ArticleAnnals of medicine and surgery (2012)2026
Significant anti-myeloma potential of green tea infusion and its component dihydromyricetin.
Article in Annals of medicine and surgery (2012), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Abstract
Multiple myeloma (MM) is a fatal hematological malignancy characterized by overgrowth of monoclonal plasma cells. Although green tea exhibits well-documented antitumor properties, its specific effects against MM remain poorly characterized. This study aimed to investigate the anti-myeloma activity of infusions from four representative green teas and identify their effective components. We found that apoptosis of MM cells was induced by green tea infusions in a concentration-dependent manner, with Biluochun tea infusion showing the most potent efficacy. An animal study showed that Biluochun tea infusion significantly reduced MM tumor size, downregulated the proliferation marker Ki-67, and increased TUNEL-positive apoptotic cells in MM tumor tissues. Furthermore, mass spectrometry analysis identified dihydromyricetin (DMY) as a pivotal distinguishing component of Biluochun among the four tea infusions. As expected, DMY induced apoptosis in MM cells in a concentration-dependent manner, accompanied by decreased mitochondrial membrane potential and elevated expression of cleaved caspase-3 and caspase-8. These findings indicate that DMY elicits anti-myeloma effects through activation of both the intrinsic mitochondrial and extrinsic apoptotic pathways. Collectively, this study provides preliminary preclinical evidence supporting the anti-myeloma activity of DMY in cell and xenograft mouse models, which lays a foundation for subsequent translational research exploring green tea-derived compounds against MM; further multilayered validation is required to confirm its clinical value.
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