scispace - formally typeset
T

Tanaya Shree

Researcher at Stanford University

Publications -  24
Citations -  1439

Tanaya Shree is an academic researcher from Stanford University. The author has contributed to research in topics: Medicine & Immune system. The author has an hindex of 8, co-authored 16 publications receiving 1224 citations. Previous affiliations of Tanaya Shree include University of Ottawa & Memorial Sloan Kettering Cancer Center.

Papers
More filters
Journal ArticleDOI

IL-4 induces cathepsin protease activity in tumor-associated macrophages to promote cancer growth and invasion

TL;DR: It is demonstrated that high levels of cathepsin protease activity are induced in the majority of macrophages in the microenvironment of pancreatic islet cancers, mammary tumors, and lung metastases during malignant progression and that interleukin-4 (IL-4) is responsible for inducing cat hepsin activity in macrophage in vitro and in vivo.
Journal ArticleDOI

Macrophages and cathepsin proteases blunt chemotherapeutic response in breast cancer

TL;DR: Increased macrophage infiltration and cathepsin protease levels in mammary tumors following paclitaxel (Taxol) chemotherapy are found and this study highlights the importance of integrated targeting of the tumor and its microenvironment and implicates macrophages andCathepsins in blunting chemotherapeutic response.
Journal ArticleDOI

Regulation of Dopaminergic Loss by Fas in a 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine Model of Parkinson's Disease

TL;DR: Although critical for degeneration of the soma, Fas deficiency did not significantly prevent the reduction of dopaminergic terminal fibers within the striatum or normalize the activation of striatal microglia and elevation of the postsynaptic activity marker ΔFosB induced by denervation.
Journal ArticleDOI

Identification and pre-clinical testing of a reversible cathepsin protease inhibitor reveals anti-tumor efficacy in a pancreatic cancer model

TL;DR: The identification of VBY-825 as a new and effective anti-tumor drug encourages the therapeutic application of cathepsin inhibitors in cancer.
Journal ArticleDOI

Interaction of the c-Jun/JNK pathway and cyclin-dependent kinases in death of embryonic cortical neurons evoked by DNA damage.

TL;DR: C-Jun/JNK is activated following DNA damage and it is proposed that c-Jun is regulated by the JNK and CDK pathways and that both must be activated for efficient c- Jun activation to occur.