Bovine lactoferrin and lactoferrin peptides affect endometrial and cervical cancer cell lines.


Journal

Biochemistry and cell biology = Biochimie et biologie cellulaire
ISSN: 1208-6002
Titre abrégé: Biochem Cell Biol
Pays: Canada
ID NLM: 8606068

Informations de publication

Date de publication:
02 2021
Historique:
pubmed: 15 12 2020
medline: 28 8 2021
entrez: 14 12 2020
Statut: ppublish

Résumé

Cervical, uterine, and ovarian cancers are the most common malignancies of the female genital tract worldwide. Despite advances in prevention, early diagnosis, effective screening, and treatment programs, mortality remains high. Consequently, it is important to search for new treatments. The activity of bovine lactoferrin (bLF) and LF peptides against several types of cancer has been studied; however, only a few studies report the effect of bLF and LF peptides against cervical and endometrial cancers. In this study, we explored the effect of bLF as well as LF chimera and its constituent peptides LFcin17-30 and LFampin265-284 on the viability of cervical (HeLa, SiHa) and endometrial (KLE, HEC-1A) cancer cell lines. Cell proliferation was quantified with an MTT assay, cell morphological changes and damage were determined by Giemsa and phalloidin-TRITC and DAPI staining, and apoptotic and necrotic cells were identified by Alexa Fluor® 488 Annexin V and propidium iodide staining. Additionally, the effect of combinations of bLF and LF peptides with cisplatin was assessed. bLF and LF peptides inhibited the proliferation of uterine cancer cells and caused cellular morphological changes and damage to cell monolayers. bLF induced apoptosis, LFcin17-30 and LFampin265-284 induced apoptosis and necrosis, and LF chimera induced necrosis. Additionally, bLF and LF chimera showed an additive interaction with cisplatin against uterine cancer cells.

Identifiants

pubmed: 33307991
doi: 10.1139/bcb-2020-0074
doi:

Substances chimiques

Antineoplastic Agents 0
Peptide Fragments 0
Lactoferrin EC 3.4.21.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

149-158

Auteurs

Diana A Ramírez-Sánchez (DA)

CIASaP, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.
Programa Regional del Noroeste para el Doctorado en Biotecnología, Facultad de Ciencias Químico-Biológicas, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.

Izamar G Arredondo-Beltrán (IG)

CIASaP, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.
Maestría en Ciencias en Biomedicina Molecular, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.

Adrián Canizalez-Roman (A)

CIASaP, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.
Hospital de la Mujer, Servicios de Salud de Sinaloa, Culiacán Sinaloa, México.

Héctor Flores-Villaseñor (H)

CIASaP, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.

Kamran Nazmi (K)

Department of Oral Biochemistry ACTA, University of Amsterdam and VU University, Amsterdam, the Netherlands.

Jan G M Bolscher (JGM)

Department of Oral Biochemistry ACTA, University of Amsterdam and VU University, Amsterdam, the Netherlands.

Nidia León-Sicairos (N)

CIASaP, Facultad de Medicina, Universidad Autónoma de Sinaloa, Culiacán Sinaloa, México.
Departamento de Investigación del Hospital Pediátrico, Servicios de Salud de Sinaloa, Culiacán Sinaloa, México.

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Classifications MeSH