| Online-Ressource |
Verfasst von: | Reinmuth, Niels [VerfasserIn]  |
| Kloos, Sebastian [VerfasserIn]  |
| Warth, Arne [VerfasserIn]  |
| Risch, Angela [VerfasserIn]  |
| Muley, Thomas [VerfasserIn]  |
| Hoffmann, Hans [VerfasserIn]  |
| Thomas, Michael [VerfasserIn]  |
| Meister, Michael [VerfasserIn]  |
Titel: | Insulin-like growth factor 1 pathway mutations and protein expression in resected non-small cell lung cancer |
Verf.angabe: | Niels Reinmuth MD, PhD, Sebastian Kloos, Arne Warth MD, Angela Risch PhD, Thomas Muley PhD, Hans Hoffmann MD, PhD, Michael Thomas MD, PhD, Michael Meister PhD |
E-Jahr: | 2014 |
Jahr: | 30 January 2014 |
Umfang: | 7 S. |
Fussnoten: | Gesehen am 18.08.2020 |
Titel Quelle: | Enthalten in: Human pathology |
Ort Quelle: | New York, NY [u.a.] : Elsevier, 1970 |
Jahr Quelle: | 2014 |
Band/Heft Quelle: | 45(2014), 6, Seite 1162-1168 |
ISSN Quelle: | 1532-8392 |
Abstract: | The purpose of this study was to characterize the prevalence of insulin-like growth factor 1 receptor (IGF1R) mutations, single nucleotide polymorphisms (SNP), and protein overexpression in surgically resected non-small cell lung cancers in relation to patient characteristics and prognosis. This retrospective study was conducted on 304 patients with non-small cell lung cancers who underwent curative pulmonary resection (median follow-up for surviving patients, 3.6 years). IGF1R gene alterations (n = 304) and protein expression (n = 181) were evaluated by polymerase chain reaction-based assays and immunohistochemistry, respectively. Membranous and cytoplasmic staining were analyzed separately. In an exploratory analysis, 1 silent mutation in exon 16 and 3 mutations in introns of the IGF1R gene comprising the tyrosine kinase domain were detected. Moreover, evaluating selected IGF1R SNPs, patients with adenocarcinomas and homozygous for the rs8038415 T-allele had a significantly better survival (P = .025) but no different disease-free survival. Regarding expression, membranous but not cytoplasmic IGF1R staining was higher in squamous cell carcinomas versus other histologies (P < .0001) and showed a trend to longer survival (P = .08). No association between SNP variations and protein expression was found. Membranous IGF1R protein expression is higher in squamous cell versus other histologies but does not correlate with prognosis. SNPs and mutations can be detected and may harbor prognostic value. These alterations may be of interest when evaluating the IGF1R as potential therapeutic target and should receive further research. |
DOI: | doi:10.1016/j.humpath.2014.01.010 |
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.
Volltext ; Verlag: https://doi.org/10.1016/j.humpath.2014.01.010 |
| Volltext: http://www.sciencedirect.com/science/article/pii/S004681771400046X |
| DOI: https://doi.org/10.1016/j.humpath.2014.01.010 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Sach-SW: | Mutation |
| Non-small cell lung cancer |
| Prognosis |
| SNP |
K10plus-PPN: | 1727340965 |
Verknüpfungen: | → Zeitschrift |
Insulin-like growth factor 1 pathway mutations and protein expression in resected non-small cell lung cancer / Reinmuth, Niels [VerfasserIn]; 30 January 2014 (Online-Ressource)