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  • 11
    In: Molecular Biology of the Cell, American Society for Cell Biology (ASCB), Vol. 17, No. 9 ( 2006-09), p. 4130-4141
    Kurzfassung: We demonstrate that recycling through the endocytic recycling compartment (ERC) is an essential step in FcεRI-induced activation of extracellular signal-regulated kinase (ERK)1/2. We show that ERK1/2 acquires perinuclear localization and colocalizes with Rab 11 and internalized transferrin in FcεRI-activated cells. Moreover, a close correlation exists between the amount of ERC-localized ERK1/2 and the amount of phospho-ERK1/2 that resides in the nucleus. We further show that by activating phosphatidylinositol 4-kinase β (PI4Kβ) and increasing the cellular level of phosphatidylinositol(4) phosphate, neuronal calcium sensor-1 (NCS-1), a calmodulin-related protein, stimulates recycling and thereby enhances FcεRI-triggered activation and nuclear translocation of ERK1/2. Conversely, NCS-1 short hairpin RNA, a kinase dead (KD) mutant of PI4Kβ (KD-PI4Kβ), the pleckstrin homology (PH) domain of FAPP1 as well as RNA interference of synaptotagmin IX or monensin, which inhibit export from the ERC, abrogate FcεRI-induced activation of ERK1/2. Consistently, NCS-1 also enhances, whereas both KD-PI4Kβ and FAPP1-PH domain inhibit, FcεRI-induced release of arachidonic acid/metabolites, a downstream target of ERK1/2 in mast cells. Together, our results demonstrate a novel role for NCS-1 and PI4Kβ in regulating ERK1/2 signaling and inflammatory reactions in mast cells. Our results further identify the ERC as a crucial determinant in controlling ERK1/2 signaling.
    Materialart: Online-Ressource
    ISSN: 1059-1524 , 1939-4586
    Sprache: Englisch
    Verlag: American Society for Cell Biology (ASCB)
    Publikationsdatum: 2006
    ZDB Id: 1474922-1
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 12
    In: The FASEB Journal, Wiley, Vol. 29, No. 8 ( 2015-08), p. 3206-3216
    Materialart: Online-Ressource
    ISSN: 0892-6638 , 1530-6860
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2015
    ZDB Id: 1468876-1
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 13
    Online-Ressource
    Online-Ressource
    American Association for Cancer Research (AACR) ; 2015
    In:  Molecular Cancer Therapeutics Vol. 14, No. 12_Supplement_2 ( 2015-12-01), p. A57-A57
    In: Molecular Cancer Therapeutics, American Association for Cancer Research (AACR), Vol. 14, No. 12_Supplement_2 ( 2015-12-01), p. A57-A57
    Kurzfassung: Background: The EGFR/HER2 signaling network emerges as an effective therapeutic target for Her2 enriched cancers, which is known by its aggressive biological course. Nevertheless, there is evidence that the EGFR/HER2 network may play a key role not only in the HER2-enriched subtype of breast cancer, but also in the similarly aggressive basal-like subtype. We had formerly demonstrated the involvement of miR-125a-3p in the EGFR pathway in prostate cancer. We aimed to study the effect of miR-125a-3p as a potential modulator of the ERBB2/HER2 pathway in basal-like breast cancer subtype. Methods: Using qPCR we calibrated estrogen receptor (ER), ERBB2 (HER2), miR-125a-3p/5p (two isoforms) expression in three cell lines: MDA-MB-231, MCF-7 and SKBR3 (represent the basal-like subtype, ER positive subtype and HER2-enriched subtype respectively). We generated stable MDA-MB-231 cells that overexpress miR-125a-3p and control cells that overexpress scrambled miRNA. In parallel, we established an in vivo platform by injection of miR-125a-3p-overexpressing MDA-MB-231 breast cancer cells to the mammary pad of NUDE mice and evaluated traits of the induced tumors compared with scrambled miRNA-expressing cells (control mice) and response to potential targeted therapy. Results: miR-125a-3p was endogenously expressed in all cell lines, though its expression in MDA-MB-231 cells was significantly lower than in MCF-7 or in SKBR3 cells. Following transfection of cells with miR-125a-3p, MDA-MB-231 cells showed a significant increase in the expression level of ERBB2 mRNA and protein as well as a stronger immunofluorescence staining of ErbB2 than in control cells. Combined treatment of miR-125a-3p-overexpressing cells and trastuzumab induces apoptosis and reduces migration of MDA-MB-231 cells. By tracking Erbb2 internalization and its localization to the lysosoms/the functionality of erbb2 receptor, we determined that trastuzumab caused internalization of ErbB2 and a subsequent lysosomal lysis. In the experimental in vivo platform, starting one week post cells injection/tumor formation?, mice were treated twice a week, for the next 28 days, with 10 mg/Kg trastuzumab or saline as a control. Response to treatment was evaluated by measurement of the tumor size/volume by computerized tomography (CT) or calliper. Both measurements indicated that that the tumors in the miR-125a-3p group that were treated with trastuzumab were significantly smaller than in other groups. Conclusion: our results indicate that miR-125a-3p is capable of inducing a shift in the involvement of key cellular pathway - the ERBB2 pathway that may convert the cell fate and dispose it to anti-HER2 therapies. In an era of personalized medicine, our study proposes a means to enlarge the patient population that may benefit from anti-HER2 therapies. Citation Format: Lihi Ninio-Many, Elad Hikri, Salomon M. Stemmer, Ruth Shalgi, Irit Ben-Aharon. miR-125a-induced cellular switch elicits a response to anti-HER2 targeted therapy in breast cancer cells. [abstract]. In: Proceedings of the AACR-NCI-EORTC International Conference: Molecular Targets and Cancer Therapeutics; 2015 Nov 5-9; Boston, MA. Philadelphia (PA): AACR; Mol Cancer Ther 2015;14(12 Suppl 2):Abstract nr A57.
    Materialart: Online-Ressource
    ISSN: 1535-7163 , 1538-8514
    Sprache: Englisch
    Verlag: American Association for Cancer Research (AACR)
    Publikationsdatum: 2015
    ZDB Id: 2062135-8
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 14
    In: Molecular Cancer Therapeutics, American Association for Cancer Research (AACR), Vol. 20, No. 12_Supplement ( 2021-12-01), p. P064-P064
    Kurzfassung: Fusobacterium nucleatum (FN) is enriched in human colorectal tumors [1] and its presence is correlated with poor prognosis [2] . Bacteriophages ("phages") are naturally occurring, self-amplifying viruses that are highly specific for particular bacterial species and strains and are recognized to have a high intrinsic safety. They offer a promising treatment strategy to both target FN associated with colorectal cancer (CRC) and, by phage engineering, to deliver an anti-tumoral immune-stimulating payload that may enhance the effectivity of other anti-cancer therapies such as checkpoint inhibitors in unresponsive colorectal cancer patients. The major challenge in engineering phages that target FN is the optimization of the eukaryotic payloads for high expression in this bacterial host. Since no data is available about codon usage and non-coding genetic sequences in the genome of FN bacteria, two computational approaches were used to optimize the codon usage for elevated payload expression of the first selected payload, murine IL-15. These approaches involved identifying ribosome binding sites and elongation speeds to optimize codon usage. Following design of an IL-15 expression vector, expression of this eukaryotic payload in FN bacteria was tested in vitro. For phage engineering, a plasmid containing the designed payload sequence was used to introduce the selected IL-15 encoding sequences into the phage genome. FN phage was successfully engineered to deliver a payload encoding the sequence of murine cytokine IL-15. Targeting of FN with engineered phage resulted in IL-15 protein expression in phage-infected bacteria in vitro. Given the specificity of FN for CRC tumors and the ability to locally express a eukaryotic protein by using FN targeting phage to deliver a payload, phage therapy may offer novel treatment approaches for patients with CRC. Citation Format: Lihi Ninio-Many, Yael Zigelman, Nufar Buchshtab, Yifat Elharar, Gal Eylon, Eliya Gidron, Dikla Berko-Ashur, Julian Nicenboim, Lior Zelcbuch, Einav Safyon Gartman, Sharon Kredo-Russo, Noga Kowalsman, Ilya Vainberg Slutskin, Iddo Weiner, Inbar Gahali-Sass, Naomi Zak, Sailaja Puttagunta, Merav Bassan. Novel engineering of therapeutic Fusobacterium nucleatum phage for colorectal cancer treatment [abstract]. In: Proceedings of the AACR-NCI-EORTC Virtual International Conference on Molecular Targets and Cancer Therapeutics; 2021 Oct 7-10. Philadelphia (PA): AACR; Mol Cancer Ther 2021;20(12 Suppl):Abstract nr P064.
    Materialart: Online-Ressource
    ISSN: 1535-7163 , 1538-8514
    Sprache: Englisch
    Verlag: American Association for Cancer Research (AACR)
    Publikationsdatum: 2021
    ZDB Id: 2062135-8
    SSG: 12
    Standort Signatur Einschränkungen Verfügbarkeit
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