Your browser doesn't support javascript.
loading
Novel Thieno [2,3-b]pyridine Anticancer Compound Lowers Cancer Stem Cell Fraction Inducing Shift of Lipid to Glucose Metabolism.
Pervan, Matij; Marijan, Sandra; Markotic, Anita; Pilkington, Lisa I; Haverkate, Natalie A; Barker, David; Reynisson, Jóhannes; Meic, Luka; Radan, Mila; Cikes Culic, Vedrana.
Afiliação
  • Pervan M; Department of Medical Chemistry and Biochemistry, University of Split School of Medicine, 21000 Split, Croatia.
  • Marijan S; Department of Medical Chemistry and Biochemistry, University of Split School of Medicine, 21000 Split, Croatia.
  • Markotic A; Department of Medical Chemistry and Biochemistry, University of Split School of Medicine, 21000 Split, Croatia.
  • Pilkington LI; School of Chemical Sciences, The University of Auckland, Auckland 1010, New Zealand.
  • Haverkate NA; School of Chemical Sciences, The University of Auckland, Auckland 1010, New Zealand.
  • Barker D; School of Chemical Sciences, The University of Auckland, Auckland 1010, New Zealand.
  • Reynisson J; MacDiarmid Institute for Advanced Materials and Nanotechnology, Wellington 6140, New Zealand.
  • Meic L; School of Pharmacy and Bioengineering, Keele University, Staffordshire ST5 5BG, UK.
  • Radan M; Department of Biochemistry, Faculty of Chemistry and Technology, University of Split, 21000 Split, Croatia.
  • Cikes Culic V; Department of Biochemistry, Faculty of Chemistry and Technology, University of Split, 21000 Split, Croatia.
Int J Mol Sci ; 23(19)2022 Sep 28.
Article em En | MEDLINE | ID: mdl-36232754
Due to the role of cancer stem cells (CSCs) in tumor resistance and glycosphingolipid (GSL) involvement in tumor pathogenesis, we investigated the effect of a newly synthesized compound (3-amino-N-(3-chloro-2-methylphenyl)-5-oxo-5,6,7,8-tetrahydrothieno[2,3-b]quinoline-2-carboxamide 1 on the percentage of CSCs and the expression of six GSLs on CSCs and non-CSCs on breast cancer cell lines (MDA-MB-231 and MCF-7). We also investigated the effect of 1 on the metabolic profile of these cell lines. The MTT assay was used for cytotoxicity determination. Apoptosis and expression of GSLs were assessed by flow cytometry. A GC-MS-coupled system was used for the separation and identification of metabolites. Compound 1 was cytotoxic for both cell lines, and the majority of cells died by treatment-induced apoptosis. The percentage of CSCs was significantly lower in the MDA-MB-231 cell line. Treatment with 1 caused a decrease of CSC IV6Neu5Ac-nLc4Cer+ MDA-MB-231 cells. In the MCF-7 cell line, the percentage of GalNAc-GM1b+ CSCs was increased, while the expression of Gg3Cer was decreased in both CSC and non-CSC. Twenty-one metabolites were identified by metabolic profiling. The major impact of the treatment was in glycolysis/gluconeogenesis, pyruvate and inositol metabolism. Compound 1 exhibited higher potency in MBA-MB-231 cells, and it deserves further examination.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Neoplasias da Mama / Antineoplásicos Limite: Female / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Croácia País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Quinolinas / Neoplasias da Mama / Antineoplásicos Limite: Female / Humans Idioma: En Revista: Int J Mol Sci Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Croácia País de publicação: Suíça