Clinical significance of sHER2‑ECD and calpain‑10 expression in tumor tissues of patients with breast cancer.


Journal

Oncology reports
ISSN: 1791-2431
Titre abrégé: Oncol Rep
Pays: Greece
ID NLM: 9422756

Informations de publication

Date de publication:
06 2020
Historique:
received: 08 06 2019
accepted: 26 02 2020
pubmed: 3 4 2020
medline: 21 10 2020
entrez: 3 4 2020
Statut: ppublish

Résumé

Human epidermal growth factor receptor 2 (HER2) is composed of an extracellular domain (ECD), a lipophilic transmembrane region and an intracellular domain (ICD). The most commonly used method to determine the status of HER2 is immunohistochemistry. However, false‑negative results are sometimes given, which causes some patients to lose the opportunity for anti‑HER2 therapy. We found that calpain‑10 may prohibit HER2‑ECD into peripheral blood resulting in a HER2‑negative result by the immunohistochemical method. We enrolled 289 patients into our experiment to assess the relationship between sHER2‑ECD and calpain‑10. The results showed that there was a positive correlation between sHER2‑ECD and calpain‑10. Moreover, we also investigated the prognostic values of sHER2‑ECD and calpain‑10 in breast cancer patients. According to the follow‑up results, positive sHER2‑ECD and tissue calpain‑10 were indicative of a poor prognosis in breast cancer patients. Subsequently, we further validated the relationship between the two molecules in in vitro experiments. In the in vitro experiments, the level of HER2‑ECD in the culture medium was increased or decreased with a decrease or increase in calpain‑10 by transfection technology, showing an inverse association. The results indicated that sHER2‑ECD and tissue calpain‑10 levels were powerful factors to assess the status of HER2. In combination with tissue HER2 detection, the occurrence of false‑negative HER2 was reduced, providing patients with additional treatment opportunities. In conclusion, sHER2‑ECD and tissue calpain‑10 may be used as new prognostic indices for breast cancer.

Identifiants

pubmed: 32236617
doi: 10.3892/or.2020.7564
doi:

Substances chimiques

Biomarkers, Tumor 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1
Calpain EC 3.4.22.-
calpain 10 EC 3.4.22.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2093-2104

Auteurs

Yawen Ding (Y)

Clinical Laboratory, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Ming Ma (M)

Clinical Laboratory, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Qingjing Li (Q)

Clinical Laboratory, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Shejun Gao (S)

Clinical Laboratory, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Sainan Li (S)

Breast Center, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Junying Liu (J)

Department of Pathology, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

Cuizhi Geng (C)

Breast Center, The Fourth Hospital of Hebei Medical University, Shiljiazhuang, Hebei 050011, P.R. China.

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Classifications MeSH