Literature DB >> 33406793

Analytical Platforms for the Determination of Phospholipid Turnover in Breast Cancer Tissue: Role of Phospholipase Activity in Breast Cancer Development.

Rosa Perestrelo1, Marijana Petkovic1, Catarina Luís Silva1,2.   

Abstract

Altered lipid metabolism has been associated with tpan class="Chemical">he progression of various cancers, and aberrant expression of enzymes involved in the lipid metabolism has been detected in different stages of cancer. Breast cancer (BC) is one of the cancer types known to be associated with alterations in the lipid metabolism and overexpression of enzymes involved in this metabolism. It has been demonstrated that inhibition of the activity of certain enzymes, such as that of phospholipase A2 in BC cell lines sensitizes these cells and decreases the IC50 values for forthcoming therapy with traditional drugs, such as doxorubicin and tamoxifen. Moreover, other phospholipases, such as phospholipase C and D, are involved in intracellular signal transduction, which emphasizes their importance in cancer development. Finally, BC is assumed to be dependent on the diet and the composition of lipids in nutrients. Despite their importance, analytical approaches that can associate the activity of phospholipases with changes in the lipid composition and distribution in cancer tissues are not yet standardized. In this review, an overview of various analytical platforms that are applied on the study of lipids and phospholipase activity in BC tissues will be given, as well as their association with cancer diagnosis and tumor progression. The methods that are applied to tissues obtained from the BC patients will be emphasized and critically evaluated, regarding their applicability in oncology.

Entities:  

Keywords:  analytical platforms; breast cancer; lipids; statistical analysis

Year:  2021        PMID: 33406793      PMCID: PMC7824782          DOI: 10.3390/metabo11010032

Source DB:  PubMed          Journal:  Metabolites        ISSN: 2218-1989


  106 in total

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Journal:  J Proteomics       Date:  2014-03-29       Impact factor: 4.044

2.  A phosphatidic acid-activated protein kinase and conventional protein kinase C isoforms phosphorylate p22(phox), an NADPH oxidase component.

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Authors:  Christian Vosse; Carina Wienken; Cristina Cadenas; Heiko Hayen
Journal:  J Chromatogr A       Date:  2018-06-30       Impact factor: 4.759

4.  Comparison of different procedures for the lipid extraction from HL-60 cells: a MALDI-TOF mass spectrometric study.

Authors:  Marijana Petković; Andreas Vocks; Matthias Müller; Jürgen Schiller; Jürgen Arnhold
Journal:  Z Naturforsch C J Biosci       Date:  2005 Jan-Feb

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Authors:  Eva Cífková; Michal Holčapek; Miroslav Lísa; David Vrána; Jiří Gatěk; Bohuslav Melichar
Journal:  Anal Bioanal Chem       Date:  2014-10-29       Impact factor: 4.142

6.  Lipidomic analysis of phospholipids from human mammary epithelial and breast cancer cell lines.

Authors:  M Luísa Dória; Cândida Z Cotrim; Cláudia Simões; Bárbara Macedo; Pedro Domingues; M Rosário Domingues; Luisa A Helguero
Journal:  J Cell Physiol       Date:  2013-02       Impact factor: 6.384

Review 7.  Protein kinase C isoforms: Multi-functional regulators of cell life and death.

Authors:  Mary E Reyland
Journal:  Front Biosci (Landmark Ed)       Date:  2009-01-01

8.  Peroxisome proliferator-activated receptor-gamma protects ERBB2-positive breast cancer cells from palmitate toxicity.

Authors:  Antonis Kourtidis; Rekha Srinivasaiah; Richard D Carkner; M Julia Brosnan; Douglas S Conklin
Journal:  Breast Cancer Res       Date:  2009-03-19       Impact factor: 6.466

9.  Overexpression of group II phospholipase A2 in human breast cancer tissues is closely associated with their malignant potency.

Authors:  S Yamashita; J Yamashita; M Ogawa
Journal:  Br J Cancer       Date:  1994-06       Impact factor: 7.640

10.  Lipidomic study of cell lines reveals differences between breast cancer subtypes.

Authors:  Finnur Freyr Eiriksson; Martha Kampp Nøhr; Margarida Costa; Sigridur Klara Bödvarsdottir; Helga Margret Ögmundsdottir; Margret Thorsteinsdottir
Journal:  PLoS One       Date:  2020-04-14       Impact factor: 3.240

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