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Lin Luo

Researcher at Nantong University

Publications -  15
Citations -  155

Lin Luo is an academic researcher from Nantong University. The author has contributed to research in topics: Immune system & FOXP3. The author has an hindex of 6, co-authored 13 publications receiving 79 citations. Previous affiliations of Lin Luo include University of Alabama at Birmingham & Sichuan University.

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Rosuvastatin improves myocardial hypertrophy after hemodynamic pressure overload via regulating the crosstalk of Nrf2/ARE and TGF-β/ smads pathways in rat heart.

TL;DR: Results revealed the crosstalk between TGF‐&bgr;1/Smads and Nrf2/ antioxidant response elements (ARE) pathways in myocardial remodeling through the interaction between Smad7 and NRF2.
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Remodeling of the tumor microenvironment via disrupting Blimp1+ effector Treg activity augments response to anti-PD-1 blockade.

TL;DR: In this article, the effect of Foxp3-specific ablation of Blimp1 in Treg cells resulted in impaired suppressive activity and a reprogramming into effector T-cells, which were largely restricted to the tumor-infiltrating Treg population.
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A novel harmine derivative, N-(4-(hydroxycarbamoyl)benzyl)-1-(4- methoxyphenyl)-9H-pyrido[3,4-b]indole-3-carboxamide (HBC), as histone deacetylase inhibitor: in vitro antiproliferation, apoptosis induction, cell cycle arrest, and antimetastatic effects.

TL;DR: Novel harmine‐based HDAC inhibitor HBC not only exhibited selective HDAC1/6 inhibitory activity and significant in vitro and in vivo antitumor activity, but also possessed DNA binding effect, apoptosis induction, cell cycle arrest effects, and potent anti‐metastasis mechanisms, which may hold great promise as therapeutic agent targeting HDAC 1/6 for the intervention of human cancers.
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bFGF overexpression adipose derived mesenchymal stem cells improved the survival of pulmonary arterial endothelial cells via PI3k/Akt signaling pathway.

TL;DR: In this article, bFGF transfected mesenchymal stem cells (ASCs) improved the survival of human pulmonary arterial endothelial cells (HPAECs) by activating the PI3k/Akt pathway.