNBCs, opposite trends in age and tumor size were found. Additionally, HER2-low TNBC showed less necrosis, higher pN, lower c-kit and CK14 than HER2-zero cancers. Nonetheless, regardless of HR status, HER2-low status was associated with increased COX2 and AR expression, implicated in the biology of HER2-low cancers. HER2-low cancers showed high expression of HLAs in tumors and PD-L1 in immune cells. In particular, the co-expression of HLAs was found to be associated with better survival in HER2-low cancers. INTERPRETATION: This study revealed further characteristic of HER2-low breast cancers as compared to HER2-zero cancers, provided further insights into its prognostication and therapeutic strategies. FUNDING: 10.13039/501100005847Health and Medical Research Fund (08190586), Cheng Yue Pui Charity Foundation and 10.13039/501100004853CUHK direct grant.
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spelling pubmed-101304692023-04-27 Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment Li, Yuyang Tsang, Julia Y. Tam, Fiona Loong, Thomson Tse, Gary M. eBioMedicine Articles BACKGROUND: HER2-low cancers are heterogeneous with different degrees of HER2 expression and hormone receptor (HR) status. Currently, its analysis is mostly focused on the standard clinic-pathologic features or common biomarkers expression, without considering the heterogeneity within the category. A further characterization and understanding of this cancer subgroup will facilitate its management. METHODS: A large cohort of HER2-negative cancers (N = 1464) was included. The HER2-low (N = 412) and HER2-zero cancers (N = 1052) were compared and correlated with a comprehensive panel of clinico-pathologic features and biomarker expression according to different HER2 expressions and HR statuses. The prognostic values of these features in HER2-low cancers were also evaluated. FINDINGS: The characteristics of HER2-low breast cancers, as compared to HER2-zero, varied with the HR status. HER2-low luminal cancers were associated with younger age, larger tumor, high pAKT and high HLA expression. Among TNBCs, opposite trends in age and tumor size were found. Additionally, HER2-low TNBC showed less necrosis, higher pN, lower c-kit and CK14 than HER2-zero cancers. Nonetheless, regardless of HR status, HER2-low status was associated with increased COX2 and AR expression, implicated in the biology of HER2-low cancers. HER2-low cancers showed high expression of HLAs in tumors and PD-L1 in immune cells. In particular, the co-expression of HLAs was found to be associated with better survival in HER2-low cancers. INTERPRETATION: This study revealed further characteristic of HER2-low breast cancers as compared to HER2-zero cancers, provided further insights into its prognostication and therapeutic strategies. FUNDING: 10.13039/501100005847Health and Medical Research Fund (08190586), Cheng Yue Pui Charity Foundation and 10.13039/501100004853CUHK direct grant. Elsevier 2023-04-15 /pmc/articles/PMC10130469/ /pubmed/37068349 http://dx.doi.org/10.1016/j.ebiom.2023.104571 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Articles
Li, Yuyang
Tsang, Julia Y.
Tam, Fiona
Loong, Thomson
Tse, Gary M.
Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title_full Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title_fullStr Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title_full_unstemmed Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title_short Comprehensive characterization of HER2-low breast cancers: implications in prognosis and treatment
title_sort comprehensive characterization of her2-low breast cancers: implications in prognosis and treatment
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130469/
https://www.ncbi.nlm.nih.gov/pubmed/37068349
http://dx.doi.org/10.1016/j.ebiom.2023.104571
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