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Review Open Access

Crosstalk of methylation and tamoxifen in breast cancer (Review)

  • Authors:
    • Jin Shen
    • Yan He
    • Shengpeng Li
    • Huimin Chen
  • View Affiliations / Copyright

    Affiliations: Department of Rehabilitation, The Affiliated Zhuzhou Hospital of Xiangya Medical College, Central South University, Zhuzhou, Hunan 412000, P.R. China, Department of Neurology, The Affiliated Zhuzhou Hospital of Xiangya Medical College, Central South University, Zhuzhou, Hunan 412000, P.R. China
    Copyright: © Shen et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 180
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    Published online on: August 9, 2024
       https://doi.org/10.3892/mmr.2024.13304
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Abstract

Tamoxifen is a widely used anti‑estrogen drug in the endocrine therapy of breast cancer (BC). It blocks estrogen signaling by competitively binding to estrogen receptor α (ERα), thereby inhibiting the growth of BC cells. However, with the long‑term application of tamoxifen, a subset of patients with BC have shown resistance to tamoxifen, which leads to low overall survival and progression‑free survival. The molecular mechanism of resistance is mainly due to downregulation of ERα expression and abnormal activation of the PI3K/AKT/mTOR signaling pathway. Moreover, the downregulation of targeted gene expression mediated by DNA methylation is an important regulatory mode to control protein expression. In the present review, methylation and tamoxifen are briefly introduced, followed by a focus on the effect of methylation on tamoxifen resistance and sensitivity. Finally, the clinical application of methylation for tamoxifen is described, including its use as a prognostic indicator. Finally, it is hypothesized that when methylation is used in combination with tamoxifen, it could recover the resistance of tamoxifen.
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Copy and paste a formatted citation
Spandidos Publications style
Shen J, He Y, Li S and Chen H: Crosstalk of methylation and tamoxifen in breast cancer (Review). Mol Med Rep 30: 180, 2024.
APA
Shen, J., He, Y., Li, S., & Chen, H. (2024). Crosstalk of methylation and tamoxifen in breast cancer (Review). Molecular Medicine Reports, 30, 180. https://doi.org/10.3892/mmr.2024.13304
MLA
Shen, J., He, Y., Li, S., Chen, H."Crosstalk of methylation and tamoxifen in breast cancer (Review)". Molecular Medicine Reports 30.4 (2024): 180.
Chicago
Shen, J., He, Y., Li, S., Chen, H."Crosstalk of methylation and tamoxifen in breast cancer (Review)". Molecular Medicine Reports 30, no. 4 (2024): 180. https://doi.org/10.3892/mmr.2024.13304
Copy and paste a formatted citation
x
Spandidos Publications style
Shen J, He Y, Li S and Chen H: Crosstalk of methylation and tamoxifen in breast cancer (Review). Mol Med Rep 30: 180, 2024.
APA
Shen, J., He, Y., Li, S., & Chen, H. (2024). Crosstalk of methylation and tamoxifen in breast cancer (Review). Molecular Medicine Reports, 30, 180. https://doi.org/10.3892/mmr.2024.13304
MLA
Shen, J., He, Y., Li, S., Chen, H."Crosstalk of methylation and tamoxifen in breast cancer (Review)". Molecular Medicine Reports 30.4 (2024): 180.
Chicago
Shen, J., He, Y., Li, S., Chen, H."Crosstalk of methylation and tamoxifen in breast cancer (Review)". Molecular Medicine Reports 30, no. 4 (2024): 180. https://doi.org/10.3892/mmr.2024.13304
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