Expression of autophagy-related markers beclin-1, light chain 3A, light chain 3B and p62 according to the molecular subtype of breast cancer

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Abstract

Aims: To investigate the relationship between the expression of autophagy-related proteins, including beclin-1, light chain (LC) 3A, LC3B, and p62, and prognosis in invasive breast cancer. Methods and results: We constructed tissue microarrays from the breast cancer cells of 489 patients, and classified molecular subtypes using surrogate immunohistochemical stains. The tumoral expression levels of LC3A and LC3B were highest in triple-negative breast cancer (TNBC) (P<0.001), whereas these types of tumour had the lowest expression levels of these markers in the stroma (P=0.005 and P<0.001, respectively). Cytoplasmic beclin-1 expression was highest in TNBC, but nuclear expression was lowest (P<0.001). p62 cytoplasmic and nuclear expression were highest in HER2-type tumours (P=0.001 and P<0.001, respectively). Tumoral LC3A and LC3B expression were associated with high histological grade (P<0.001, and P<0.028, respectively), but nuclear p62 expression was associated with lower histological grade (P=0.004). Conclusions: Autophagy-related markers are differentially expressed according to the molecular subtype of breast cancer. In particular, expression of LC3A, LC3B and beclin-1 was highest in TNBC tumour cells, whereas that of LC3A and LC3B in the tumour stroma was lowest in TNBC.

Original languageEnglish
Pages (from-to)275-286
Number of pages12
JournalHistopathology
Volume62
Issue number2
DOIs
Publication statusPublished - 2013 Jan 1

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Triple Negative Breast Neoplasms
Autophagy
Breast Neoplasms
Light
Neoplasms
Coloring Agents
Beclin-1

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Histology

Cite this

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title = "Expression of autophagy-related markers beclin-1, light chain 3A, light chain 3B and p62 according to the molecular subtype of breast cancer",
abstract = "Aims: To investigate the relationship between the expression of autophagy-related proteins, including beclin-1, light chain (LC) 3A, LC3B, and p62, and prognosis in invasive breast cancer. Methods and results: We constructed tissue microarrays from the breast cancer cells of 489 patients, and classified molecular subtypes using surrogate immunohistochemical stains. The tumoral expression levels of LC3A and LC3B were highest in triple-negative breast cancer (TNBC) (P<0.001), whereas these types of tumour had the lowest expression levels of these markers in the stroma (P=0.005 and P<0.001, respectively). Cytoplasmic beclin-1 expression was highest in TNBC, but nuclear expression was lowest (P<0.001). p62 cytoplasmic and nuclear expression were highest in HER2-type tumours (P=0.001 and P<0.001, respectively). Tumoral LC3A and LC3B expression were associated with high histological grade (P<0.001, and P<0.028, respectively), but nuclear p62 expression was associated with lower histological grade (P=0.004). Conclusions: Autophagy-related markers are differentially expressed according to the molecular subtype of breast cancer. In particular, expression of LC3A, LC3B and beclin-1 was highest in TNBC tumour cells, whereas that of LC3A and LC3B in the tumour stroma was lowest in TNBC.",
author = "Junjeong Choi and Woohee Jung and Koo, {Ja Seung}",
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T1 - Expression of autophagy-related markers beclin-1, light chain 3A, light chain 3B and p62 according to the molecular subtype of breast cancer

AU - Choi, Junjeong

AU - Jung, Woohee

AU - Koo, Ja Seung

PY - 2013/1/1

Y1 - 2013/1/1

N2 - Aims: To investigate the relationship between the expression of autophagy-related proteins, including beclin-1, light chain (LC) 3A, LC3B, and p62, and prognosis in invasive breast cancer. Methods and results: We constructed tissue microarrays from the breast cancer cells of 489 patients, and classified molecular subtypes using surrogate immunohistochemical stains. The tumoral expression levels of LC3A and LC3B were highest in triple-negative breast cancer (TNBC) (P<0.001), whereas these types of tumour had the lowest expression levels of these markers in the stroma (P=0.005 and P<0.001, respectively). Cytoplasmic beclin-1 expression was highest in TNBC, but nuclear expression was lowest (P<0.001). p62 cytoplasmic and nuclear expression were highest in HER2-type tumours (P=0.001 and P<0.001, respectively). Tumoral LC3A and LC3B expression were associated with high histological grade (P<0.001, and P<0.028, respectively), but nuclear p62 expression was associated with lower histological grade (P=0.004). Conclusions: Autophagy-related markers are differentially expressed according to the molecular subtype of breast cancer. In particular, expression of LC3A, LC3B and beclin-1 was highest in TNBC tumour cells, whereas that of LC3A and LC3B in the tumour stroma was lowest in TNBC.

AB - Aims: To investigate the relationship between the expression of autophagy-related proteins, including beclin-1, light chain (LC) 3A, LC3B, and p62, and prognosis in invasive breast cancer. Methods and results: We constructed tissue microarrays from the breast cancer cells of 489 patients, and classified molecular subtypes using surrogate immunohistochemical stains. The tumoral expression levels of LC3A and LC3B were highest in triple-negative breast cancer (TNBC) (P<0.001), whereas these types of tumour had the lowest expression levels of these markers in the stroma (P=0.005 and P<0.001, respectively). Cytoplasmic beclin-1 expression was highest in TNBC, but nuclear expression was lowest (P<0.001). p62 cytoplasmic and nuclear expression were highest in HER2-type tumours (P=0.001 and P<0.001, respectively). Tumoral LC3A and LC3B expression were associated with high histological grade (P<0.001, and P<0.028, respectively), but nuclear p62 expression was associated with lower histological grade (P=0.004). Conclusions: Autophagy-related markers are differentially expressed according to the molecular subtype of breast cancer. In particular, expression of LC3A, LC3B and beclin-1 was highest in TNBC tumour cells, whereas that of LC3A and LC3B in the tumour stroma was lowest in TNBC.

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