Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Cancer cachexia: More than skeletal muscle wasting.
Trends Cancer 4, 849-860 (2018)
Cancer cachexia is a multifactorial condition characterized by body weight loss that negatively affects quality of life and survival of patients with cancer. Despite the clinical relevance, there is currently no defined standard of care to effectively counteract cancer-associated progressive tissue wasting. Skeletal muscle atrophy represents the main manifestation of cancer cachexia. However, cancer cachexia is increasingly seen as a systemic phenomenon affecting and/or influenced by various organs. Here, we describe recent developments elucidating the roles of different tissues as well as tissue crosstalk in this wasting syndrome, including potential links to other cancer-associated morbidities. A more comprehensive understanding of cancer cachexia etiology and heterogeneity may enable the development of intervention strategies to prevent or reverse this devastating condition.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
7.038
1.146
53
81
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Review
Schlagwörter
Acute-phase Response; Adipose Triglyceride Lipase; Gut Barrier Dysfunction; Necrosis-factor-alpha; Pancreatic-cancer; Metabolic Dysfunction; Therapeutic Target; Insulin-resistance; Anorexia-cachexia; Mononuclear-cells
Sprache
englisch
Veröffentlichungsjahr
2018
HGF-Berichtsjahr
2018
ISSN (print) / ISBN
2405-8033
e-ISSN
2405-8025
Zeitschrift
Trends in cancer
Quellenangaben
Band: 4,
Heft: 12,
Seiten: 849-860
Verlag
Elsevier
Verlagsort
Amsterdam
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Diabetes and Cancer (IDC)
POF Topic(s)
90000 - German Center for Diabetes Research
Forschungsfeld(er)
Helmholtz Diabetes Center
PSP-Element(e)
G-501900-253
G-501900-251
G-501900-257
G-501900-251
G-501900-257
WOS ID
WOS:000450815300008
Scopus ID
85055264073
PubMed ID
30470306
Erfassungsdatum
2018-11-03