Abstract 5887: <i>NALCN</i> promoter methylation as a biomarker for metastatic risk in a cohort of non-small cell lung cancer patients

Liquid biopsy enables real-time monitoring of tumor development and response to therapy through the analysis of CTCs and ctDNA. NALCN is a sodium leak channel that is frequently involved in tumor evolution and immunity and acts as a tumor suppressor. Deletion of NALCN has been shown to increase cancer metastasis and the number of CTCs in peripheral blood. In this study, we investigated for the first time NALCN promoter methylation in (a) Aza-treated cell lines (A549, TE671, BT20, and MDA-MB-468), (b) paired NSCLC tissues (n = 22), and (c) plasma cell-free DNA (ctDNA) from patients with NSCLC (early stage n = 39, metastatic n = 39) and DNA from 10 healthy donors (HD) using a newly developed highly specific and sensitive real-time MSP method. Treatment with 5′-aza-dC induced the expression of NALCN only in the A549 cell line, suggesting that DNA methylation regulates its expression in certain cancers. The mRNA expression levels of NALCN were quantified in non-small cell lung cancer (NSCLC) and adjacent non-cancerous tissues, and it was found to be underexpressed in 54.5% of tumor tissues, with significantly higher expression in recurrence-free patients (p = 0.009) than in patients who relapsed. The NALCN methylation level was not statistically significantly correlated with the corresponding expression (p = 0.439), while Kaplan-Meier analysis showed an association between NALCN promoter hypermethylation and worse disease-free intervals (DFIs) (p = 0.017). Evaluation of NALCN methylation in ctDNA revealed that it was detected in 5.1% of early and 10.2% of advanced cases. Our results strongly suggest that epigenetic inactivation of NALCN may predict metastasis in NSCLC. Our results should be validated in further studies based on a larger patient cohort to investigate whether DNA methylation of the NALCN promoter could serve as a potential prognostic DNA methylation biomarker and predictor of metastasis in NSCLC. Citation Format: Eleni Thanou, Dora Londra, Ioanna Balgouranidou, Eleni Eftimiadou, Alexandra Delipetrou, Emilia Tsaroucha, Vasilis Georgoulias, Athanasios Kotsakis, Evi Lianidou, Athina N. Markou. NALCN promoter methylation as a biomarker for metastatic risk in a cohort of non-small cell lung cancer patients [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5887.

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Cancer Research
Published
2025-04-21
DOI
https://doi.org/10.1158/1538-7445.am2025-5887
Primary Topic
MicroRNA in disease regulation
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article
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article

Abstract 5887: NALCN promoter methylation as a biomarker for metastatic risk in a cohort of non-small cell lung cancer patients

Vasilis Georgoulias, Dora Londra, Ioanna Balgkouranidou, Evi Lianidou et al.
Cancer Research
MicroRNA in disease regulation
article

Abstract 5887: NALCN promoter methylation as a biomarker for metastatic risk in a cohort of non-small cell lung cancer patients

Vasilis Georgoulias, Dora Londra, Ioanna Balgkouranidou, Evi Lianidou, Αthanasios Kotsakis, Eleni Thanou, Athina Markou, Emilia Tsaroucha, Alexandra Delipetrou, Eleni Eftimiadou
article en

Abstract

Liquid biopsy enables real-time monitoring of tumor development and response to therapy through the analysis of CTCs and ctDNA. NALCN is a sodium leak channel that is frequently involved in tumor evolution and immunity and acts as a tumor suppressor. Deletion of NALCN has been shown to increase cancer metastasis and the number of CTCs in peripheral blood. In this study, we investigated for the first time NALCN promoter methylation in (a) Aza-treated cell lines (A549, TE671, BT20, and MDA-MB-468), (b) paired NSCLC tissues (n = 22), and (c) plasma cell-free DNA (ctDNA) from patients with NSCLC (early stage n = 39, metastatic n = 39) and DNA from 10 healthy donors (HD) using a newly developed highly specific and sensitive real-time MSP method. Treatment with 5′-aza-dC induced the expression of NALCN only in the A549 cell line, suggesting that DNA methylation regulates its expression in certain cancers. The mRNA expression levels of NALCN were quantified in non-small cell lung cancer (NSCLC) and adjacent non-cancerous tissues, and it was found to be underexpressed in 54.5% of tumor tissues, with significantly higher expression in recurrence-free patients (p = 0.009) than in patients who relapsed. The NALCN methylation level was not statistically significantly correlated with the corresponding expression (p = 0.439), while Kaplan-Meier analysis showed an association between NALCN promoter hypermethylation and worse disease-free intervals (DFIs) (p = 0.017). Evaluation of NALCN methylation in ctDNA revealed that it was detected in 5.1% of early and 10.2% of advanced cases. Our results strongly suggest that epigenetic inactivation of NALCN may predict metastasis in NSCLC. Our results should be validated in further studies based on a larger patient cohort to investigate whether DNA methylation of the NALCN promoter could serve as a potential prognostic DNA methylation biomarker and predictor of metastasis in NSCLC. Citation Format: Eleni Thanou, Dora Londra, Ioanna Balgouranidou, Eleni Eftimiadou, Alexandra Delipetrou, Emilia Tsaroucha, Vasilis Georgoulias, Athanasios Kotsakis, Evi Lianidou, Athina N. Markou. NALCN promoter methylation as a biomarker for metastatic risk in a cohort of non-small cell lung cancer patients [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 1 (Regular Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_1):Abstract nr 5887.

Cancer ResearchVol. 85(8_Supplement_1)
Democritus University of Thrace (GR), National and Kapodistrian University of Athens (GR), Sotiria General Hospital (GR)
Openalex Percentile: Top 90%
MicroRNA in disease regulation
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