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  1. Article ; Online: Modulation of Akt vs Stat3 activity by the focal adhesion kinase in non-neoplastic mouse fibroblasts.

    Geletu, Mulu / Adan, Hanad / Niit, Maximillian / Arulanandam, Rozanne / Carefoot, Esther / Hoskin, Victoria / Sina, Diana / Elliott, Bruce / Gunning, Patrick / Raptis, Leda

    Experimental cell research

    2021  Volume 411, Issue 1, Page(s) 112731

    Abstract: Adhesion of cells to each other and to the extracellular matrix (ECM) are both required for cellular functions. Cell-to-cell adhesion is mediated by cadherins, and their engagement triggers the activation of Stat3, which offers a potent survival signal. ... ...

    Abstract Adhesion of cells to each other and to the extracellular matrix (ECM) are both required for cellular functions. Cell-to-cell adhesion is mediated by cadherins, and their engagement triggers the activation of Stat3, which offers a potent survival signal. Adhesion to the ECM on the other hand, activates FAK which attracts and activates Src, as well as receptor tyrosine kinases (RTKs), the PI3k/Akt and Ras/Erk pathways. However, the effect of cell density upon FAK and Akt activity has not been examined. We now demonstrate that, interestingly, despite being potent Stat3 activators, Src and RTKs are unable to activate Stat3 in sparsely growing (i.e., without cadherin engagement), non-neoplastic cells attached to the ECM. In contrast, cell aggregation (i.e., cadherin engagement in the absence of adhesion to a solid substratum) was found to activate both Stat3 and Akt. Pharmacologic or genetic reduction of FAK activity abolished Akt activity at low densities, indicating that FAK is an important activator of Akt in this setting. Notably, FAK knockout increased cellular sensitivity to the Stat3 inhibitor CPA7, while FAK reintroduction restored resistance to this drug. These findings suggest a complementary role of integrin/FAK/Akt and cadherin/Stat3-mediated pro-survival pathways, which may be of significance during neoplastic transformation and metastasis.
    Language English
    Publishing date 2021-07-14
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 1493-x
    ISSN 1090-2422 ; 0014-4827
    ISSN (online) 1090-2422
    ISSN 0014-4827
    DOI 10.1016/j.yexcr.2021.112731
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Erratum to "Modulation of Akt vs Stat3 activity by the focal adhesion kinase in non-neoplastic mouse fibroblasts" [Exp. Cell Res. 404 (1) (2021) 112601].

    Geletu, Mulu / Adan, Hanad / Niit, Maximillian / Arulanandam, Rozanne / Carefoot, Esther / Hoskin, Victoria / Sina, Diana / Elliott, Bruce / Gunning, Patrick / Raptis, Leda

    Experimental cell research

    2021  Volume 411, Issue 1, Page(s) 112732

    Language English
    Publishing date 2021-07-30
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 1493-x
    ISSN 1090-2422 ; 0014-4827
    ISSN (online) 1090-2422
    ISSN 0014-4827
    DOI 10.1016/j.yexcr.2021.112732
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Modulation of Akt vs Stat3 activity by the focal adhesion kinase in non-neoplastic mouse fibroblasts.

    Geletu, Mulu / Adan, Hanad / Niit, Maximillian / Arulanandam, Rozanne / Carefoot, Esther / Hoskin, Victoria / Sina, Diana / Elliott, Bruce / Gunning, Patrick / Raptis, Leda

    Experimental cell research

    2021  Volume 404, Issue 1, Page(s) 112601

    Abstract: Adhesion of cells to each other and to the extracellular matrix (ECM) are both required for cellular functions. Cell-to-cell adhesion is mediated by cadherins and their engagement triggers the activation of Stat3, which offers a potent survival signal. ... ...

    Abstract Adhesion of cells to each other and to the extracellular matrix (ECM) are both required for cellular functions. Cell-to-cell adhesion is mediated by cadherins and their engagement triggers the activation of Stat3, which offers a potent survival signal. Adhesion to the ECM on the other hand, activates FAK which attracts and activates Src, as well as receptor tyrosine kinases (RTKs), the PI3k/Akt and Ras/Erk pathways. However, the effect of cell density upon FAK and Akt activity has not been examined. We now demonstrate that, interestingly, despite being potent Stat3 activators, Src and RTKs are unable to activate Stat3 in sparsely growing (i.e., without cadherin engagement), non-neoplastic cells attached to the ECM. In contrast, cell aggregation (i.e., cadherin engagement in the absence of adhesion to a solid substratum) was found to activate both Stat3 and Akt. Pharmacologic or genetic reduction of FAK activity abolished Akt activity at low densities, indicating that FAK is an important activator of Akt in this setting. Notably, FAK knockout increased cellular sensitivity to the Stat3 inhibitor CPA7, while FAK reintroduction restored resistance to this drug. These findings suggest a complementary role of integrin/FAK/Akt and cadherin/Stat3-mediated pro-survival pathways, which may be of significance during neoplastic transformation and metastasis.
    MeSH term(s) Animals ; Cadherins/metabolism ; Cell Adhesion/physiology ; Cell Survival/physiology ; Cell Transformation, Neoplastic/metabolism ; Extracellular Matrix/metabolism ; Fibroblasts/metabolism ; Focal Adhesion Protein-Tyrosine Kinases/metabolism ; Humans ; Mice ; Phosphatidylinositol 3-Kinases/metabolism ; Proto-Oncogene Proteins c-akt/metabolism ; STAT3 Transcription Factor/metabolism ; Signal Transduction/physiology
    Chemical Substances Cadherins ; STAT3 Transcription Factor ; STAT3 protein, human ; Focal Adhesion Protein-Tyrosine Kinases (EC 2.7.10.2) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2021-05-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1493-x
    ISSN 1090-2422 ; 0014-4827
    ISSN (online) 1090-2422
    ISSN 0014-4827
    DOI 10.1016/j.yexcr.2021.112601
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Regulation of Differentiation of HC11 Mouse Breast Epithelial Cells by the Signal Transducer and Activator of Transcription-3.

    Niit, Maximillian / Geletu, Mulu / Taha, Zaid / Arulanandam, Rozanne / Cass, Jamaica / Hoskin, Victoria / Elliott, Bruce / Gunning, Patrick / Raptis, Leda

    Anticancer research

    2019  Volume 39, Issue 6, Page(s) 2749–2756

    Abstract: Background/aim: The differentiation of the mouse breast epithelial cell line HC11 is known to require confluence as well as the addition of hydrocortisone, insulin and prolactin.: Materials and methods: Since confluence, which triggers the engagement ...

    Abstract Background/aim: The differentiation of the mouse breast epithelial cell line HC11 is known to require confluence as well as the addition of hydrocortisone, insulin and prolactin.
    Materials and methods: Since confluence, which triggers the engagement of the cell-to-cell adhesion molecule E-cadherin, induces a dramatic increase in the activity of signal transducer and activator of transcription-3 (Stat3), we examined the role of Stat3 in HC11 cell differentiation.
    Results: Stat3 inhibition abolished differentiation, indicating that Stat3 activity is critically required. However, expression of the mutationally activated form of Stat3 (Stat3C), rather than promoting, it was found to block cell differentiation, even when expressed in low levels, and in the absence of full neoplastic conversion.
    Conclusion: The strength of the E-cadherin/Stat3 signal is key for the outcome of the differentiation process.
    MeSH term(s) Animals ; Cadherins/metabolism ; Cell Differentiation ; Epithelial Cells/cytology ; Female ; Mammary Glands, Animal/cytology ; Mammary Glands, Animal/metabolism ; Mice ; Mutation ; Phosphorylation ; STAT3 Transcription Factor/genetics ; STAT3 Transcription Factor/metabolism ; Signal Transduction ; Tyrosine/metabolism
    Chemical Substances Cadherins ; Cdh1 protein, mouse ; STAT3 Transcription Factor ; Stat3 protein, mouse ; Tyrosine (42HK56048U)
    Language English
    Publishing date 2019-06-05
    Publishing country Greece
    Document type Journal Article
    ZDB-ID 604549-2
    ISSN 1791-7530 ; 0250-7005
    ISSN (online) 1791-7530
    ISSN 0250-7005
    DOI 10.21873/anticanres.13401
    Database MEDical Literature Analysis and Retrieval System OnLINE

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