Department of Pathology, Medical School, University of Thessaly, Larissa, Greece.
Pediatr Blood Cancer. 2013 Oct;60(10):E116-7. doi: 10.1002/pbc.24579. Epub 2013 May 15.
Mismatch DNA repair (MMR) mRNA expression analysis was performed on a biopsy of oral mucosa melanin pigmentation lesion, a hamartomatous polyp and peripheral blood derived from a 12-year-old child with Peutz-Jeghers Syndrome (PJS). We present a deficient MMR system, in a PJS patient, which demonstrated low mRNA levels of hMSH6 and hPMS2 and an increasing MMR deficiency from the non-dysplastic lesion to hamartomatous polyp of PJS with a high risk of cancer.
对一位患有 Peutz-Jeghers 综合征(PJS)的 12 岁儿童的口腔黏膜黑色素沉着病变、错构瘤息肉和外周血进行错配修复(MMR)mRNA 表达分析。我们报告了一位 PJS 患者存在 MMR 系统缺陷,表现为 hMSH6 和 hPMS2 的 mRNA 水平较低,并且 MMR 缺陷从非发育不良病变到 PJS 的错构瘤息肉逐渐增加,具有较高的癌症风险。