Correlation of PD-L1 and HIF-1 Alpha Expression with KRAS Mutation and Clinicopathological Parameters in Non-Small Cell Lung Cancer

被引:0
|
作者
Ozilhan, Seda Er [1 ]
Efil, Safa Can [2 ]
Canakci, Dogukan [3 ]
Agackiran, Yetkin [4 ]
Dede, Didem Sener [5 ]
Kandemir, Nilufer Onak [1 ]
Dogan, Mehmet [6 ]
Unal, Tuba Dilay Kokenek [6 ]
Kiran, Merve Meryem [1 ]
Kayacetin, Serra [7 ]
Balta, Hilal [7 ]
Dogan, Hayriye Tatli [6 ]
机构
[1] Ankara Bilkent City Hosp, Dept Pathol, TR-06800 Ankara, Turkiye
[2] Ankara Bilkent City Hosp, Dept Med Oncol, TR-06800 Ankara, Turkiye
[3] Ankara Yildirim Beyazit Univ, Fac Med, TR-06800 Ankara, Turkiye
[4] Hlth Sci Univ, Ankara Ataturk Sanatoryum Hosp, Dept Pathol, TR-06290 Ankara, Turkiye
[5] Ankara Yildirim Beyazit Univ, Fac Med, Dept Med Oncol, TR-06800 Ankara, Turkiye
[6] Ankara Yildirim Beyazit Univ, Fac Med, Dept Pathol, TR-06800 Ankara, Turkiye
[7] Hlth Sci Univ, Ankara Bilkent City Hosp, Dept Pathol, TR-06290 Ankara, Turkiye
关键词
HIF-1; alpha; KRAS; lung cancer; PD-L1; IMMUNOTHERAPY; HIF-1-ALPHA; SAFETY;
D O I
10.3390/cimb47020121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Lung cancer remains the leading cause of cancer-related deaths worldwide, with non-small cell lung carcinomas (NSCLCs) comprising the majority of cases. Among the common driver mutations, KRAS plays a critical role in guiding treatment strategies. This study evaluates the expression of programmed death-ligand 1 (PD-L1) and hypoxia-inducible factor 1-alpha (HIF-1 alpha) in KRAS-mutant NSCLCs and investigates their associations with clinicopathological findings. Methods: A total of 85 cases with KRAS mutations were analyzed. Immunohistochemical staining for HIF-1 alpha and PD-L1 was performed, and their relationships with mutation status and prognostic variables were assessed. Results: A significant correlation was identified between HIF-1 alpha expression and PD-L1 expression in tumor cells. While the KRAS G12C mutation was not significantly associated with HIF-1 alpha expression in tumor cells, it demonstrated a notable relationship with HIF-1 alpha expression in the tumor microenvironment and PD-L1 expression. However, PD-L1 and HIF-1 alpha expression did not significantly influence overall survival outcomes. Conclusions: Expression of PD-L1 was positively correlated with HIF-1 alpha, which may provide evidence for a novel therapy targeting PD-L1 and HIF-1 alpha in NSCLC. Further comprehensive studies are warranted to elucidate the prognostic implications of tumor-microenvironment and mutation interactions.
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页数:13
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