Correlation of Clinicopathological Parameters with HGF, C-Met, EGFR, and IGF-1R Expression in Uveal Melanoma
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This study evaluated the expression profile of hepatocyte growth factor (HGF), c-Met, epidermal growth factor receptor (EGFR), insulin-like growth factor-1 receptor (IGF-1R), and vitreal and serum EGF, HGF, IGF-1 levels in patients with uveal melanoma and assessed their correlation with the clinicopathological parameters. Forty patients with uveal melanoma were included in the study. Clinicopathological parameters were evaluated with hematoxylin-eosin staining. HGF, c-Met, EGFR, and IGF-1R expressions were evaluated immunohistochemically. HGF, EGF, and IGF-1 levels were measured with enzyme-linked immunosorbent assay in vitreous and serum specimens taken at enucleation and 6 months after the enucleation. HGF, c-Met, IGF-1R, and EGFR expressions were detected in 57.5, 20, 20, and 12.5% of cases, respectively. IGF-1R expression was significantly correlated with the degree of pigmentation, necrosis, and lymphocyte infiltration (P=0.013, 0.04, and 0.017). EGFR expression was significantly correlated with the mitosis rate (P=0.02). Vitreal EGF and serum IGF-1 levels were significantly higher in patients with scleral invasion (15.72+/-29.13, 199.01+/-154.01 pg/ml, respectively) when compared with the patients without invasion (0.56+/-1.05, 33.01+/-36.52 pg/ml) (P=0.03 and 0.015). When the preoperative and postoperative serum growth factor levels were compared, the serum EGF level was found to be lower (125.93+/-62.84, 100.02+/-31.19 pg/ml, P=0.007) and the serum IGF-1 level (165.81+/-153.6, 301.35+/-131.24 pg/ml, P<0.001) was found to be higher in the postoperative 6-month specimens. Uveal melanomas express HGF, c-Met, EGFR, and IGF-1R. Vitreal growth factor levels and expression of EGFR and IGF-1R are correlated with some clinicopathological parameters. IGF-1 and EGF may have a role in the development and progression of uveal melanoma.
Zhao A, Wang Y, Wang Z, Shao Q, Gong Q, Zhu H Oncol Res. 2024; 32(5):983-998.
PMID: 38686044 PMC: 11055987. DOI: 10.32604/or.2024.045972.
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Shu W, Wang J, Zhu X, Wang K, Cherepanoff S, Conway R J Cancer. 2023; 14(18):3477-3495.
PMID: 38021158 PMC: 10647189. DOI: 10.7150/jca.88446.
Chattopadhyay C, Bhattacharya R, Roszik J, Khan F, Wells G, Villanueva H Cancers (Basel). 2022; 14(24).
PMID: 36551732 PMC: 9777326. DOI: 10.3390/cancers14246247.
Lei X, Zhang Y, Mao L, Jiang P, Huang Y, Gu J Front Oncol. 2022; 12:819051.
PMID: 36212475 PMC: 9538722. DOI: 10.3389/fonc.2022.819051.
Gu L, Ma G, Li C, Lin J, Zhao G Front Oncol. 2022; 12:958170.
PMID: 36003786 PMC: 9393514. DOI: 10.3389/fonc.2022.958170.