Histone deacetylase 6 regulates the immunosuppressive properties of cancer-associated fibroblasts in breast cancer through the STAT3–COX2-dependent pathway
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Title
Histone deacetylase 6 regulates the immunosuppressive properties of cancer-associated fibroblasts in breast cancer through the STAT3–COX2-dependent pathway
Authors
Keywords
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Journal
ONCOGENE
Volume -, Issue -, Pages -
Publisher
Springer Nature
Online
2018-07-06
DOI
10.1038/s41388-018-0379-9
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- (2017) Nikolaos G. Frangogiannis JOURNAL OF CLINICAL INVESTIGATION
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- (2016) Miłosz Regulski et al. DRUG DISCOVERY TODAY
- Epigenetic modifiers in immunotherapy: a focus on checkpoint inhibitors
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- (2016) Vinit Kumar et al. TRENDS IN IMMUNOLOGY
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- (2015) Y. Sharon et al. CANCER RESEARCH
- HDAC6 mediates HIV-1 tat-induced proinflammatory responses by regulating MAPK-NF-kappaB/AP-1 pathways in astrocytes
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- Depletion of Carcinoma-Associated Fibroblasts and Fibrosis Induces Immunosuppression and Accelerates Pancreas Cancer with Reduced Survival
- (2014) Berna C. Özdemir et al. CANCER CELL
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- A Novel Role for Histone Deacetylase 6 in the Regulation of the Tolerogenic STAT3/IL-10 Pathway in APCs
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- Targeting cardiac fibroblasts to treat fibrosis of the heart: Focus on HDACs
- (2014) Katherine B. Schuetze et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Divergent roles of histone deacetylase 6 (HDAC6) and histone deacetylase 11 (HDAC11) on the transcriptional regulation of IL10 in antigen presenting cells
- (2014) Fengdong Cheng et al. MOLECULAR IMMUNOLOGY
- Eradication of metastatic mouse cancers resistant to immune checkpoint blockade by suppression of myeloid-derived cells
- (2014) K. Kim et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Targeting CXCL12 from FAP-expressing carcinoma-associated fibroblasts synergizes with anti-PD-L1 immunotherapy in pancreatic cancer
- (2013) C. Feig et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- COX2 regulation of breast cancer bone metastasis
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- Enzymatic Targeting of the Stroma Ablates Physical Barriers to Treatment of Pancreatic Ductal Adenocarcinoma
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- (2012) Elizabeth S. Nakasone et al. CANCER CELL
- Hyaluronan impairs vascular function and drug delivery in a mouse model of pancreatic cancer
- (2012) Michael A Jacobetz et al. GUT
- Prostaglandin E2 EP receptors as therapeutic targets in breast cancer
- (2011) Jocelyn Reader et al. CANCER AND METASTASIS REVIEWS
- Bone morphogenetic protein (BMP) signaling regulates mitotic checkpoint protein levels in human breast cancer cells
- (2011) Hualong Yan et al. CELLULAR SIGNALLING
- NF-κB Signaling Pathway, Inflammation and Colorectal Cancer
- (2010) Soly Wang et al. Cellular & Molecular Immunology
- Lysine Acetylation Targets Protein Complexes and Co-Regulates Major Cellular Functions
- (2009) C. Choudhary et al. SCIENCE
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