GGT6 as a Prognostic Biomarker and Therapeutic Target in Melanoma Using an Information-theoretical Method.

IF 2.6 4区 医学 Q2 GENETICS & HEREDITY
Yi-Fei Yang, Yun Geng, Hui Xu, Kazunori Akimoto, Yun-Wen Zheng, Yuyun Xiong, Yu-Mei Li
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引用次数: 0

Abstract

Background/aim: Melanoma is an aggressive malignancy with rising global incidence. While early surgical intervention improves survival in localized cases, treatment resistance and recurrence remain a challenge. This underscores the critical need to identify prognostic biomarkers for early diagnosis, personalized treatment, and novel therapeutic development.

Materials and methods: The GSE126076 and melanoma dataset (Skin Cutaneous Melanoma, TCGA, PanCancer Atlas) were analyzed using an information-theoretical method to identify prognostic factors. Survival analysis was performed via Kaplan-Meier curves and log-rank tests to compare high- and low-mRNA expression groups. In vitro, A375 cells and A2058 cells were treated with the GGT inhibitor 6-diazo-5-oxo-L-norleucin (DON). Cell viability was assessed using the CCK-8 assay and intracellular GSH levels were measured following treatment.

Results: Through information-theoretic analysis and survival analysis, we identified GGT6 as a prognostic gene in melanoma. Survival analysis revealed that high GGT6 expression was significantly associated with shorter disease-specific survival across all disease stages. In vitro, 10 μM DON for 72 h reduced A375 cell proliferation by 90.72% versus control (p<0.0001), with an IC50 of 5.14 μM; and reduced A2058 cell proliferation by 60.93% (p<0.0001), with an IC50 of 7.93 μM. Measurement of GSH levels of A375 and A2058 cells revealed that melanoma cells treated with 10 μM DON exhibited lower GSH levels compared with the respective control groups (p<0.0001 and p=0.0042, respectively).

Conclusion: Our study is the first to demonstrate the association between GGT6 expression levels and melanoma prognosis, and reveals that GGT inhibition suppresses melanoma cell viability. These findings provide new insights into the mechanisms of melanoma development and progression, and suggest GGT as a potential therapeutic target for clinical treatment.

GGT6作为黑色素瘤预后生物标志物和治疗靶点的信息理论研究
背景/目的:黑色素瘤是一种侵袭性恶性肿瘤,全球发病率不断上升。虽然早期手术干预提高了局部病例的生存率,但治疗抵抗和复发仍然是一个挑战。这强调了识别预后生物标志物以进行早期诊断、个性化治疗和新疗法开发的迫切需要。材料和方法:采用信息论方法分析GSE126076和黑色素瘤数据集(Skin - Skin melanoma, TCGA, PanCancer Atlas),以确定预后因素。通过Kaplan-Meier曲线和log-rank检验进行生存分析,比较mrna高表达组和低表达组。体外用GGT抑制剂6-重氮-5-氧- l -去甲亮素(DON)处理A375细胞和A2058细胞。使用CCK-8法评估细胞活力,并在治疗后测量细胞内GSH水平。结果:通过信息论分析和生存分析,我们确定了GGT6是黑色素瘤的预后基因。生存分析显示,在所有疾病阶段,高GGT6表达与较短的疾病特异性生存显著相关。体外10 μM DON作用72 h, A375细胞增殖能力较对照组降低90.72% (p50为5.14 μM), A2058细胞增殖能力降低60.93% (p50为7.93 μM)。测量A375和A2058细胞的GSH水平显示,与各自的对照组相比,10 μM DON处理的黑色素瘤细胞的GSH水平较低(pp=0.0042)。结论:我们的研究首次证实了GGT6表达水平与黑色素瘤预后之间的相关性,并揭示了GGT抑制抑制黑色素瘤细胞活力。这些发现为黑色素瘤的发生和发展机制提供了新的见解,并建议GGT作为临床治疗的潜在治疗靶点。
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来源期刊
Cancer Genomics & Proteomics
Cancer Genomics & Proteomics ONCOLOGY-GENETICS & HEREDITY
CiteScore
5.00
自引率
8.00%
发文量
51
期刊介绍: Cancer Genomics & Proteomics (CGP) is an international peer-reviewed journal designed to publish rapidly high quality articles and reviews on the application of genomic and proteomic technology to basic, experimental and clinical cancer research. In this site you may find information concerning the editorial board, editorial policy, issue contents, subscriptions, submission of manuscripts and advertising. The first issue of CGP circulated in January 2004. Cancer Genomics & Proteomics is a journal of the International Institute of Anticancer Research. From January 2013 CGP is converted to an online-only open access journal. Cancer Genomics & Proteomics supports (a) the aims and the research projects of the INTERNATIONAL INSTITUTE OF ANTICANCER RESEARCH and (b) the organization of the INTERNATIONAL CONFERENCES OF ANTICANCER RESEARCH.
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