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https://read.qxmd.com/read/36230591/ethanol-ablation-therapy-drives-immune-mediated-antitumor-effects-in-murine-breast-cancer-models
#1
JOURNAL ARTICLE
Corrine A Nief, Adam M Swartz, Erika Chelales, Lauren Y Sheu, Brian T Crouch, Nirmala Ramanujam, Smita K Nair
Ethanol ablation is a minimally invasive, cost-effective method of destroying tumor tissue through an intratumoral injection of high concentrations of cytotoxic alcohol. Ethyl-cellulose ethanol (ECE) ablation, a modified version of ethanol ablation, contains the phase-changing polysaccharide ethyl-cellulose to reduce ethanol leakage away from the tumor. Ablation produces tissue necrosis and initiates a wound healing process; however, the characteristic of the immunologic events after ECE ablation of tumors has yet to be explored...
September 25, 2022: Cancers
https://read.qxmd.com/read/34966967/effect-of-alpha-fetoprotein-on-differentiation-of-myeloid-supressor-cells
#2
JOURNAL ARTICLE
S A Zamorina, K Yu Shardina, V P Timganova, M S Bochkova, S V Uzhviyuk, M B Raev, V A Chereshnev
The effect of recombinant alpha-fetoprotein (AFP) on human myeloid suppressor cell (MDSC) differentiation was studied in vitro in the presence of cytokines IL-6 (10 ng/mL) and GM-CSF (10 ng/mL). It was found that AFP at concentrations of 50 and 100 IU/mL increased the number of MDSC (CD33+ HLA-DR-/low CD11b+ ) in culture. Analysis of MDSC subpopulations showed that the increase was due to monocytic M-MDSC (HLA-DR-/low CD33+ CD11b+ CD14+ CD66b- ). There was no modulating effect of AFP on granulocytic PMN-MDSC (HLA-DR-/low CD33+ CD11b+ CD14- CD66b+ )...
November 2021: Doklady. Biochemistry and Biophysics
https://read.qxmd.com/read/27694385/tumor-cell-independent-estrogen-signaling-drives-disease-progression-through-mobilization-of-myeloid-derived-suppressor-cells
#3
JOURNAL ARTICLE
Nikolaos Svoronos, Alfredo Perales-Puchalt, Michael J Allegrezza, Melanie R Rutkowski, Kyle K Payne, Amelia J Tesone, Jenny M Nguyen, Tyler J Curiel, Mark G Cadungog, Sunil Singhal, Evgeniy B Eruslanov, Paul Zhang, Julia Tchou, Rugang Zhang, Jose R Conejo-Garcia
The role of estrogens in antitumor immunity remains poorly understood. Here, we show that estrogen signaling accelerates the progression of different estrogen-insensitive tumor models by contributing to deregulated myelopoiesis by both driving the mobilization of myeloid-derived suppressor cells (MDSC) and enhancing their intrinsic immunosuppressive activity in vivo Differences in tumor growth are dependent on blunted antitumor immunity and, correspondingly, disappear in immunodeficient hosts and upon MDSC depletion...
January 2017: Cancer Discovery
https://read.qxmd.com/read/21153863/decitabine-induced-apoptosis-is-derived-by-puma-and-noxa-induction-in-chronic-myeloid-leukemia-cell-line-as-well-as-in-pbl-and-is-potentiated-by-saha
#4
JOURNAL ARTICLE
Barbora Brodská, Petra Otevřelová, Aleš Holoubek
Restoration of cellular apoptotic pathways plays a crucial role in cancer therapy strategies. In a broad spectrum of anticancer drugs, epigenetic effectors are in the center of interest mostly because of potential reversibility of their action. Methylation status of the cells is influenced by methyltransferase inhibitor 2-deoxy-5'-azacytidine (decitabine, DAC), but higher concentrations of this agent cause a DNA-damage. In our study, tumor supressor p53-apoptotic pathway was activated in decitabine-induced cell death...
April 2011: Molecular and Cellular Biochemistry
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