Baltzarsen Pii B, Georgsen Jeanette B, Nielsen Patricia S, Steiniche Torben, Stougaard Magnus
Department of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Appl Immunohistochem Mol Morphol. 2020 Jan;28(1):36-41. doi: 10.1097/PAI.0000000000000690.
Telomerase is reactivated in most cancers and is possibly an early driver event in melanoma. Our aim was to test a novel in situ hybridization technique, RNAscope, for the detection of human telomerase reverse transcriptase (hTERT) mRNA in archival formalin-fixed, paraffin-embedded (FFPE) tissue and to compare the mRNA expression of melanomas and benign naevi. Furthermore, we wanted to see if hTERT mRNA could be a diagnostic or prognostic marker of melanoma. In situ hybridization for the detection of hTERT mRNA was performed on FFPE tissue of 17 melanomas and 13 benign naevi. We found a significant difference in the expression of hTERT mRNA between melanomas and benign naevi (P<0.001) and the expression of hTERT mRNA correlated with Breslow thickness (ρ=0.56, P=0.0205) and the Ki67 proliferation index (ρ=0.72, P=0.001). This study showed that RNAscope was a reliable in situ hybridization method for the detection of hTERT mRNA in FFPE tissue of melanomas and benign naevi. hTERT mRNA was more abundantly expressed in melanomas compared with benign naevi, but cannot be used solely as a diagnostic marker due to an overlap in expression. The hTERT mRNA expression in melanomas correlated with the prognostic markers Breslow thickness and the Ki67 index indicating a prognostic potential of hTERT mRNA.
端粒酶在大多数癌症中被重新激活,可能是黑色素瘤早期的驱动事件。我们的目的是测试一种新型原位杂交技术——RNAscope,用于检测存档的福尔马林固定、石蜡包埋(FFPE)组织中的人端粒酶逆转录酶(hTERT)mRNA,并比较黑色素瘤和良性痣的mRNA表达。此外,我们想看看hTERT mRNA是否可以作为黑色素瘤的诊断或预后标志物。对17例黑色素瘤和13例良性痣的FFPE组织进行了检测hTERT mRNA的原位杂交。我们发现黑色素瘤和良性痣之间hTERT mRNA的表达存在显著差异(P<0.001),并且hTERT mRNA的表达与Breslow厚度(ρ=0.56,P=0.0205)和Ki67增殖指数(ρ=0.72,P=0.001)相关。这项研究表明,RNAscope是一种可靠的原位杂交方法,用于检测黑色素瘤和良性痣的FFPE组织中的hTERT mRNA。与良性痣相比,hTERT mRNA在黑色素瘤中表达更丰富,但由于表达存在重叠,不能单独用作诊断标志物。黑色素瘤中hTERT mRNA的表达与预后标志物Breslow厚度和Ki67指数相关,表明hTERT mRNA具有预后潜力。