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A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival

  • Authors:
    • Fang‑Xiao Zhu
    • Xiao‑Tao Wang
    • Hui‑Qiong Zeng
    • Zhi‑Hua Yin
    • Zhi‑Zhong Ye
  • View Affiliations / Copyright

    Affiliations: Department of Rheumatology, Shenzhen Futian Hospital for Rheumatic Diseases, Shenzhen, Guangdong 518040, P.R. China, Department of Hematology, The Second Affiliated Hospital of Guilin Medical College, Guilin, Guangxi 541001, P.R. China
    Copyright: © Zhu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Pages: 5310-5324
    |
    Published online on: September 19, 2019
       https://doi.org/10.3892/ol.2019.10881
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Abstract

Autophagy has an important role in the pathogenesis of plasma cell development and multiple myeloma (MM); however, the prognostic role of autophagy‑related genes (ARGs) in MM remains undefined. In the present study, the expression profiles of 234 ARGs were obtained from a Gene Expression Omnibus dataset (accession GSE24080), which contains 559 samples of patients with MM analyzed with 54,675 probes. Univariate Cox regression analysis identified 55 ARGs that were significantly associated with event‑free survival of MM. Furthermore, a risk score with 16 survival‑associated ARGs was developed using multivariate Cox regression analysis, including ATIC, BNIP3L, CALCOCO2, DNAJB1, DNAJB9, EIF4EBP1, EVA1A, FKBP1B, FOXO1, FOXO3, GABARAP, HIF1A, NCKAP1, PRKAR1A and SUPT20H, was constructed. Using this prognostic signature, patients with MM could be separated into high‑ and low‑risk groups with distinct clinical outcomes. The area under the curve values for the receiver operating characteristic curves were 0.740, 0.741 and 0.712 for 3, 5 and 10 years prognosis predictions, respectively. Notably, the prognostic role of this risk score could be validated with another four independent cohorts (accessions: GSE57317, GSE4581, GSE4452 and GSE4204). In conclusion, ARGs may serve vital roles in the progression of MM, and the ARGs‑based prognostic model may provide novel ideas for clinical applications in MM.
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Copy and paste a formatted citation
Spandidos Publications style
Zhu FX, Wang XT, Zeng HQ, Yin ZH and Ye ZZ: A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival. Oncol Lett 18: 5310-5324, 2019.
APA
Zhu, F., Wang, X., Zeng, H., Yin, Z., & Ye, Z. (2019). A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival. Oncology Letters, 18, 5310-5324. https://doi.org/10.3892/ol.2019.10881
MLA
Zhu, F., Wang, X., Zeng, H., Yin, Z., Ye, Z."A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival". Oncology Letters 18.5 (2019): 5310-5324.
Chicago
Zhu, F., Wang, X., Zeng, H., Yin, Z., Ye, Z."A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival". Oncology Letters 18, no. 5 (2019): 5310-5324. https://doi.org/10.3892/ol.2019.10881
Copy and paste a formatted citation
x
Spandidos Publications style
Zhu FX, Wang XT, Zeng HQ, Yin ZH and Ye ZZ: A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival. Oncol Lett 18: 5310-5324, 2019.
APA
Zhu, F., Wang, X., Zeng, H., Yin, Z., & Ye, Z. (2019). A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival. Oncology Letters, 18, 5310-5324. https://doi.org/10.3892/ol.2019.10881
MLA
Zhu, F., Wang, X., Zeng, H., Yin, Z., Ye, Z."A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival". Oncology Letters 18.5 (2019): 5310-5324.
Chicago
Zhu, F., Wang, X., Zeng, H., Yin, Z., Ye, Z."A predicted risk score based on the expression of 16 autophagy‑related genes for multiple myeloma survival". Oncology Letters 18, no. 5 (2019): 5310-5324. https://doi.org/10.3892/ol.2019.10881
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