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Gilmore, N.

Publications and source records attributed to Gilmore, N..

2 recordsLinked to original sources

The neural correlates of novel versus familiar metaphors in healthy young adults: A functional near-infrared spectroscopy study

Despite extensive investigation, the neural correlates of metaphor processing remain debated. Poor theoretical and experimental control of variables that drive metaphor activation-- particularly the constructs of novelty and familiarity--may be the reason for past discrepancies between studies. To address this issue, we used functional near-infrared spectroscopy (fNIRS) and a carefully designed paradigm modified from Cardillo et al. (2012) to investigate how neural activation varies by sentence type (metaphorical versus literal sentences) and novelty (completely novel versus familiarized phrases). Activity was significantly greater for metaphorical over literal sentences in the left inferior frontal gyrus, pars triangularis (LIFGtri), left inferior parietal cortex, right IFG, pars opercularis (RIFGop), and right angular gyrus (RAG). Novel metaphors to which participants had no prior exposure had significantly higher (albeit weak) effects within RIFGop, RAG, and right middle temporal gyrus (RMTG) compared to novel metaphors to which participants were exposed just prior to the fNIRS experiment. Pre-exposed, more familiar metaphors significantly activated a wider network of regions compared to novel metaphors, including bilateral middle frontal gyrus (MFG), bilateral IFGtri, and LMTG. A greater response time difference between conditions was associated with less LMFG activity for metaphors over literal sentences but higher LMTG activity for novel over more familiar metaphors. Taken together, these findings suggest that metaphors--particularly novel metaphors--do engage right hemisphere cortex more than other phrase types (literal sentences, more familiar metaphors) but that the effects are weaker than condition differences within canonical left language network and domain-general multiple demand network regions.

neuroscience↗

Hyaluronidase inhibitor delphinidin inhibits cancer metastasis

Cancer remains a formidable global health challenge, with metastasis being a key contributor to its lethality. Abundant high molecular mass hyaluronic acid, a major non-protein component of extracellular matrix, protects naked mole rats from cancer and reduces cancer incidence in mice. Hyaluronidase plays a critical role in degrading hyaluronic acid and is frequently overexpressed in metastatic cancer. Here we investigated the potential of targeting hyaluronidases to reduce metastasis. High throughput screen identified delphinidin, a natural plant compound found in fruits and vegetables, as a potent hyaluronidase inhibitor. Delphinidin-mediated inhibition of hyaluronidase activity led to an increase in high molecular weight hyaluronic acid in cell culture and in mouse tissues, and reduced migration and invasion behavior of breast, prostate, and melanoma cancer cells. Moreover, delphinidin treatment suppressed melanoma metastasis in mice. Our study provides a proof of principle that inhibition of hyaluronidase activity suppresses cancer cell migration, invasion and metastasis. Furthermore, we identify a natural compound delphinidin as a potential anticancer therapeutic. Thus, we have identified a path for clinical translation of the cancer resistance mechanism identified in the naked mole rat.

cancer biology↗