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  1. Article ; Online: Glycosylation Modulates Plasma Membrane Trafficking of CD24 in Breast Cancer Cells.

    Chantziou, Amanda / Theodorakis, Kostas / Polioudaki, Hara / de Bree, Eelco / Kampa, Marilena / Mavroudis, Dimitris / Castanas, Elias / Theodoropoulos, Panayiotis A

    International journal of molecular sciences

    2021  Volume 22, Issue 15

    Abstract: In breast cancer, expression of Cluster of Differentiation 24 (CD24), a small GPI-anchored glycoprotein at the cell periphery, is associated with metastasis and immune escape, while its absence is associated with tumor-initiating capacity. Since the ... ...

    Abstract In breast cancer, expression of Cluster of Differentiation 24 (CD24), a small GPI-anchored glycoprotein at the cell periphery, is associated with metastasis and immune escape, while its absence is associated with tumor-initiating capacity. Since the mechanism of CD24 sorting is unknown, we investigated the role of glycosylation in the subcellular localization of CD24. Expression and localization of wild type N36- and/or N52-mutated CD24 were analyzed using immunofluorescence in luminal (MCF-7) and basal B (MDA-MB-231 and Hs578T) breast cancer cells lines, as well as HEK293T cells. Endogenous and exogenously expressed wild type and mutated CD24 were found localized at the plasma membrane and the cytoplasm, but not the nucleoplasm. The cell lines showed different kinetics for the sorting of CD24 through the secretory/endocytic pathway. N-glycosylation, especially at N52, and its processing in the Golgi were critical for the sorting and expression of CD24 at the plasma membrane of HEK293T and basal B type cells, but not of MCF-7 cells. In conclusion, our study highlights the contribution of N-glycosylation for the subcellular localization of CD24. Aberrant N-glycosylation at N52 of CD24 could account for the lack of CD24 expression at the cell surface of basal B breast cancer cells.
    MeSH term(s) Breast Neoplasms/metabolism ; CD24 Antigen/metabolism ; Cell Line, Tumor ; Cell Membrane/metabolism ; Female ; Glycosylation ; Humans
    Chemical Substances CD24 Antigen ; CD24 protein, human
    Language English
    Publishing date 2021-07-29
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms22158165
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Corrigendum to "The sequence [EKRKI(E/R)(K/L/R/S/T)] is a nuclear localization signal for importin 7 binding (NLS7)" [Biochim Biophys Acta Gen Subj. 2021 May; 1865(5): 129851].

    Panagiotopoulos, Athanasios A / Polioudaki, Chara / Ntallis, Sotirios G / Dellis, Dimitris / Notas, George / Panagiotidis, Christos A / Theodoropoulos, Panayiotis A / Castanas, Elias / Kampa, Marilena

    Biochimica et biophysica acta. General subjects

    2021  Volume 1865, Issue 7, Page(s) 129887

    Language English
    Publishing date 2021-03-10
    Publishing country Netherlands
    Document type Published Erratum
    ZDB-ID 60-7
    ISSN 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbagen.2021.129887
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: The sequence [EKRKI(E/R)(K/L/R/S/T)] is a nuclear localization signal for importin 7 binding (NLS7).

    Panagiotopoulos, Athanasios A / Polioudaki, Chara / Ntallis, Sotirios G / Dellis, Dimitris / Notas, George / Panagiotidis, Christos A / Theodoropoulos, Panayiotis A / Castanas, Elias / Kampa, Marilena

    Biochimica et biophysica acta. General subjects

    2021  Volume 1865, Issue 5, Page(s) 129851

    Abstract: Background: Nuclear translocation of large proteins is mediated through specific protein carriers, collectively named karyopherins (importins, exportins and adaptor proteins). Cargo proteins are recognized by importins through specific motifs, known as ... ...

    Abstract Background: Nuclear translocation of large proteins is mediated through specific protein carriers, collectively named karyopherins (importins, exportins and adaptor proteins). Cargo proteins are recognized by importins through specific motifs, known as nuclear localization signals (NLS). However, only the NLS recognized by importin α and transportin (M9 NLS) have been identified so far METHODS: An unsupervised in silico approach was used, followed by experimental validation.
    Results: We identified the sequence EKRKI(E/R)(K/L/R/S/T) as an NLS signal for importin 7 recognition. This sequence was validated in the breast cancer cell line T47D, which expresses importin 7. Finally, we verified that importin 7-mediated nuclear protein transport is affected by cargo protein phosphorylation.
    Conclusions: The NLS sequence for importin 7 was identified and we propose this approach as an identification method of novel specific NLS sequences for β-karyopherin family members.
    General significance: Elucidating the complex relationships of the nuclear transporters and their cargo proteins may help in laying the foundation for the development of novel therapeutics, targeting specific importins, with an immediate translational impact.
    MeSH term(s) Active Transport, Cell Nucleus ; Amino Acid Sequence ; Breast Neoplasms/metabolism ; Cell Line, Tumor ; Female ; Humans ; Karyopherins/chemistry ; Karyopherins/metabolism ; Models, Molecular ; Nuclear Localization Signals ; Phosphorylation ; Receptors, Cytoplasmic and Nuclear/chemistry ; Receptors, Cytoplasmic and Nuclear/metabolism
    Chemical Substances IPO7 protein, human ; Karyopherins ; Nuclear Localization Signals ; Receptors, Cytoplasmic and Nuclear
    Language English
    Publishing date 2021-01-19
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 60-7
    ISSN 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1872-8006 ; 1879-2596 ; 1879-260X ; 1879-2642 ; 1879-2618 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbagen.2021.129851
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: The sequence [EKRKI(E/R)(K/L/R/S/T)] is a nuclear localization signal for importin 7 binding (NLS7)

    Panagiotopoulos, Athanasios A / Polioudaki, Chara / Ntallis, Sotirios G / Dellis, Dimitris / Notas, George / Panagiotidis, Christos A / Theodoropoulos, Panayiotis A / Castanas, Elias / Kampa, Marilena

    Biochimica et biophysica acta. 2021 May, v. 1865, no. 5

    2021  

    Abstract: Nuclear translocation of large proteins is mediated through specific protein carriers, collectively named karyopherins (importins, exportins and adaptor proteins). Cargo proteins are recognized by importins through specific motifs, known as nuclear ... ...

    Abstract Nuclear translocation of large proteins is mediated through specific protein carriers, collectively named karyopherins (importins, exportins and adaptor proteins). Cargo proteins are recognized by importins through specific motifs, known as nuclear localization signals (NLS). However, only the NLS recognized by importin α and transportin (M9 NLS) have been identified so farAn unsupervised in silico approach was used, followed by experimental validation.We identified the sequence EKRKI(E/R)(K/L/R/S/T) as an NLS signal for importin 7 recognition. This sequence was validated in the breast cancer cell line T47D, which expresses importin 7. Finally, we verified that importin 7-mediated nuclear protein transport is affected by cargo protein phosphorylation.The NLS sequence for importin 7 was identified and we propose this approach as an identification method of novel specific NLS sequences for β-karyopherin family members.Elucidating the complex relationships of the nuclear transporters and their cargo proteins may help in laying the foundation for the development of novel therapeutics, targeting specific importins, with an immediate translational impact.
    Keywords breast neoplasms ; cell lines ; computer simulation ; importins ; neoplasm cells ; nuclear localization signals ; therapeutics ; transporters
    Language English
    Dates of publication 2021-05
    Publishing place Elsevier B.V.
    Document type Article
    Note NAL-light
    ZDB-ID 840755-1
    ISSN 0304-4165
    ISSN 0304-4165
    DOI 10.1016/j.bbagen.2021.129851
    Database NAL-Catalogue (AGRICOLA)

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  5. Article: Stem cell technology in breast cancer: current status and potential applications.

    Chiotaki, Rena / Polioudaki, Hara / Theodoropoulos, Panayiotis A

    Stem cells and cloning : advances and applications

    2016  Volume 9, Page(s) 17–29

    Abstract: Breast cancer, the leading cause of cancer among females, is supported by the presence of a rare subset of undifferentiated cells within the tumor, identified as breast cancer stem cells (BCSCs). BCSCs underlie the mechanisms of tumor initiation and ... ...

    Abstract Breast cancer, the leading cause of cancer among females, is supported by the presence of a rare subset of undifferentiated cells within the tumor, identified as breast cancer stem cells (BCSCs). BCSCs underlie the mechanisms of tumor initiation and sustenance and are implicated in the dissemination of the primary tumor to metastatic sites, as they have been found circulating in the blood of breast cancer patients. The discovery of BCSCs has generated a great amount of interest among the scientific community toward their isolation, molecular characterization, and therapeutic targeting. In this review, after summarizing the literature on molecular characterization of BCSCs and methodologies used for their isolation, we will focus on recent data supporting their molecular and functional heterogeneity. Additionally, following a synopsis of the latest approaches for BCSC targeting, we will specifically emphasize on the therapeutic use of naïve or engineered normal stem cells in the treatment of breast cancer and present contradictory findings challenging their safety.
    Language English
    Publishing date 2016-04-26
    Publishing country New Zealand
    Document type Journal Article ; Review
    ISSN 1178-6957
    ISSN 1178-6957
    DOI 10.2147/SCCAA.S72836
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Corrigendum to "Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental in vitro validation" [Comput Struct Biotechnol J 20 (2022) 5952-5961].

    Panagiotopoulos, Athanasios A / Kalyvianaki, Konstantina / Tsodoulou, Paraskevi K / Darivianaki, Maria N / Dellis, Dimitris / Notas, George / Daskalakis, Vangelis / Theodoropoulos, Panayiotis A / Panagiotidis, Christos A / Castanas, Elias / Kampa, Marilena

    Computational and structural biotechnology journal

    2022  Volume 22, Page(s) 1

    Abstract: This corrects the article DOI: 10.1016/j.csbj.2022.10.015.]. ...

    Abstract [This corrects the article DOI: 10.1016/j.csbj.2022.10.015.].
    Language English
    Publishing date 2022-12-30
    Publishing country Netherlands
    Document type Published Erratum
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2022.12.038
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Cancer stem cells in solid and liquid tissues of breast cancer patients: characterization and therapeutic perspectives.

    Chiotaki, Rena / Polioudaki, Hara / Theodoropoulos, Panayiotis A

    Current cancer drug targets

    2015  Volume 15, Issue 3, Page(s) 256–269

    Abstract: Breast cancer stem cells (BCSCs) represent a heterogeneous subpopulation of rare cells within breast cancer tumors, displaying an enhanced tumor initiating capability and underlying disease progression and therapy resistance. Unraveling their phenotypic, ...

    Abstract Breast cancer stem cells (BCSCs) represent a heterogeneous subpopulation of rare cells within breast cancer tumors, displaying an enhanced tumor initiating capability and underlying disease progression and therapy resistance. Unraveling their phenotypic, biological and functional profile is a major challenge in the context of diminishing patient mortality. In this review, following a brief description on how cancer stem cells (CSCs) and their microenvironment contribute to tumor preservation and heterogeneity, we summarize the current literature regarding the molecular signature of BCSCs either localized in the primary tumor or circulating in the blood of breast cancer patients. We present recent data on specific stem and epithelial-to-mesenchymal transition (EMT) markers designating the BCSC subpopulation and underline their pathogenic significance. The molecular characterization of BCSCs has promoted the design of novel therapeutic approaches targeting the BCSC subpopulation which are currently being experimentally and clinically evaluated. We highlight recent advances on the development of novel BCSC-targeting therapeutic strategies including the inhibition of cell signaling pathways, differentiation therapy, metabolic interference and nucleotide-, bio- and nano-technology based approaches. Eliminating the chemo- and radio-resistance properties of breast cancer tumor cells via BCSC-directed therapies, combined to conventional therapeutic approaches, will augment the effectiveness of breast cancer treatment and improve the clinical outcome of breast cancer patients.
    MeSH term(s) Antineoplastic Agents/pharmacology ; Breast Neoplasms/drug therapy ; Breast Neoplasms/metabolism ; Breast Neoplasms/pathology ; Epithelial-Mesenchymal Transition ; Female ; Humans ; Neoplastic Cells, Circulating ; Neoplastic Stem Cells/drug effects ; Neoplastic Stem Cells/metabolism ; Neoplastic Stem Cells/pathology ; Tumor Microenvironment
    Chemical Substances Antineoplastic Agents
    Language English
    Publishing date 2015-02-09
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 2064824-8
    ISSN 1873-5576 ; 1568-0096
    ISSN (online) 1873-5576
    ISSN 1568-0096
    DOI 10.2174/1568009615666150211102503
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article: Recognition motifs for importin 4 [(L)PPRS(G/P)P] and importin 5 [KP(K/Y)LV] binding, identified by bio-informatic simulation and experimental

    Panagiotopoulos, Athanasios A / Kalyvianaki, Konstantina / Tsodoulou, Paraskevi K / Darivianaki, Maria N / Dellis, Dimitris / Notas, George / Daskalakis, Vangelis / Theodoropoulos, Panayiotis A / Panagiotidis, Christos Α / Castanas, Elias / Kampa, Marilena

    Computational and structural biotechnology journal

    2022  Volume 20, Page(s) 5952–5961

    Abstract: Nuclear translocation of large proteins is mediated through karyopherins, carrier proteins recognizing specific motifs of cargo proteins, known as nuclear localization signals (NLS). However, only few NLS signals have been reported until now. In the ... ...

    Abstract Nuclear translocation of large proteins is mediated through karyopherins, carrier proteins recognizing specific motifs of cargo proteins, known as nuclear localization signals (NLS). However, only few NLS signals have been reported until now. In the present work, NLS signals for Importins 4 and 5 were identified through an unsupervised
    Language English
    Publishing date 2022-10-26
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 2694435-2
    ISSN 2001-0370
    ISSN 2001-0370
    DOI 10.1016/j.csbj.2022.10.015
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Epithelial/Mesenchymal Characteristics and PD-L1 Co-Expression in CTCs of Metastatic Breast Cancer Patients Treated with Eribulin: Correlation with Clinical Outcome.

    Polioudaki, Hara / Mala, Anastasia / Gkimprixi, Eleni / Papadaki, Maria A / Chantziou, Amanda / Tzardi, Maria / Mavroudis, Dimitris / Agelaki, Sofia / Theodoropoulos, Panayiotis A

    Cancers

    2020  Volume 12, Issue 12

    Abstract: We aimed to evaluate the co-expression of PD-L1 and epithelial-mesenchymal markers in CTCs from metastatic breast cancer (MBC) patients and to determine if there is any relationship with patients' outcome after eribulin treatment. Using cytospin ... ...

    Abstract We aimed to evaluate the co-expression of PD-L1 and epithelial-mesenchymal markers in CTCs from metastatic breast cancer (MBC) patients and to determine if there is any relationship with patients' outcome after eribulin treatment. Using cytospin preparations of peripheral blood mononuclear cells (PBMCs) from MBC patients treated with eribulin and a combination of immunocytochemistry and immunofluorescence, we quantified PD-L1, keratins and vimentin in single and cluster CTCs on days 1 and 8 of the first-treatment cycle. CTCs (
    Language English
    Publishing date 2020-12-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2527080-1
    ISSN 2072-6694
    ISSN 2072-6694
    DOI 10.3390/cancers12123735
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  10. Article ; Online: A simple open source bioinformatic methodology for initial exploration of GPCR ligands' agonistic/antagonistic properties.

    Panagiotopoulos, Athanasios A / Papachristofi, Christina / Kalyvianaki, Konstantina / Malamos, Panagiotis / Theodoropoulos, Panayiotis A / Notas, George / Calogeropoulou, Theodora / Castanas, Elias / Kampa, Marilena

    Pharmacology research & perspectives

    2020  Volume 8, Issue 4, Page(s) e00600

    Abstract: Drug development is an arduous procedure, necessitating testing the interaction of a large number of potential candidates with potential interacting (macro)molecules. Therefore, any method which could provide an initial screening of potential candidate ... ...

    Abstract Drug development is an arduous procedure, necessitating testing the interaction of a large number of potential candidates with potential interacting (macro)molecules. Therefore, any method which could provide an initial screening of potential candidate drugs might be of interest for the acceleration of the procedure, by highlighting interesting compounds, prior to in vitro and in vivo validation. In this line, we present a method which may identify potential hits, with agonistic and/or antagonistic properties on GPCR receptors, integrating the knowledge on signaling events triggered by receptor activation (GPCRs binding to G
    MeSH term(s) Computational Biology/methods ; Crystallography ; Drug Development/methods ; Guanosine Diphosphate/metabolism ; Guanosine Triphosphate/metabolism ; Humans ; Ligands ; Molecular Docking Simulation ; Receptors, G-Protein-Coupled/agonists ; Receptors, G-Protein-Coupled/antagonists & inhibitors ; Receptors, G-Protein-Coupled/metabolism ; Signal Transduction
    Chemical Substances Ligands ; Receptors, G-Protein-Coupled ; Guanosine Diphosphate (146-91-8) ; Guanosine Triphosphate (86-01-1)
    Language English
    Publishing date 2020-07-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2740389-0
    ISSN 2052-1707 ; 2052-1707
    ISSN (online) 2052-1707
    ISSN 2052-1707
    DOI 10.1002/prp2.600
    Database MEDical Literature Analysis and Retrieval System OnLINE

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