Publications by authors named "J L Chuang"

Limosilactobacillus reuteri is a probiotic bacterium known for its numerous beneficial effects on human health and is commonly utilized in various dietary supplements. Previously, we encountered difficulties in isolating L. reuteri from retail dietary supplements containing complex probiotic compositions by using non-selective media such as de Man, Rogosa, and Sharpe (MRS) agar.

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Colorectal cancer is a leading cause of cancer-related morbidity and mortality worldwide, with more than 1.9 million new cases reported in 2020, and is associated with major survival challenges, particularly in patients with locally advanced colon cancer (LACC). LACC often involves T4 invasion or extensive nodal involvement and requires a multidisciplinary approach for management.

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Resistance of BRAF-mutant melanomas to targeted therapy arises from the ability of cells to enter a persister state, evade treatment with relative dormancy, and repopulate the tumor when reactivated. A better understanding of the temporal dynamics and specific pathways leading into and out of the persister state is needed to identify strategies to prevent treatment failure. Using spatial transcriptomics in patient-derived xenograft models, we captured clonal lineage evolution during treatment.

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While reactive oxygen species (ROS) have long been known to drive aging and neurodegeneration, their persistent depletion below basal levels also disrupts organismal function. Cells counteract loss of basal ROS via the reductive stress response, but the identity and biochemical activity of ROS sensed by this pathway remain unknown. Here, we show that the central enzyme of the reductive stress response, the E3 ligase Cullin 2-FEM1 homolog B (CUL2), specifically acts at mitochondrial TOM complexes, where it senses ROS produced by complex III of the electron transport chain (ETC).

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Article Synopsis
  • Glioblastoma (GBM) is a difficult-to-treat brain cancer characterized by aggressive behavior and high rates of recurrence, with tumor-associated microglia and macrophages (TAM) playing a significant role in its immune microenvironment.
  • Researchers found that TAMs in the tumor core show higher ATP synthase expression and activity, leading to increased energy production and metabolic changes in the presence of GBM cells, which in turn stimulate tumor growth.
  • Targeting the signaling pathway involving elevated extracellular ATP (eATP) and the P2X purinoceptor 7 (P2X7R) has the potential to decrease tumor growth and improve survival rates in models of GBM, highlighting a new therapeutic strategy.
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