Hu Chunhong, Wang Xue, Pan Yue, Shu Long, Wu Fang
Department of Oncology, The Second Xiangya Hospital of Central South University, Changsha, Hunan 410011, P.R. China.
Department of VIP Medical Services, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, P.R. China.
Oncol Lett. 2021 May;21(5):341. doi: 10.3892/ol.2021.12602. Epub 2021 Mar 2.
The present case study investigated a rare case of quadruple squamous cell carcinoma following allogeneic hematopoietic stem cell transplantation (HSCT) for leukemia. The main aim of the case study was to determine the pathogenesis and provide novel methods for the diagnosis and treatment of similar cases. The presence of genetic mutations in the p53, EGFR, KRAS and BRAF genes were analyzed and the presence of microsatellite instability (MSI) was determined. In addition, the expression levels of the proteins p53 and EGFR were investigated. The results identified a genetic mutation in p53, of which its expression levels were upregulated. In addition, the majority of the tumor tissues presented with MSI. Therefore, the present findings suggested that the genetic mutations in p53 caused by MSI following allogeneic HSCT may promote tumorigenesis. In addition, the expression levels of the EGFR protein were upregulated, leading to an increase in MAPK signaling pathway activation, which may also serve an important role.
本病例研究调查了1例白血病患者接受异基因造血干细胞移植(HSCT)后发生四重鳞状细胞癌的罕见病例。该病例研究的主要目的是确定发病机制,并为类似病例的诊断和治疗提供新方法。分析了p53、表皮生长因子受体(EGFR)、KRAS和BRAF基因中的基因突变情况,并确定了微卫星不稳定性(MSI)的存在。此外,还研究了p53和EGFR蛋白的表达水平。结果发现p53基因发生了突变,其表达水平上调。此外,大多数肿瘤组织表现为MSI。因此,本研究结果表明,异基因HSCT后由MSI引起的p53基因突变可能促进肿瘤发生。此外,EGFR蛋白的表达水平上调,导致丝裂原活化蛋白激酶(MAPK)信号通路激活增加,这也可能起重要作用。