Department of Otorhinolaryngology, Head and Neck Surgery, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
Eur Arch Otorhinolaryngol. 2011 Nov;268(11):1639-46. doi: 10.1007/s00405-011-1529-7. Epub 2011 Feb 18.
The aim of this retrospective analysis was to evaluate the status of p53 and possible mutations in Merkel cell carcinoma (MCC) cell lines and MCC tissue samples. The p53 mutations are common in different cancer origins but rare in MCCs detected so far. MCCs are highly aggressive neuroendocrine tumors with an enhanced potential to metastasize. Until now, less is known about MCC and new approaches to understand this disease are necessary. RNA and DNA were extracted from two MCC cell lines and 27 archival paraffin-embedded patient samples. After reverse transcription, a real-time PCR and a high-resolution melt analysis were carried out. In both MCC cell lines, we could detect a p53 missense mutation at codon 193 (exon 6) with a change in amino acids (His → Leu). This mutation was equal in both cell lines and was investigated in 27 tissue samples in succession to detect possible accounts for the aggressive behavior of MCCs. Unfortunately, no corresponding p53 mutation could be observed in the investigated tissue samples. A new p53 mutation was detected in MCC cell lines. This mutation could not be determined in patients' samples. Therefore, the aggressiveness of MCC seems to be independent of p53 mutations and other mutations might be responsible for developing MCC.
本回顾性分析旨在评估 Merkel 细胞癌 (MCC) 细胞系和 MCC 组织样本中 p53 状态和可能的突变。p53 突变在不同的癌症起源中很常见,但迄今为止在 MCC 中很少发现。MCC 是高度侵袭性的神经内分泌肿瘤,具有较强的转移潜力。到目前为止,对 MCC 的了解较少,需要新的方法来了解这种疾病。从两个 MCC 细胞系和 27 个存档石蜡包埋的患者样本中提取了 RNA 和 DNA。反转录后,进行了实时 PCR 和高分辨率熔解分析。在这两个 MCC 细胞系中,我们都可以在密码子 193 (exon 6) 检测到 p53 错义突变,导致氨基酸发生变化(His → Leu)。该突变在两个细胞系中是相同的,并在 27 个组织样本中进行了连续检测,以寻找可能导致 MCC 侵袭性行为的原因。不幸的是,在研究的组织样本中未观察到相应的 p53 突变。在 MCC 细胞系中检测到一个新的 p53 突变。该突变不能在患者样本中确定。因此,MCC 的侵袭性似乎独立于 p53 突变,其他突变可能负责 MCC 的发生。