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Tran, M. G.

Publications and source records attributed to Tran, M. G..

2 recordsLinked to original sources

Striatal D2-neurons gate D1-mediated associative encoding under uncertainty

Goal-directed actions are established through the encoding of predictive relationships between behaviour and its consequences, a process involving dopamine-dependent plasticity in the dorsal striatum. Early phases of learning entail complex associative landscapes from which useful action-outcome contingencies must be identified. Although dopamine processes are central to associative learning, the cellular mechanisms through which behaviourally relevant plasticity is selected from competing signalling events remain unknown. Here we show that D2-spiny projection neurons (D2-SPNs) are transiently recruited during the earliest stages of instrumental learning, when critical action-outcome contingencies emerge. We identify a dominant cell-to-cell transmodulation process by which D2-SPNs regulate dopamine-dependent signalling by constraining protein kinase A activity in D1-SPNs. This mechanism overrides extracellular dopamine signals and can be reproduced in vivo through calibrated optogenetic activation of cAMP signalling. Enhancing D2[->]D1-SPN transmodulation during uncertain reinforcement schedules durably improves action-outcome encoding, revealing a mechanism through which striatal networks promote relevant contingencies under associative ambiguity.

neuroscience↗

Independence of HIF1a and androgen signaling pathways in prostate cancer

Androgen signaling drives prostate cancer progression and is a therapeutic target. Hypoxia/HIF1a signaling is associated with resistance to hormone therapy and a poor prognosis in patients treated with surgery or radiotherapy. It is not known whether the pathways operate in cooperation or independently. Using LNCaP cells with and without stable transfection of a HIF1a expression vector, we show that combined AR and HIF1a signaling promotes tumor growth in vitro and in vivo, and the capacity of HIF1a to promote tumor growth in the absence of endogenous androgen in vivo. Gene expression analysis identified 7 genes that were upregulated by both androgen and HIF1a. ChIP-Seq analysis showed that the AR and HIF/hypoxia signaling pathways function independently regulating the transcription of different genes with few shared targets. In clinical datasets elevated expression of 5 of the 7 genes was associated with a poor prognosis. Our findings suggest that simultaneous therapeutic inhibition of AR and HIF1a signaling pathways should be explored as a potential therapeutic strategy.

cancer biology↗