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Title:Molecular heterogeneity in breast carcinoma cells with increased invasive capacities
Authors:ID Negro, Giulia (Author)
ID Aschenbrenner, Bertram (Author)
ID Kranjc Brezar, Simona (Author)
ID Čemažar, Maja (Author)
ID Cör, Andrej (Author)
ID Gašljević, Gorana (Author)
ID Sorokin, Maxim (Author)
ID Buzdin, Anton A. (Author)
ID Callari, Maurizio (Author)
ID Kvitsaridze, Irma (Author)
Files:.pdf PDF - Presentation file, download (2,52 MB)
MD5: 91D15B8F3DA5062CF57EFA37E6E90270
 
Language:English
Typology:1.01 - Original Scientific Article
Organization:Logo OI - Institute of Oncology
Abstract:Metastatic progression of breast cancer is still a challenge in clinical oncology. Therefore, an elucidation how carcinoma cells belonging to different breast cancer subtypes realize their metastatic capacities is needed. The aim of this study was to elucidate a similarity of activated molecular pathways underlying an enhancement of invasiveness of carcinoma cells belonging to different breast carcinoma subtypes. Materials and methods. In order to reach this aim, parental and invasive (INV) MDA-MB-231 (triple-negative), T47D (hormone receptor-positive), and Au565 (Her2-positive) breast carcinoma cells were used and their molecular phenotypes were compared using a proteomic approach. Results. Independently from breast cancer subtypes, INV cells have demonstrated fibroblast-like morphology accompanied by enhancement of invasive and migratory capacities, increased expression of cancer stem cell markers, and delayed tumor growth in in vivo animal models. However, the global proteomic analysis has highlighted that INV cells were different in protein expressions from the parental cells, and Her2-positive Au565-INV cells showed the most pronounced molecular differences compared to the triple-negative MDA-MB-231-INV and hormone receptor-positive T47D-INV cells. Although Au565-INV breast carcinoma cells possessed the highest number of deregulated proteins, they had the lowest overlapping in proteins commonly expressed in MDA-MB-231-INV and T47D-INV cells. Conclusions. We can conclude that hormone receptor-positive cells with increased invasiveness acquire the molecular characteristics of triple-negative breast cancer cells, whereas Her2-positive INV cells specifically changed their own molecular phenotype with very limited partaking in the involved pathways found in the MDA-MB-231-INV and T47D-INV cells. Since hormone receptor-positive invasive cells share their molecular properties with triple-negative breast cancer cells, we assume that these types of metastatic disease can be treated rather equally with an option to add anti-hormonal agents. In contrast, Her2-positive metastasis should be carefully evaluated for more effective therapeutic approaches which are distinct from the triple-negative and hormone-positive metastatic breast cancers.
Keywords:breast cancer, cancer stem cells, invasiveness, migration, metastasis
Publication status:Published
Publication version:Version of Record
Publication date:01.01.2020
Publisher:Association of Radiology and Oncology
Year of publishing:2020
Number of pages:str. 103-118, XI
Numbering:Vol. 54, no. 1
Source:Ljubljana
PID:20.500.12556/DiRROS-19234 New window
UDC:616-07
ISSN on article:1318-2099
DOI:10.2478/raon-2020-0007 New window
COBISS.SI-ID:3514235 New window
Copyright:by Authors
Publication date in DiRROS:11.07.2024
Views:428
Downloads:182
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Record is a part of a journal

Title:Radiology and oncology
Shortened title:Radiol. oncol.
Publisher:Slovenian Medical Society - Section of Radiology, Croatian Medical Association - Croatian Society of Radiology
ISSN:1318-2099
COBISS.SI-ID:32649472 New window

Secondary language

Language:Slovenian
Keywords:rak dojke, rakave celice, invazivnost, potovanje, metastaze


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