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Pregled bibliografske jedinice broj: 1260708

Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas


Hudolin T, Mengus C, Coulot J, Kastelan Z, El-Saleh A, Spagnoli GC.
Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas // Anticancer Research, 37 (2017), 1375-1380 (međunarodna recenzija, članak, znanstveni)


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Naslov
Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas

Autori
Hudolin T, Mengus C, Coulot J, Kastelan Z, El-Saleh A, Spagnoli GC.

Izvornik
Anticancer Research (0250-7005) 37 (2017); 1375-1380

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Non-muscle-invasive bladder cancer ; indoleamine 2, 3-dioxygenase ; polymerase chain reaction.

Sažetak
Aim: To evaluate indoleamine 2, 3-dioxygenase (IDO) gene expression in non-muscle-invasive urothelial cell bladder carcinoma (NMIBC). Patients and methods: Seventy-four patients undergoing surgical treatment for NMIBC were enrolled in the study. IDO gene expression was assessed by quantitative real-time polymerase chain reaction (qRT-PCR). Results: IDO gene expression was detectable significantly more frequently (48/74, 64.86% vs. 5/21, 23.81%, p<0.001) and to significantly higher extents (p=0.01) in cancer tissues than in normal bladder mucosa. IDO gene expression was observed significantly more frequently in large (p=0.02), high-grade (p=0.05) and stage T1 (p=0.03) than in small, low-grade and stage Ta tumors. Expression levels were also significantly higher in large, high-grade and stage T1 tumors (p<0.01, p=0.05 and p=0.03, respectively). A direct positive correlation between IDO gene expression in tumor tissues and tumor size (R=0.24, p=0.04), grade (R=0.23, p=0.05) and stage (R=0.25, p=0.03) was detected. Multivariate analysis suggested a trend (p=0.08) towards longer overall survival in patients bearing tumors that did not express IDO gene. Conclusion: These data indicate that IDO gene expression is a feature of aggressive NMIBC, suggesting a potential immunosuppressive role of IDO.

Izvorni jezik
Engleski

Znanstvena područja
Temeljne medicinske znanosti



POVEZANOST RADA



Citiraj ovu publikaciju:

Hudolin T, Mengus C, Coulot J, Kastelan Z, El-Saleh A, Spagnoli GC.
Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas // Anticancer Research, 37 (2017), 1375-1380 (međunarodna recenzija, članak, znanstveni)
Hudolin T, Mengus C, Coulot J, Kastelan Z, El-Saleh A, Spagnoli GC. (2017) Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas. Anticancer Research, 37, 1375-1380.
@article{article, year = {2017}, pages = {1375-1380}, keywords = {Non-muscle-invasive bladder cancer, indoleamine 2, 3-dioxygenase, polymerase chain reaction.}, journal = {Anticancer Research}, volume = {37}, issn = {0250-7005}, title = {Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas}, keyword = {Non-muscle-invasive bladder cancer, indoleamine 2, 3-dioxygenase, polymerase chain reaction.} }
@article{article, year = {2017}, pages = {1375-1380}, keywords = {Non-muscle-invasive bladder cancer, indoleamine 2, 3-dioxygenase, polymerase chain reaction.}, journal = {Anticancer Research}, volume = {37}, issn = {0250-7005}, title = {Expression of Indoleamine 2,3-Dioxygenase Gene Is a Feature of Poorly Differentiated Non-muscle- invasive Urothelial Cell Bladder Carcinomas}, keyword = {Non-muscle-invasive bladder cancer, indoleamine 2, 3-dioxygenase, polymerase chain reaction.} }

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus
  • MEDLINE





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