Alterations in Plasma Lipid Profile before and after Surgical Removal of Soft Tissue Sarcoma

Author:

Lee Jae-Hwa12ORCID,Gwon Mi-Ri13ORCID,Kim Jeung-Il4,Hwang Seung-young5,Seong Sook-Jin1236,Yoon Young-Ran1236,Kim Myungsoo7,Kim Hyojeong8ORCID

Affiliation:

1. Department of Molecular Medicine, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea

2. BK21 FOUR KNU Convergence Educational Program of Biomedical Sciences for Creative Future Talents, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea

3. Clinical Omics Institute, School of Medicine, Kyungpook National University, Daegu 41405, Republic of Korea

4. Department of Orthopaedic Surgery and Biomedical Research Institute, School of Medicine, Pusan National University, Busan 49241, Republic of Korea

5. Pharmacokinetics Laboratory, Clinical Trial Center, Pusan National University Hospital, Busan 49241, Republic of Korea

6. Department of Clinical Pharmacology and Therapeutics, Kyungpook National University Hospital, Daegu 41944, Republic of Korea

7. Department of Neurosurgery, School of Medicine, Kyungpook National University, Daegu 41944, Republic of Korea

8. Department of Internal Medicine, Division of Hemato-Oncology, Maryknoll Hospital, Busan 48972, Republic of Korea

Abstract

Soft tissue sarcoma (STS) is a relatively rare malignancy, accounting for about 1% of all adult cancers. It is known to have more than 70 subtypes. Its rarity, coupled with its various subtypes, makes early diagnosis challenging. The current standard treatment for STS is surgical removal. To identify the prognosis and pathophysiology of STS, we conducted untargeted metabolic profiling on pre-operative and post-operative plasma samples from 24 STS patients who underwent surgical tumor removal. Profiling was conducted using ultra-high-performance liquid chromatography–quadrupole time-of-flight/mass spectrometry. Thirty-nine putative metabolites, including phospholipids and acyl-carnitines were identified, indicating changes in lipid metabolism. Phospholipids exhibited an increase in the post-operative samples, while acyl-carnitines showed a decrease. Notably, the levels of pre-operative lysophosphatidylcholine (LPC) O-18:0 and LPC O-16:2 were significantly lower in patients who experienced recurrence after surgery compared to those who did not. Metabolic profiling may identify aggressive tumors that are susceptible to lipid synthase inhibitors. We believe that these findings could contribute to the elucidation of the pathophysiology of STS and the development of further metabolic studies in this rare malignancy.

Funder

Pusan National University Hospital

Publisher

MDPI AG

Reference45 articles.

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