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Showing 1 to 11 of 11 for “"Antibody-drug conjugate (ADC)"”.

  1. Synthesis and biological evaluation of auristatin-F recombinant antibody-drug conjugates for cancer therapy

    … as a contribution to the emerging field of antibody-drug conjugate (ADC) therapeutics, in which novel ADCs were generated and biologically evaluated for therapeutic potential and specificity towards cancer cells. SNAP-tag site-directed conjugation was employed in order to overcome the …

    cape-town Repository record for Synthesis and biological evaluation of auristatin-F recombinant antibody-drug conjugates for cancer therapy (opens in a new tab)

  2. Targeting the actin cytoskeleton in HER2+ metastatic cancer cells using a macrolide toxin

    … B (MycB), as a potential warhead for a novel antibody drug conjugate (ADC) to target highly metastatic HER2+ breast and ovarian cancers. We found that MycB treatment of HER2+ breast (SKBR3, MDA-MB-453) and ovarian (SKOV3) cancer cells led to loss of viability (IC50 values ≤ 64 nM). Sub-lethal …

    queens Repository record for Targeting the actin cytoskeleton in HER2+ metastatic cancer cells using a macrolide toxin (opens in a new tab)

  3. A NOVEL, RAS-INDEPENDENT ROLE FOR NF1 IN MICROTUBULE DYNAMICS AND DAMAGE REPAIR DICTATES SENSITIVITY TO T-DM1 IN HER2 POSITIVE BREAST CANCER.

    … cancer cells to T-DM1, the first approved Antibody-drug conjugate (ADC) in breast cancer, through a novel, RAS-independent function on microtubular dynamics and repair. NF1 exhibits all biochemical properties of a bona fide MAP and specifically enhances intratubular repair. These results …

    milano Repository record for A NOVEL, RAS-INDEPENDENT ROLE FOR NF1 IN MICROTUBULE DYNAMICS AND DAMAGE REPAIR DICTATES SENSITIVITY TO T-DM1 IN HER2 POSITIVE BREAST CANCER. (opens in a new tab)

  4. The Mechanism of cGAMP Induced Antitumor Effect and Its Application in Treating Cancer and Antibody Generation

    … toxicity. Chapter Four describes developing an antibody-drug conjugate (ADC) that links a STING agonist to antibodies targeting EGFR, prevalent in many cancers. This STING ADC activates various immune cells and promotes macrophage polarization within tumors. Chapter Five utilizes cGAMP as an …

    utswmed Repository record for The Mechanism of cGAMP Induced Antitumor Effect and Its Application in Treating Cancer and Antibody Generation (opens in a new tab)

  5. NF1 AS A REGULATOR OF CYTOSKELETON DYNAMICS AND BIOMARKER FOR DECISION-MAKING IN HER2-POSITIVE BREAST CANCER

    … cells demonstrated exquisite sensitivity to the antibody-drug conjugate (ADC) trastuzumab emtansine (T-DM1). This hypersensitivity was specific to the mertansine MT-targeting component (DM1) since it was i) replicated by the naked payload but not the antibody alone; ii) absent with other ADCs …

    milano Repository record for NF1 AS A REGULATOR OF CYTOSKELETON DYNAMICS AND BIOMARKER FOR DECISION-MAKING IN HER2-POSITIVE BREAST CANCER (opens in a new tab)

  6. Targeting the Tumor Stroma Using a Monoclonal Antibody Platform Technology

    … the discovery and validation of a monoclonal antibody that selectively binds to FAP. The lead antibody, B12, was identified from a naïve murine single-chain variable fragment antibody phage display library screened against recombinant human FAP. The heavy and light chains of B12 were cloned …

    umn Repository record for Targeting the Tumor Stroma Using a Monoclonal Antibody Platform Technology (opens in a new tab)

  7. Design of smart linkers and their applications in controlled-release drug delivery systems

    Antibody drug conjugates (ADC) represents an interesting strategy in tumour targeted therapy . The approach is based on the combination of the high affinity of an antibody towards its antigen and the high cytotoxicity of a drug, leading to a selective therapuetic agent with improved efficacy and …

    dialnet Repository record for Design of smart linkers and their applications in controlled-release drug delivery systems (opens in a new tab)

  8. Generation and therapeutic evaluation of recombinant immunotherapeutics on CD64+ monocytic cell lines and polarized ex vivo differentiated human macrophages

    … population. Methods: The CD64-targeting antibody fragment (H22(scFv)) was used to generate; 1) a recombinant immunotoxin (rIT) through genetic fusion with the enzymatic domain of Pseudomonas aeruginosa exotoxin A (ETA`), or 2) a SNAP-tag fusion protein (FP) to allow chemical coupling of …

    cape-town Repository record for Generation and therapeutic evaluation of recombinant immunotherapeutics on CD64+ monocytic cell lines and polarized ex vivo differentiated human macrophages (opens in a new tab)

  9. Strategy for Controlled Protection of Redox-Cycling Ortho-Quinones with Self-Immolative Linkers

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    cambridge