High Expression of NT5DC2 Is a Negative Prognostic Marker in Pulmonary Adenocarcinoma

Schulze AB, Kuntze A, Schmidt LH, Mohr M, Marra A, Hillejan L, Schulz C, Görlich D, Hartmann W, Bleckmann A, Evers G

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

Via immunohistochemistry (IHC) on tissue micro arrays (TMA) clinical and prognostic impact of p53 co-playing 5′-Nucleotidase Domain-Containing Protein 2 (NT5DC2) protein expression was evaluated in 252 NSCLC patients. Confirmatory, gene expression database. mRNA levels of NT5DC2 were studied in 1925 NSCLC patients. High protein expression of NT5DC2 resulted in reduced median overall survival (OS) of patients with stage I-III adenocarcinoma (ADC) (Log Rank p = 0.026, HR 2.04 (1.08−3.87)), but not in squamous cell carcinoma (SCC) (p = 0.514, HR 0.87 (0.57−1.33)). Findings on OS were reproduced via gene expression analysis in ADC (p < 0.001, HR 1.64 (1.30−2.08)) and SCC (p = 0.217, HR 0.86 (0.68−1.09)). Yet, NT5DC2 mRNA levels were higher in SCC compared to ADC (p < 0.001) and in pN2 tumors compared to pN0/1 tumors (p = 0.001). Likewise, NT5DC2 protein expression associated with high-grade SCC. Moreover, NT5DC2 expression was positively correlated with p53 protein (p = 0.018) and TP53 gene expression (p < 0.001) and its survival effect was p53 dependent. While p53 expression was negatively associated with the presence of CD34+ cancer associated fibroblasts (CAFs), NT5DC2 expression insignificantly tended to higher levels of SMA+ CAFs (p = 0.065).

Details zur Publikation

FachzeitschriftCancers
Jahrgang / Bandnr. / Volume14
Ausgabe / Heftnr. / Issue6
StatusVeröffentlicht
Veröffentlichungsjahr2022 (09.03.2022)
Sprache, in der die Publikation verfasst istEnglisch
DOI10.3390/cancers14061395
Link zum Volltexthttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8946072/
StichwörterCAFs; NSCLC; NT5DC2; TP53; p53.

Autor*innen der Universität Münster

Bleckmann, Annalen
Medizinische Klinik A (Med A)
Evers, Georg
Medizinische Klinik A (Med A)
Görlich, Dennis
Institut für Biometrie und Klinische Forschung (IBKF)
Hartmann, Wolfgang
Gerhard-Domagk-Institut für Pathologie
Kuntze, Anna
Gerhard-Domagk-Institut für Pathologie
Mohr, Michael
Medizinische Klinik A (Med A)
Schulze, Arik Bernard
Medizinische Klinik A (Med A)