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Tennekoon, K. H.

Publications and source records attributed to Tennekoon, K. H..

2 recordsLinked to original sources

Distinct trajectories of urbanization shape the human gut microbiome across South Asia

Human gut microbiomes respond to lifestyle transitions, yet the extent to which these responses are conserved across spatio-cultural contexts remains undercharacterized. We present the South Asian MicroBiome ARray (SAMBAR), a population-scale 16S gut microbiome study of 575 adults from ten geographically and socio-culturally diverse South Asian communities. Each community was sampled in ancestral villages and urban centers, enabling controlled comparisons of geography and lifestyle. Relative to global cohorts, SAMBAR microbiomes occupy a distinct compositional space with stronger correlation to geography and community membership than lifestyle. Although urbanization is consistently associated with increased abundance of disease-linked taxa, microbiome responses to lifestyle transitions are largely community-driven, including the acquisition of wheat- and dairying-associated microbial modules in some communities that may facilitate non-genetic adaptation to lactase non-persistence. Microbiome responses to urbanization are heterogeneous even at regional scales, reflecting local culture and geography and underscoring the need for community-specific investigations of health impacts.

microbiology↗

Anti-proliferative and Apoptosis Inducing Effect of Thymoquinone in Human Teratocarcinomal (NTERA-2) Cancer Stem-Like Cells

Cancer stem cells (CSCs) are key drivers of tumor progression, therapeutic resistance and recurrence. Nigella sativa, a medicinal plant widely used in traditional medicine, has gained significant importance due to its diverse pharmacological properties. Thymoquinone (TQ), a biologically known active compound isolated from N.sativa, has demonstrated anticancer properties in various cancers. However, its effect on CSC-like cells has not been fully elucidated. In the present study, the anti-proliferative and apoptosis inducing properties of TQ was evaluated on human embryonal carcinoma cells (NTERA-2, cancer stem cell like model) and human peripheral blood mononuclear cells (PBMCs) in vitro. Antiproliferative effects of TQ on NTERA-2 cells and PBMCs were evaluated using the Sulforhodamine B (SRB) and WST-1 assays, respectively. The effect of TQ was further evaluated using colony formation assay, cell migration assay, fluorescence microscopy and quantification of caspase 3/7 activities. Oxidative stress markers (reactive oxygen species [ROS]) were also determined in NTERA-2 cells treated with TQ. Thymoquinone revealed promising dose- and time-dependent antiproliferative effects (half-maximal inhibitory concentration [IC50] 1.282, 1.167, and 0.984 g/mL at 24, 48, and 72 h post-treatment) in NTERA-2 cells while exerting a minimal cytotoxic effect in PBMCs. Apoptosis related morphological changes, and increased Caspase 3/7 activities confirmed the pro-apoptotic effects of TQ. Further, NTERA-2 cells treated with TQ expressed a significant increase (P < 0.001) in intracellular ROS activity. Overall results confirm that TQ exerts anti-proliferative and apoptotic effects in a dose- and time-dependent manner. Therefore, TQ can be considered as a potent drug lead for chemotherapy and radiotherapy resistant cancer stem cells.

pharmacology and toxicology↗