Inhibition of heat shock protein (HSP) 90 reverses signal transducer and activator of transcription (STAT) 3‐mediated muscle wasting in cancer cachexia mice
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Title
Inhibition of heat shock protein (HSP) 90 reverses signal transducer and activator of transcription (STAT) 3‐mediated muscle wasting in cancer cachexia mice
Authors
Keywords
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Journal
BRITISH JOURNAL OF PHARMACOLOGY
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2021-07-16
DOI
10.1111/bph.15625
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Note: Only part of the references are listed.- ARRIVE 2.0 and the British Journal of Pharmacology: Updated guidance for 2020
- (2020) Elliott Lilley et al. BRITISH JOURNAL OF PHARMACOLOGY
- The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research
- (2020) Nathalie Percie du Sert et al. PLOS BIOLOGY
- CiiiDER: A tool for predicting and analysing transcription factor binding sites
- (2019) Linden J. Gearing et al. PLoS One
- HuR counteracts miR-330 to promote STAT3 translation during inflammation-induced muscle wasting
- (2019) Souad Mubaid et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Heat Shock Proteins: Agents of Cancer Development and Therapeutic Targets in Anti-Cancer Therapy
- (2019) Chul Won Yun et al. Cells
- Goals and practicalities of immunoblotting and immunohistochemistry: A guide for submission to the British Journal of Pharmacology
- (2018) Steve P H Alexander et al. BRITISH JOURNAL OF PHARMACOLOGY
- Experimental design and analysis and their reporting II: updated and simplified guidance for authors and peer reviewers
- (2018) Michael J Curtis et al. BRITISH JOURNAL OF PHARMACOLOGY
- HSP-enriched properties of extracellular vesicles involve survival of metastatic oral cancer cells
- (2018) Kisho Ono et al. JOURNAL OF CELLULAR BIOCHEMISTRY
- Targeting the IL-6/JAK/STAT3 signalling axis in cancer
- (2018) Daniel E. Johnson et al. Nature Reviews Clinical Oncology
- Modulating Metabolism to Improve Cancer-Induced Muscle Wasting
- (2018) Fabio Penna et al. Oxidative Medicine and Cellular Longevity
- STAT3 in Skeletal Muscle Function and Disorders
- (2018) Eleonora Guadagnin et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- FoxO Transcription Factors are Critical Regulators of Diabetes-Related Muscle Atrophy
- (2018) Brian T. O’Neill et al. DIABETES
- S1PR1 predicts patient survival and promotes chemotherapy drug resistance in gastric cancer cells through STAT3 constitutive activation
- (2018) Shiyu Song et al. EBioMedicine
- The HSP90 chaperone machinery
- (2017) Florian H. Schopf et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY
- (2017) Simon D Harding et al. NUCLEIC ACIDS RESEARCH
- Luteolin selectively kills STAT3 highly activated gastric cancer cells through enhancing the binding of STAT3 to SHP-1
- (2017) Shiyu Song et al. Cell Death & Disease
- Pantoprazole blocks the JAK2/STAT3 pathway to alleviate skeletal muscle wasting in cancer cachexia by inhibiting inflammatory response
- (2017) Dunwei Guo et al. Oncotarget
- The ubiquitin proteasome system in atrophying skeletal muscle: roles and regulation
- (2016) Philippe A. Bilodeau et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- STAT3 in the systemic inflammation of cancer cachexia
- (2016) Teresa A. Zimmers et al. SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
- Inhibition of Stat3 Activation Suppresses Caspase-3 and the Ubiquitin-Proteasome System, Leading to Preservation of Muscle Mass in Cancer Cachexia
- (2015) Kleiton Augusto Santos Silva et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Regulation of autophagy and the ubiquitin–proteasome system by the FoxO transcriptional network during muscle atrophy
- (2015) Giulia Milan et al. Nature Communications
- Sunitinib prevents cachexia and prolongs survival of mice bearing renal cancer by restraining STAT3 and MuRF-1 activation in muscle
- (2015) Francesca Pretto et al. Oncotarget
- Myostatin Gene Inactivation Prevents Skeletal Muscle Wasting in Cancer
- (2014) Y. S. Gallot et al. CANCER RESEARCH
- Stat3 Activation Links a C/EBPδ to Myostatin Pathway to Stimulate Loss of Muscle Mass
- (2013) Liping Zhang et al. Cell Metabolism
- Skeletal muscle glycoprotein 130's role in Lewis lung carcinoma–induced cachexia
- (2013) Melissa J. Puppa et al. FASEB JOURNAL
- Selective androgen receptor modulators in cancer cachexia?
- (2013) Kenneth H Fearon LANCET ONCOLOGY
- HMB attenuates muscle loss during sustained energy deficit induced by calorie restriction and endurance exercise
- (2013) Bong-Sup Park et al. METABOLISM-CLINICAL AND EXPERIMENTAL
- JAK/STAT3 pathway inhibition blocks skeletal muscle wasting downstream of IL-6 and in experimental cancer cachexia
- (2012) Andrea Bonetto et al. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
- Constitutive STAT3 Phosphorylation Contributes to Skeletal Muscle Insulin Resistance in Type 2 Diabetes
- (2012) F. Mashili et al. DIABETES
- STAT3 interacts directly with Hsp90
- (2012) Earl Prinsloo et al. IUBMB LIFE
- Myostatin promotes the wasting of human myoblast cultures through promoting ubiquitin-proteasome pathway-mediated loss of sarcomeric proteins
- (2011) Sudarsanareddy Lokireddy et al. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
- Inhibition of FoxO transcriptional activity prevents muscle fiber atrophy during cachexia and induces hypertrophy
- (2011) Sarah A. Reed et al. FASEB JOURNAL
- Definition and classification of cancer cachexia: an international consensus
- (2011) Kenneth Fearon et al. LANCET ONCOLOGY
- HSP90 is essential for Jak-STAT signaling in classical Hodgkin lymphoma cells
- (2009) Nils Schoof et al. Cell Communication and Signaling
- Interleukin-6 and cachexia in ApcMin/+ mice
- (2007) Kristen A. Baltgalvis et al. AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
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