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Biomarkers of chondrosarcoma
  1. Wonju Jeong1,
  2. Ha-Jeong Kim2,3
  1. 1 Department of Orthopedic Surgery, Daegu Top Hospital, Daegu, The Republic of Korea
  2. 2 Department of Physiology, School of Medicine, Kyungpook National University, Daegu, The Republic of Korea
  3. 3 BK21 Plus KNU Biomedical Convergence Program, Department of Biomedical Science, School of Medicine, Kyungpook National University, Daegu, The Republic of Korea
  1. Correspondence to Prof Ha-Jeong Kim, Department of Physiology, School of Medicine, Kyungpook National University, Daegu 41944, The Republic of Korea; kimhajeong{at}knu.ac.kr

Abstract

Clinical outcome prediction is major concern to patients with cancer. Various molecular markers in various carcinomas have been identified in the past few decades. However, accurate predictors in chondrosarcoma have not been developed, even though chondrosarcoma is the second most common primary bone tumour. Chondrosarcoma is the cartilage-forming malignancy and shows a wide spectrum of clinicopathological behaviours. The majority of chondrosarcoma grows slowly and rarely metastasises, and adequate surgery leads to a good prognosis. However, wide surgical excision is acquired in high-grade chondrosarcoma, because this tumour is highly resistant to chemotherapy and radiotherapy. To decide best therapy, accurate diagnostic markers are also necessary in chondrosarcoma. It is reported that angiogenesis and lymphangiogenesis increase by chondrosarcoma staging, and they are promoted by leptin and adiponectin. Several microRNAs to regulate vascular endothelial growth factor (VEGF)-A and VEGF-C are also reported. Alpha-methylacyl-CoA racemase and periostin are proposed as new biomarkers for differential diagnosis of enchondroma and chondrosarcoma. This review summarises that chondrosarcoma diagnostic markers are currently reported.

  • bone tumours
  • tumour markers
  • diagnosis

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Footnotes

  • Handling editor Runjan Chetty.

  • Contributors Both authors were involved in the writing of this review paper.

  • Funding This work was supported by Biomedical Research Institute grant, Kyungpook National University Hospital (2014).

  • Competing interests None declared.

  • Patient consent Not required.

  • Provenance and peer review Not commissioned; externally peer reviewed.