Abstract

It has been reported that phospholipase D1 (PLD1) - a key enzyme involved in lipid metabolism - is important for the initiation and progression of various human solid cancers; however, its biological significance and regulation in human osteosarcomas remain elusive. In this study, We found that PLD1 and Specificity Protein 1 (Sp1) expression were elevated in 137 osteosarcoma specimens with immunohistochemical staining. Our results showed that both PLD1 and Sp1 were expressed at much higher rates in the cancerous tissue compared to adjacent normal tissue. A correlation analyze also indicated that PLD1 was significantly associated with lactate dehydrogenase expression (p = 0.041) and the Enneking stage (p = 0.000), while Sp1 was significantly associated with the nuclear grade (p = 0.024). Furthermore, survival analyses showed that elevated PLD1 confers a poor prognosis on patients with osteosarcomas, acting as an independent prognostic factor. Of note, we showed a positive correlation between PLD1 and Sp1 expression in the cancer tissues (r = 0.357; p < 0.001). High co-expression of the two molecules results in the worst prognosis for the patients, and can also be regarded as independent prognostic factor (p = 0.001; HR = 2.71; 95% CI 1.53–4.80).

Highlights

  • As the most common primary malignant bone tumor in children and adolescents, osteosarcomas arise most frequently in the metaphysis of long bones [1]

  • We examined the expression and prognostic significance of phospholipase D1 (PLD1) - a critical enzyme involved in lipid metabolism - in osteosarcomas

  • Our results showed that PLD1 was elevated in the disease associated with a poor prognosis

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Summary

Introduction

As the most common primary malignant bone tumor in children and adolescents, osteosarcomas arise most frequently in the metaphysis of long bones [1]. A growing body of research has shown that abnormal lipid metabolism is involved in the development of many types of cancer [5]. The classic isoform of PLD, PLD1, is highly expressed in various human tumors, including in breast [6] and gastric cancer [7], and was stated to play a critical role in tumor progression [8]. Despite these advancements, little was known about its expression or biological significance in human osteosarcomas

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