| Vol. 12.05 – 11 February, 2021 |
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| The diabetic interstitium was enriched for ECM organization and small-molecule catabolism. Cell type markers with unchanged expression and those down-regulated in diabetic nephropathy were identified. [Science Advances] |
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| PUBLICATIONSRanked by the impact factor of the journal |
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| The authors describe how MSCs could be used to systemically deliver a binary vector containing an oncolytic adenovirus (Ad) together with a helper dependent Ad that expresses IL-12 and checkpoint PD-L1 blocker. [Molecular Therapy] |
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| Investigators systematically analyzed proteomics of decellularized hepatic matrix and identified four unique clusters of ECM proteins at tissue damage/inflammation, transitional ECM remodeling or fibrogenesis stage in carbon tetrachloride-induced liver fibrosis. [Cell Death & Disease] |
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| LAMA2 encodes laminin-α2, a subunit of the trimeric laminin-211 ECM protein that is the predominant laminin expressed in skeletal muscle. LAMA2 expression stabilized skeletal muscle, in part by binding membrane receptors via its five globular (G) domains. Researchers tested the therapeutic efficacy of these G1-G5 domains in the dyW mouse model for MDC1A. [Molecular Therapy-Methods & Clinical Development] |
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| Scientists’ multi-day, time-lapse imaging data provided detailed visualizations of evolving spheroid morphology, collagen degradation, and collagen deformation, all using label-free scattering contrast. [Scientific Reports] |
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| Researchers showed both EZH2 expression and its enzymatic activity were significantly increased in ECM detached cancer cells when compared to the attached cells. Inhibition of EZH2 resulted in a significant reduction in cell proliferation, spheroids size, and induction in apoptosis in ECM detached cells. [Scientific Reports] |
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| The authors investigated the cancer stem cell‐promoting effect of factors released from myofibroblasts into the microenvironment of early colorectal cancer tumors and its molecular mechanism. [Molecular Carcinogenesis] |
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| Emerging evidence indicates an important role for the tissue microenvironment in the pathogenesis of rheumatoid arthritis (RA). Each tissue is made up of cells surrounded and supported by a unique ECM. These complex molecular networks define tissue architecture and provide environmental signals that program site-specific cell behavior. [Nature Reviews Rheumatology] |
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| Investigators provide an overview of the challenges of examining ATP generation and delivery within invading cells and how recent studies using diverse invasion models, experimental approaches, and energy biosensors are revealing that energy metabolism is an integral component of cell invasive behavior that is dynamically tuned to overcome the ECM environment. [Trends in Cell Biology] |
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| The authors focus on important role of tumor-intrinsic factors and tumor microenvironment in driving partial epithelial-to-mesenchymal transition (pEMT) and emphasize that engineered controlled microenvironments are instrumental to provide mechanistic insights into pEMT biology. [iScience] |
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| Arch Oncology, Inc. announced that it has entered into a clinical trial collaboration and supply agreement with Merck. Under this collaboration, Arch Oncology is expanding its ongoing Phase I/II clinical trial to evaluate AO-176, the Company’s novel anti-CD47 antibody, in combination with KEYTRUDA® (pembrolizumab), Merck’s anti-PD-1 therapy, for the treatment of patients with select solid tumors. [Arch Oncology, Inc.] |
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| May 18 – 21, 2021 Virtual |
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| Merck Sharp and Dohme Limited – London, England, United Kingdom |
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| Oklahoma Medical Research Foundation – Oklahoma City, Oklahoma, United States |
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| Blood Research Institute – Milwaukee, Wisconsin, United States |
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| The University of British Columbia – Vancouver, British Columbia, Canada |
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| Rutgers Cancer Institute of New Jersey – Rutgers, New Jersey, United States |
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