A
Anisha A. Gupte
Researcher at Houston Methodist Hospital
Publications - 49
Citations - 2027
Anisha A. Gupte is an academic researcher from Houston Methodist Hospital. The author has contributed to research in topics: Insulin & Skeletal muscle. The author has an hindex of 22, co-authored 44 publications receiving 1562 citations. Previous affiliations of Anisha A. Gupte include Kansas State University & Cornell University.
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Journal ArticleDOI
Cholesterol Induces CD8+ T Cell Exhaustion in the Tumor Microenvironment
Xingzhe Ma,Enguang Bi,Yong Lu,Pan Su,Chunjian Huang,Lintao Liu,Qiang Wang,Maojie Yang,Matthew F. Kalady,Jianfei Qian,Aijun Zhang,Anisha A. Gupte,Dale J. Hamilton,Chengyun Zheng,Qing Yi +14 more
TL;DR: It is reported that cholesterol in the tumor microenvironment induces CD8+ T cell expression of immune checkpoints and exhaustion and a new strategy for restoring T-cell function by reducing cholesterol to enhance T cell-based immunotherapy is suggested.
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Heat Treatment Improves Glucose Tolerance and Prevents Skeletal Muscle Insulin Resistance in Rats Fed a High-Fat Diet
TL;DR: The results indicate that heat treatment protects skeletal muscle from high-fat diet–induced insulin resistance and provide strong evidence that HSP induction in skeletal muscle could be a potential therapeutic treatment for obesity- induced insulin resistance.
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Estrogen: An Emerging Regulator of Insulin Action and Mitochondrial Function
TL;DR: Clinical trials and animal studies reveal that loss of circulating estrogen induces rapid changes in whole body metabolism, fat distribution, and insulin action, and recent investigations suggest that estrogen receptor-α elicits the metabolic effects of estrogen by genomic, nongenomic, and mitochondrial mechanisms that regulate insulin signaling, substrate oxidation, and energetics.
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Nuclear factor (erythroid-derived 2)-like-2 factor (Nrf2), a key regulator of the antioxidant response to protect against atherosclerosis and nonalcoholic steatohepatitis.
TL;DR: Macrophage-selective Nrf2 activation may provide an approach to reduce vascular and hepatocyte injury without the complications of systemic antioxidants, since macrophages play key roles in the development and progression of both atherosclerosis and NASH.
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Age-related differences in skeletal muscle insulin signaling: the role of stress kinases and heat shock proteins
TL;DR: A greater constitutive HSP expression and lower stress kinase activation may account for the ability of slow-twitch muscles to preserve the capacity to respond to insulin and maintain glucose homeostasis with age.