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Cited 5 time in webofscience Cited 5 time in scopus
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Fc Receptor Expression as a Prognostic Factor in Patients With Non-small-cell Lung Canceropen access

Authors
Kim, Min HyeLee, Jeong HeeLee, Jong SilKim, Dong ChulYang, Jung WookAn, Hyo JungNa, Ji MinShin, Meong CheolSong, Dae Hyun
Issue Date
Nov-2022
Publisher
International Institute of Anticancer Research
Keywords
Fc receptor; non-small-cell lung cancer; survival analysis; prognosis; lung cancer prognosis
Citation
In Vivo, v.36, no.6, pp 2708 - 2713
Pages
6
Indexed
SCIE
SCOPUS
Journal Title
In Vivo
Volume
36
Number
6
Start Page
2708
End Page
2713
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/29591
DOI
10.21873/invivo.13006
ISSN
0258-851X
1791-7549
Abstract
Background/Aim: The neonatal Fc receptor (FcRn) is a major histocompatibility class I-like molecule responsible for the transfer of passive humoral immunity from a mother to her newborn. Recent research revealed that FcRn is involved in antigen-presentation, humoral immunity and antitumor immunity of various types of cancer, such as lung, colon and breast. Lung cancer is the leading cause of cancer -related death and non-small cell lung cancer (NSCLC) accounts for 85% of all lung cancer. NSCLC is a highly heterogeneous disease and this affects the prognosis. Therefore, many studies have tried to identify factors that are associated with prognosis. The lungs are a major organ expressing FcRn. We aimed to evaluate FcRn expression in surgical specimens of NSCLC and determine its correlation with patient prognosis. Materials and Methods: We analyzed 140 NSCLC surgical specimens for FcRn expression using immunohistochemistry and correlated positivity with clinicopathology and survival of these patients. A chi-squared test and Kaplan-Meier analysis with log-rank tests were performed for statistical evaluation. Results: The FcRn-positive group had a significantly higher disease-free survival and a tendency towards increased disease-specific survival in patients with tumor-node-metastasis stage I NSCLC. Conclusion: Our study supports the hypothesis that FcRn down-regulation is associated with NSCLC progression.
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