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Advances in drug resistance of osteosarcoma caused by pregnane X receptor.
Mao, Kunhong; Liu, Can; Tang, Zhongwen; Rao, Zhouzhou; Wen, Jie.
Affiliation
  • Mao K; Key Laboratory of Translational Cancer Stem Cell Research, Department of Physiology, Hunan Normal University School of Medicine, Changsha, China.
  • Liu C; Department of Anatomy, Hunan Normal University school of Medicine, Changsha, China.
  • Tang Z; Department of Pediatric Orthopedics, Hunan Provincial People's Hospital, The First Affiliated Hospital of Hunan Normal University, Changsha, China.
  • Rao Z; Key Laboratory of Translational Cancer Stem Cell Research, Department of Physiology, Hunan Normal University School of Medicine, Changsha, China.
  • Wen J; Department of Anatomy, Hunan Normal University school of Medicine, Changsha, China.
Drug Metab Rev ; : 1-14, 2024 Jun 13.
Article in En | MEDLINE | ID: mdl-38872275
ABSTRACT
Osteosarcoma (OS) is a prevalent malignancy among adolescents, commonly manifesting during childhood and adolescence. It exhibits a high degree of malignancy, propensity for metastasis, rapid progression, and poses challenges in clinical management. Chemotherapy represents an efficacious therapeutic modality for OS treatment. However, chemotherapy resistance of OS is a major problem in clinical treatment. In order to treat OS effectively, it is particularly important to explore the mechanism of chemotherapy resistance in OS.The Pregnane X receptor (PXR) is a nuclear receptor primarily involved in the metabolism, transport, and elimination of xenobiotics, including chemotherapeutic agents. PXR involves three stages of drug metabolism stage I drug metabolism enzymes; stage II drug binding enzyme; stage III drug transporter.PXR has been confirmed to be involved in the process of chemotherapy resistance in malignant tumors. The expression of PXR is increased in OS, which may be related to drug resistance of OS. Therefore, wereviewed in detail the role of PXR in chemotherapy drug resistance in OS.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Drug Metab Rev Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Drug Metab Rev Year: 2024 Document type: Article Affiliation country: China Country of publication: United kingdom