Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Fellhofer-Hofer, Johanna [VerfasserIn]   i
 Franz, Clemens [VerfasserIn]   i
 Vey, Johannes [VerfasserIn]   i
 Kahlert, Christoph [VerfasserIn]   i
 Kalkum, Eva [VerfasserIn]   i
 Mehrabi, Arianeb [VerfasserIn]   i
 Halama, Niels [VerfasserIn]   i
 Probst, Pascal [VerfasserIn]   i
 Klupp, Fee [VerfasserIn]   i
Titel:Chemokines as prognostic factor in colorectal cancer patients
Titelzusatz:a systematic review and meta-analysis
Verf.angabe:Johanna Fellhofer-Hofer, Clemens Franz, Johannes A. Vey, Christoph Kahlert, Eva Kalkum, Arianeb Mehrabi, Niels Halama, Pascal Probst and Fee Klupp
E-Jahr:2024
Jahr:15 May 2024
Umfang:14 S.
Illustrationen:Illustrationen
Fussnoten:Gesehen am 11.06.2025
Titel Quelle:Enthalten in: International journal of molecular sciences
Ort Quelle:Basel : Molecular Diversity Preservation International, 2000
Jahr Quelle:2024
Band/Heft Quelle:25(2024), 10, Artikel-ID 5374, Seite 1-14
ISSN Quelle:1422-0067
 1661-6596
Abstract:Chemokines orchestrate many aspects of tumorigenic processes such as angiogenesis, apoptosis and metastatic spread, and related receptors are expressed on tumor cells as well as on inflammatory cells (e.g., tumor-infiltrating T cells, TILs) in the tumor microenvironment. Expressional changes of chemokines and their receptors in solid cancers are common and well known, especially in affecting colorectal cancer patient outcomes. Therefore, the aim of this current systematic review and meta-analysis was to classify chemokines as a prognostic biomarker in colorectal cancer patients. A systematic literature search was conducted in PubMed, CENTRAL and Web of Science. Information on the chemokine expression of 25 chemokines in colorectal cancer tissue and survival data of the patients were investigated. The hazard ratio of overall survival and disease-free survival with chemokine expression was examined. The risk of bias was analyzed using Quality in Prognosis Studies. Random effects meta-analysis was performed to determine the impact on overall respectively disease survival. For this purpose, the pooled hazard ratios (HR) and their 95% confidence intervals (CI) were used for calculation. Twenty-five chemokines were included, and the search revealed 5556 publications. A total of thirty-one publications were included in this systematic review and meta-analysis. Overexpression of chemokine receptor CXCR4 was associated with both a significantly reduced overall survival (HR = 2.70, 95%-CI: 1.57 to 4.66, p = 0.0003) as well as disease-free survival (HR = 2.68, 95%-CI: 1.41 to 5.08, p = 0.0026). All other chemokines showed either heterogeneous results or few studies were available. The overall risk of bias for CXCR4 was rated low. At the current level of evidence, this study demonstrates that CXCR4 overexpression in patients with colorectal cancer is associated with a significantly diminished overall as well as disease-free survival. Summed up, this systematic review and meta-analysis reveals CXCR4 as a promising prognostic biomarker. Nevertheless, more evidence is needed to evaluate CXCR4 and its antagonists serving as new therapeutic targets.
DOI:doi:10.3390/ijms25105374
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

kostenfrei: Volltext: https://doi.org/10.3390/ijms25105374
 kostenfrei: Volltext: https://www.mdpi.com/1422-0067/25/10/5374
 DOI: https://doi.org/10.3390/ijms25105374
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Biomarkers, Tumor
 chemokine
 Chemokines
 colorectal cancer
 Colorectal Neoplasms
 CXCR4 expression
 Disease-Free Survival
 Humans
 outcome
 Prognosis
 Receptors, CXCR4
 survival
K10plus-PPN:192795570X
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/69355309   QR-Code
zum Seitenanfang