Discover oncology · 2025
Application of Mendelian randomization and bioinformatic analysis to construct a prognostic model for thyroid cancer and perform pan-cancer analysis.
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Zhan Zhenrun, Weng Zhiyan, Zheng Ke, Lin Jiebin, Yan Sunjie, Shen Ximei
Аннотация
OBJECTIVE: This study aimed to identify causal effects and potential molecular mechanisms of genes associated with THCA development.
METHODS: Bioinformatic analyses were performed to identify differentially expressed genes (DEGs) associated with THCA. Subsequently, Mendelian randomization (MR) analysis was conducted using large-scale eQTL data and THCA GWAS summary statistics to screen for candidate genes. The intersection of DEGs and MR-derived candidate genes was used to determine DEGs with potential causal associations with thyroid carcinogenesis. Functional enrichment analysis, pathway analysis, and immune cell infiltration profiling were performed. External datasets were used for validation. Additionally, prognostic modeling and pan-cancer analyses of the candidate genes were conducted.
RESULTS: IVW-based MR analysis revealed that elevated expression levels of ALOX15B [OR = 1.647, 95% CI (1.120-2.420), P < 0.05], TIAM1 [OR = 1.270, 95% CI (1.001-1.611), P < 0.05], and TMC6 [OR = 1.250, 95% CI (1.021-1.530), P < 0.05] were associated with an increased risk of THCA. Conversely, elevated expression of JUN [OR = 0.795, 95% CI (0.653-0.967), P < 0.05], PAPSS2 [OR = 0.779, 95% CI (0.608-1.000), P < 0.05], and RAP1GAP [OR = 0.895, 95% CI (0.810-0.989), P < 0.05] was associated with a reduced risk. Gene set enrichment analysis (GSEA) indicated that risk genes were enriched in proliferation- and metastasis-related pathways, such as extracellular matrix (ECM)-receptor interaction and cell adhesion molecules (CAMs). Findings from the training set were further validated experimentally and via external datasets. Additionally, candidate risk genes demonstrated associations with the development and progression of multiple tumor types.
CONCLUSION: This study identified ALOX15B, TIAM1, and TMC6 as potential risk genes and JUN, PAPSS2, and RAP1GAP as protective genes in THCA. These genes may serve as promising biomarkers and therapeutic targets for THCA, offering novel insights into precision oncology.
METHODS: Bioinformatic analyses were performed to identify differentially expressed genes (DEGs) associated with THCA. Subsequently, Mendelian randomization (MR) analysis was conducted using large-scale eQTL data and THCA GWAS summary statistics to screen for candidate genes. The intersection of DEGs and MR-derived candidate genes was used to determine DEGs with potential causal associations with thyroid carcinogenesis. Functional enrichment analysis, pathway analysis, and immune cell infiltration profiling were performed. External datasets were used for validation. Additionally, prognostic modeling and pan-cancer analyses of the candidate genes were conducted.
RESULTS: IVW-based MR analysis revealed that elevated expression levels of ALOX15B [OR = 1.647, 95% CI (1.120-2.420), P < 0.05], TIAM1 [OR = 1.270, 95% CI (1.001-1.611), P < 0.05], and TMC6 [OR = 1.250, 95% CI (1.021-1.530), P < 0.05] were associated with an increased risk of THCA. Conversely, elevated expression of JUN [OR = 0.795, 95% CI (0.653-0.967), P < 0.05], PAPSS2 [OR = 0.779, 95% CI (0.608-1.000), P < 0.05], and RAP1GAP [OR = 0.895, 95% CI (0.810-0.989), P < 0.05] was associated with a reduced risk. Gene set enrichment analysis (GSEA) indicated that risk genes were enriched in proliferation- and metastasis-related pathways, such as extracellular matrix (ECM)-receptor interaction and cell adhesion molecules (CAMs). Findings from the training set were further validated experimentally and via external datasets. Additionally, candidate risk genes demonstrated associations with the development and progression of multiple tumor types.
CONCLUSION: This study identified ALOX15B, TIAM1, and TMC6 as potential risk genes and JUN, PAPSS2, and RAP1GAP as protective genes in THCA. These genes may serve as promising biomarkers and therapeutic targets for THCA, offering novel insights into precision oncology.