Differences in cysteine peptidases-like activity in sera of patients with breast cancer.


Journal

Cancer biomarkers : section A of Disease markers
ISSN: 1875-8592
Titre abrégé: Cancer Biomark
Pays: Netherlands
ID NLM: 101256509

Informations de publication

Date de publication:
2020
Historique:
pubmed: 7 11 2019
medline: 21 11 2020
entrez: 6 11 2019
Statut: ppublish

Résumé

The key role in carcinogenesis with destruction of the extracellular matrix is played by proteases released by invasive cancer cells. Cysteine peptidases, such as cathepsin B and L, take an important role in cancer progression and metastasis. Cysteine peptidase-like activity (CPA) in sera of patients with breast cancer at different stages of disease and the influence of genetic predisposition associated with BRCA-1 gene mutations were analysed. CPA in serum was determined with the spectrofluorometric technique using Z-Phe-Arg-AMC as a substrate. Determination was carried out in 111 breast cancer patients in comparison to a control group of 50 healthy subjects. The highest CPA was found in breast cancer patients with a hereditary predisposition bearing BRCA1 gene mutations, and the lowest activity was found in patients who had a tumour surgically removed and before adjuvant therapy. The differences in the activities between control group and cancer groups were statistically significant (p< 0.05), except from group of cancer patients in complete remission (p< 0.52). Serum CPA in patients with breast cancer differs depending on the cancer stage and treatment methods. Our study demonstrate the correlation between BRCA-1 gene mutations and the increased level of CPA.

Sections du résumé

BACKGROUND BACKGROUND
The key role in carcinogenesis with destruction of the extracellular matrix is played by proteases released by invasive cancer cells. Cysteine peptidases, such as cathepsin B and L, take an important role in cancer progression and metastasis.
OBJECTIVES OBJECTIVE
Cysteine peptidase-like activity (CPA) in sera of patients with breast cancer at different stages of disease and the influence of genetic predisposition associated with BRCA-1 gene mutations were analysed.
METHODS METHODS
CPA in serum was determined with the spectrofluorometric technique using Z-Phe-Arg-AMC as a substrate. Determination was carried out in 111 breast cancer patients in comparison to a control group of 50 healthy subjects.
RESULTS RESULTS
The highest CPA was found in breast cancer patients with a hereditary predisposition bearing BRCA1 gene mutations, and the lowest activity was found in patients who had a tumour surgically removed and before adjuvant therapy. The differences in the activities between control group and cancer groups were statistically significant (p< 0.05), except from group of cancer patients in complete remission (p< 0.52).
CONCLUSIONS CONCLUSIONS
Serum CPA in patients with breast cancer differs depending on the cancer stage and treatment methods. Our study demonstrate the correlation between BRCA-1 gene mutations and the increased level of CPA.

Identifiants

pubmed: 31683457
pii: CBM190327
doi: 10.3233/CBM-190327
doi:

Substances chimiques

BRCA1 Protein 0
BRCA1 protein, human 0
Cysteine Endopeptidases EC 3.4.22.-

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

335-341

Auteurs

Ewa Kilar (E)

Department of Oncology, District Hospital, Swidnica, Poland.

Maciej Siewiński (M)

Department of Basic Sciences, Wroclaw Medical University, Wroclaw, Poland.

Lidia Hirnle (L)

1st Department and Clinic of Gynaecology and Obstetrics, Wrocław Medical University, Wroclaw, Poland.

Teresa Skiba (T)

Department of Animal Product Technology and Quality Management, Wroclaw University of Environmental and Life Sciences, Wroclaw, Poland.

Krzysztof Goła B (K)

Department of Pharmaceutical Biochemistry, Wroclaw Medical University, Wroclaw, Poland.

Jakub Gburek (J)

Department of Pharmaceutical Biochemistry, Wroclaw Medical University, Wroclaw, Poland.

Marek Murawski (M)

1st Department and Clinic of Gynaecology and Obstetrics, Wrocław Medical University, Wroclaw, Poland.

Anna Janocha (A)

Department of Pathophysiology, Wroclaw Medical University, Wroclaw, Poland.

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Classifications MeSH