Bradykinin and Neurotensin Analogues as Potential Compounds in Colon Cancer Therapy.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
01 Jun 2023
Historique:
received: 31 03 2023
revised: 29 05 2023
accepted: 30 05 2023
medline: 12 6 2023
pubmed: 10 6 2023
entrez: 10 6 2023
Statut: epublish

Résumé

Colorectal cancer (CRC) is one of the most lethal malignancies worldwide, so the attempts to find novel therapeutic approaches are necessary. The aim of our study was to analyze how chemical modifications influence physical, chemical, and biological properties of the two peptides, namely, bradykinin (BK) and neurotensin (NT). For this purpose, we used fourteen modified peptides, and their anti-cancers features were analyzed on the HCT116 CRC cell line. Our results confirmed that the spherical mode of a CRC cell line culture better reflects the natural tumour microenvironment. We observed that the size of the colonospheres was markedly reduced following treatment with some BK and NT analogues. The proportion of CD133+ cancer stem cells (CSCs) in colonospheres decreased following incubation with the aforementioned peptides. In our research, we found two groups of these peptides. The first group influenced all the analyzed cellular features, while the second seemed to include the most promising peptides that lowered the count of CD133+ CSCs with parallel substantial reduction in CRC cells viability. These analogues need further analysis to uncover their overall anti-cancer potential.

Identifiants

pubmed: 37298595
pii: ijms24119644
doi: 10.3390/ijms24119644
pmc: PMC10253536
pii:
doi:

Substances chimiques

Bradykinin S8TIM42R2W
Neurotensin 39379-15-2
AC133 Antigen 0
Peptides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Magdalena Szaryńska (M)

Department of Histology, Faculty of Medicine, Medical University of Gdansk, 80-210 Gdansk, Poland.

Agata Olejniczak-Kęder (A)

Department of Histology, Faculty of Medicine, Medical University of Gdansk, 80-210 Gdansk, Poland.

Kamila Podpłońska (K)

Department of Histology, Faculty of Medicine, Medical University of Gdansk, 80-210 Gdansk, Poland.

Adam Prahl (A)

Department of Organic Chemistry, Faculty of Chemistry, University of Gdansk, 80-308 Gdansk, Poland.

Emilia Iłowska (E)

Department of Organic Chemistry, Faculty of Chemistry, University of Gdansk, 80-308 Gdansk, Poland.

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Classifications MeSH