Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer

Abstract Bcl-2, a key regulator of cellular apoptosis, is typically linked to adverse prognosis in solid tumors due to its inhibition of apoptotic cell death and promotion of cellular proliferation, leading to tumor progression. However, studies on Bcl-2 in breast cancer have shown inconsistent resu...

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Main Authors: Taeyeong Kim, Seung Taek Lim, Hyang Suk Choi, In-Jeong Cho, Hany Noh, Jong-In Lee, Airi Han
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-024-83302-w
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author Taeyeong Kim
Seung Taek Lim
Hyang Suk Choi
In-Jeong Cho
Hany Noh
Jong-In Lee
Airi Han
author_facet Taeyeong Kim
Seung Taek Lim
Hyang Suk Choi
In-Jeong Cho
Hany Noh
Jong-In Lee
Airi Han
author_sort Taeyeong Kim
collection DOAJ
description Abstract Bcl-2, a key regulator of cellular apoptosis, is typically linked to adverse prognosis in solid tumors due to its inhibition of apoptotic cell death and promotion of cellular proliferation, leading to tumor progression. However, studies on Bcl-2 in breast cancer have shown inconsistent results, with some indicating favorable outcomes. This study aims to determine the subtype-specific role of Bcl-2 in breast cancer. Female breast cancer patients who completed primary treatment at Wonju Severance Hospital, Korea, from 2004 to 2018 were included. Clinicopathological characteristics, including Bcl-2 expression, were collected, and patients were classified based on Bcl-2 expression in more than or less than 10% of tumor cells. Kaplan–Meier curves compared recurrence-free interval (RFI) and overall survival (OS). The final cohort of 617 patients, with a mean age of 54.79 ± 11.2 years, showed no overall survival difference by Bcl-2 status (p = 0.616). In HER2-overexpressed patients, high Bcl-2 expression was linked to poor prognosis (p = 0.0021). This trend appeared in ER-positive (p = 0.297) and ER-negative (p = 0.029) subgroups. Conversely, in HER2-negative patients, Bcl-2 overexpression indicated better survival (p = 0.009), consistent in ER-positive (p = 0.259) and ER-negative (p = 0.010) subgroups. Bcl-2’s impact on survival varies with HER2 status, showing poor prognosis in HER2-overexpressed and better prognosis in HER2-negative patients.
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spelling doaj-art-470ff2872a214f5bacfcffda9a2f916e2025-01-12T12:20:19ZengNature PortfolioScientific Reports2045-23222025-01-011511810.1038/s41598-024-83302-wSubtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancerTaeyeong Kim0Seung Taek Lim1Hyang Suk Choi2In-Jeong Cho3Hany Noh4Jong-In Lee5Airi Han6Department of Pathology, Yonsei University Wonju College of MedicineDepartment of Oncology, Yonsei University Wonju College of MedicineDepartment of Surgery, Yonsei University Wonju College of MedicineDepartment of Surgery, Yonsei University Wonju College of MedicineDepartment of Surgery, Yonsei University Wonju College of MedicineDepartment of Oncology, Yonsei University Wonju College of MedicineDepartment of Surgery, Yonsei University Wonju College of MedicineAbstract Bcl-2, a key regulator of cellular apoptosis, is typically linked to adverse prognosis in solid tumors due to its inhibition of apoptotic cell death and promotion of cellular proliferation, leading to tumor progression. However, studies on Bcl-2 in breast cancer have shown inconsistent results, with some indicating favorable outcomes. This study aims to determine the subtype-specific role of Bcl-2 in breast cancer. Female breast cancer patients who completed primary treatment at Wonju Severance Hospital, Korea, from 2004 to 2018 were included. Clinicopathological characteristics, including Bcl-2 expression, were collected, and patients were classified based on Bcl-2 expression in more than or less than 10% of tumor cells. Kaplan–Meier curves compared recurrence-free interval (RFI) and overall survival (OS). The final cohort of 617 patients, with a mean age of 54.79 ± 11.2 years, showed no overall survival difference by Bcl-2 status (p = 0.616). In HER2-overexpressed patients, high Bcl-2 expression was linked to poor prognosis (p = 0.0021). This trend appeared in ER-positive (p = 0.297) and ER-negative (p = 0.029) subgroups. Conversely, in HER2-negative patients, Bcl-2 overexpression indicated better survival (p = 0.009), consistent in ER-positive (p = 0.259) and ER-negative (p = 0.010) subgroups. Bcl-2’s impact on survival varies with HER2 status, showing poor prognosis in HER2-overexpressed and better prognosis in HER2-negative patients.https://doi.org/10.1038/s41598-024-83302-wBcl-2Breast cancerHER2 statusApoptosisPrognosisTumor progression
spellingShingle Taeyeong Kim
Seung Taek Lim
Hyang Suk Choi
In-Jeong Cho
Hany Noh
Jong-In Lee
Airi Han
Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
Scientific Reports
Bcl-2
Breast cancer
HER2 status
Apoptosis
Prognosis
Tumor progression
title Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
title_full Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
title_fullStr Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
title_full_unstemmed Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
title_short Subtype-specific prognostic impact of Bcl-2 in HER2-positive and HER2-negative breast cancer
title_sort subtype specific prognostic impact of bcl 2 in her2 positive and her2 negative breast cancer
topic Bcl-2
Breast cancer
HER2 status
Apoptosis
Prognosis
Tumor progression
url https://doi.org/10.1038/s41598-024-83302-w
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