| Vol. 13.20 – 24 May, 2022 |
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Hesperadin Suppresses Pancreatic Cancer through ATF4/GADD45A Axis at Nanomolar Concentrations | Scientists identified Hesperadin as a potent anti-cancer compound against pancreatic cancer, from a high-throughput screening of a commercial chemical library associated with cell death. [Oncogene] |
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PUBLICATIONSRanked by the impact factor of the journal |
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NF-κB-Inducing Kinase (NIK) Is Activated in Pancreatic β-Cells but Does Not Contribute to the Development of Diabetes | Investigators showed that genetic silencing of NIK in pancreatic β-cells neither modified diabetes incidence nor inflammatory responses in a mouse model of immune-mediated diabetes. [Cell Death & Disease] |
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A Saponin from Astragalus Promotes Pancreatic Ductal Organoids Differentiation into Insulin-Producing Cells | The authors established mouse pancreatic ductal organoids with progenitor characteristics and an insulin promoter-driven enhanced green fluorescent protein reporter system to screen astragalus saponin components for monomers that could promote insulin-producing cell differentiation. [Phytomedicine] |
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Ginsenoside Rg3 Ameliorates Acute Pancreatitis by Activating the NRF2/HO-1-Mediated Ferroptosis Pathway | An in vitro acute pancreatitis cell model was established in the present study by exposing AR42J cells to cerulein (Cn). AR42J cell viability was increased in the Rg3‑treated group as compared with the Cn‑exposed group. [International Journal of Molecular Medicine] |
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NNK from Tobacco Smoking Enhances Pancreatic Cancer Cell Stemness and Chemoresistance by Creating a β2AR-Akt Feedback Loop That Activates Autophagy | The authors found that 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) promoted stemness and gemcitabine resistance in pancreatic cancer cell lines. [Molecular Oncology] |
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Transcriptional ITPR3 as Potential Targets and Biomarkers for Human Pancreatic Cancer | Researchers examined the expression levels and survival dates of Inositol 1,4,5-Triphosphate Receptor Family (ITPRs) in patients with pancreatic cancer. As a result, they identified that ITPR1 and ITPR3 expression levels were significantly elevated in cancerous specimens. [Aging] |
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Butyrate, a Postbiotic of Intestinal Bacteria, Affects Pancreatic Cancer and Gemcitabine Response in In Vitro and In Vivo Models | Scientists provided in vitro evidence that, in addition to slowing proliferation, butyrate enhanced gemcitabine effectiveness against two human pancreatic cancer cell lines, mainly inducing apoptosis. [Biomedicine & Pharmacotherapy] |
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Photoimmunotherapy Retains Its Anti-Tumor Efficacy with Increasing Stromal Content in Heterotypic Pancreatic Cancer Spheroids | Investigators provided a systematic evaluation of photodynamic therapy in 3D heterotypic coculture models of PDAC with varying ratios of patient-derived pancreatic cancer-associated fibroblasts that simulated heterogeneous PDAC tumors with increasing stromal content. [Molecular Pharmaceutics] |
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Sparstolonin B Inhibits Pancreatic Adenocarcinoma through the NF-κB Signaling Pathway | Sparstolonin B significantly decreased Panc-1 and SW1990 cell viability and effectively suppressed the proliferation, migration, and invasion of pancreatic cancer cells as shown by CCK-8, colony formation, and Transwell assays. [Experimental Cell Research] |
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Nanoparticle-Based Therapeutic Strategies Targeting Major Clinical Challenges in Pancreatic Cancer Treatment | The authors focus on the pathological hallmarks of PDAC and the impact of nanotechnology to find solutions, describing the use of nanoparticle-based systems designed for the delivery of chemotherapeutic agents and combinatorial alternatives that address the chemoresistance associated with PDAC. [Advanced Drug Delivery Reviews] |
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Exosomes and Their Roles in the Chemoresistance of Pancreatic Cancer | Investigators focus on the intrinsic connections between the chemoresistance of pancreatic cancer cells and exosomes in the tumor microenvironment. [Cancer Medicine] |
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PharmaCyte Biotech Initiates Studies to Confirm Its Pancreatic Cancer Therapy Can Treat Malignant Ascites | PharmaCyte Biotech, Inc. announced that it has initiated the first in a series of studies to test the ability of its pancreatic cancer therapy to treat malignant ascites. [PharmaCyte Biotech, Inc.] |
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| London, England, United Kingdom |
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| Rutgers Robert Wood Johnson Medical School – New Brunswick, New Jersey, United States |
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| City of Hope – Duarte, California, United States |
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| City of Hope – Duarte, California, United States |
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| Steno Diabetes Center – Herlev, Denmark |
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