Open Access

Tumor hyperthermia research progress and application prospect in tumoroids (Review)

  • Authors:
    • Wei Mao
    • Wen Li
    • Xuguang Hu
  • View Affiliations

  • Published online on: February 14, 2024     https://doi.org/10.3892/mco.2024.2729
  • Article Number: 31
  • Copyright: © Mao et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Tumor hyperthermia is the fifth tumor treatment method after surgery, chemotherapy, radiotherapy and biological therapy, and is also one of the important adjuvant treatment methods for tumors. Hyperthermia can not only directly eliminate tumor cells, but also stimulate the antitumor immune response of the body, and improve the sensitivity of tumor tissues to radiotherapy and chemotherapy. An organoid is a tissue‑specific cell cluster formed by 3D culture of various types of cells derived from target organ stem cells, which can reproduce the functions of target organs in vivo. At present, the research models of hepatocellular carcinoma (HCC) in vitro are mainly 2D culture cell line models, and there is no clinical report on tumor hyperthermia using HCC tumoroids. It was hypothesized that this will be a promising research direction.
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April-2024
Volume 20 Issue 4

Print ISSN: 2049-9450
Online ISSN:2049-9469

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Copy and paste a formatted citation
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Spandidos Publications style
Mao W, Li W and Hu X: Tumor hyperthermia research progress and application prospect in tumoroids (Review). Mol Clin Oncol 20: 31, 2024.
APA
Mao, W., Li, W., & Hu, X. (2024). Tumor hyperthermia research progress and application prospect in tumoroids (Review). Molecular and Clinical Oncology, 20, 31. https://doi.org/10.3892/mco.2024.2729
MLA
Mao, W., Li, W., Hu, X."Tumor hyperthermia research progress and application prospect in tumoroids (Review)". Molecular and Clinical Oncology 20.4 (2024): 31.
Chicago
Mao, W., Li, W., Hu, X."Tumor hyperthermia research progress and application prospect in tumoroids (Review)". Molecular and Clinical Oncology 20, no. 4 (2024): 31. https://doi.org/10.3892/mco.2024.2729