1. RNA-binding protein LIN28 is a sensitive marker of pediatric yolk sac tumors
- Author
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Zhongliang Chen, Yulong Tong, Xin-He Lai, Shaoguang Feng, Dazhou Wu, Songsong Huang, Delei Shen, and Xiaoming Chen
- Subjects
Male ,0301 basic medicine ,Pathology ,medicine.medical_specialty ,LIN28 ,03 medical and health sciences ,Testicular Neoplasms ,Pediatric surgery ,Biomarkers, Tumor ,Humans ,Medicine ,Yolk sac ,neoplasms ,Ovarian Neoplasms ,business.industry ,Endodermal Sinus Tumor ,Teratoma ,Infant ,RNA-Binding Proteins ,General Medicine ,medicine.disease ,Immunohistochemistry ,Embryonic stem cell ,Staining ,030104 developmental biology ,medicine.anatomical_structure ,Child, Preschool ,Pediatrics, Perinatology and Child Health ,Biomarker (medicine) ,Female ,Surgery ,alpha-Fetoproteins ,Germ cell tumors ,business - Abstract
RNA-binding protein LIN28 is involved in maintaining the pluripotency of embryonic stem cells. It has been detected in different types of testicular and ovarian germ cell tumors (GCTs), but its status in pediatric YSTs (yolk sac tumors) is still unknown. The aim of this study was to determine the immunohistochemical profile of LIN28 in pediatric YSTs. Immunohistochemistry detection of LIN28 was performed in 22 cases of pediatric YSTs and 10 mature teratomas. The percentage of tumor cells stained was scored as 0, 1+ (1–30 % cells), 2+ (31–60 %), 3+ (61–90 %), and 4+ (>90 %). To compare its sensitive and specificity with alpha-fetoprotein (AFP), we also stained AFP in 22 cases of pediatric YSTs and 10 mature teratomas in children. LIN28 staining was high in all 22 pediatric yolk sac tumor (2+ in 1, 3+ in 1, and 4+ in 20), and weak staining of LIN28 was seen in 1 of 10 mature teratomas (1+), 9 of 10 mature teratomas were negative expression. However, the expression of AFP in pediatric YST was lower compared with Lin28 (- in 1, 1+ in 8, 2+ in 12, and 3+ in 1), and weak expression of AFP was seen in 2 of 10 mature teratomas (1+), 8 of 10 mature teratomas were negative. LIN28 had higher intensity expression than AFP in pediatric YSTs (P
- Published
- 2016