Bovine lactoferrin and lactoferrin peptides affect endometrial and cervical cancer cell lines.
Animals
Antineoplastic Agents
/ administration & dosage
Cattle
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Cells, Cultured
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
Endometrial Neoplasms
/ drug therapy
Female
Lactoferrin
/ administration & dosage
Peptide Fragments
/ administration & dosage
Uterine Cervical Neoplasms
/ drug therapy
apoptose
apoptosis
cancer
lactoferrin
lactoferrin peptides
lactoferrine
peptides de la lactoferrine
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
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