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Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver

  • Authors:
    • Meng Lian
    • Hongbao Cao
    • Ancha Baranova
    • Kamil Can Kural
    • Lizhen Hou
    • Shizhi He
    • Qing Shao
    • Jugao Fang
  • View Affiliations / Copyright

    Affiliations: Department of Otorhinolaryngology Head and Neck Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, P.R. China, Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan, Shanxi 030001, P.R. China, School of Systems Biology, George Mason University, Fairfax, VA 22030, USA, Department of Breast and Thyroid Surgery, Jiangyin People's Hospital, Jiangyin, Jiangsu 214400, P.R. China
    Copyright: © Lian et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 3634-3642
    |
    Published online on: April 10, 2020
       https://doi.org/10.3892/ol.2020.11530
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Abstract

The prevalence of thyroid cancer (TC) is high in the elderly. The present study was based on the hypothesis that genes, which have increased activity with aging, may play a role in the development of TC. A large‑scale literature‑based data analysis was conducted to explore the genes that are implicated in both TC and aging. Subsequently, a mega‑analysis of 16 RNA expression datasets (1,222 samples: 439 healthy controls, and 783 patients with TC) was conducted to test a set of genes associated with aging but not TC. To uncover a possible link between these genes and TC, a functional pathway analysis was conducted, and the results were validated by analysis of gene co‑expression. A multiple linear regression (MLR) model was employed to study the possible influence of sample size, population region and study age on the gene expression levels in TC. A total of 262 and 816 genes were identified to have increased activity with aging and TC, respectively; with a significant overlap of 63 genes (P<3.82x10‑35). The mega‑analysis revealed two aging‑associated genes (CHI3L1 and TNFRSF12A) to be significantly associated with TC (P<2.05x10‑8), and identified the association with multiple hypoxia‑driven pathways through functional pathway analysis, also confirmed by the co‑expression analysis. The MLR analysis identified population region as a significant factor contributing to the expression levels of CHI3L1 and TNFRSF12A in TC samples (P<3.24x10‑4). The determination of genes that promote aging was warranted due to their possible involvement in TC. The present study suggests CHI3L1 and TNFRSF12A as novel common risk genes associated with both aging and TC.
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Copy and paste a formatted citation
Spandidos Publications style
Lian M, Cao H, Baranova A, Kural KC, Hou L, He S, Shao Q and Fang J: Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver. Oncol Lett 19: 3634-3642, 2020.
APA
Lian, M., Cao, H., Baranova, A., Kural, K.C., Hou, L., He, S. ... Fang, J. (2020). Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver. Oncology Letters, 19, 3634-3642. https://doi.org/10.3892/ol.2020.11530
MLA
Lian, M., Cao, H., Baranova, A., Kural, K. C., Hou, L., He, S., Shao, Q., Fang, J."Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver". Oncology Letters 19.6 (2020): 3634-3642.
Chicago
Lian, M., Cao, H., Baranova, A., Kural, K. C., Hou, L., He, S., Shao, Q., Fang, J."Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver". Oncology Letters 19, no. 6 (2020): 3634-3642. https://doi.org/10.3892/ol.2020.11530
Copy and paste a formatted citation
x
Spandidos Publications style
Lian M, Cao H, Baranova A, Kural KC, Hou L, He S, Shao Q and Fang J: Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver. Oncol Lett 19: 3634-3642, 2020.
APA
Lian, M., Cao, H., Baranova, A., Kural, K.C., Hou, L., He, S. ... Fang, J. (2020). Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver. Oncology Letters, 19, 3634-3642. https://doi.org/10.3892/ol.2020.11530
MLA
Lian, M., Cao, H., Baranova, A., Kural, K. C., Hou, L., He, S., Shao, Q., Fang, J."Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver". Oncology Letters 19.6 (2020): 3634-3642.
Chicago
Lian, M., Cao, H., Baranova, A., Kural, K. C., Hou, L., He, S., Shao, Q., Fang, J."Aging‑associated genes TNFRSF12A and CHI3L1 contribute to thyroid cancer: An evidence for the involvement of hypoxia as a driver". Oncology Letters 19, no. 6 (2020): 3634-3642. https://doi.org/10.3892/ol.2020.11530
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