Department of Medical Sciences, University of Turin, Turin, Italy; Candiolo Cancer Institute, FPO-IRCCS, Candiolo, TO, Italy.
Candiolo Cancer Institute, FPO-IRCCS, Candiolo, TO, Italy.
Lab Invest. 2024 Jan;104(1):100280. doi: 10.1016/j.labinv.2023.100280. Epub 2023 Oct 30.
Formalin-fixed paraffin-embedded (FFPE) samples represent the cornerstone of tissue-based analysis in precision medicine. Targeted next-generation sequencing panels are routinely used to analyze a limited number of genes to guide treatment decision-making for advanced-stage patients. The number and complexity of genetic alterations to be investigated are rapidly growing; in several instances, a comprehensive genomic profiling analysis is needed. The poor quality of genetic material extracted from FFPE samples may impact the feasibility/reliability of sequencing data. We sampled 9 colorectal cancers to allow 4 parallel fixations: (1) neutral buffered formalin (NBF), (2) acid-deprived formalin fixation (ADF), (3) precooled ADF (coldADF), and (4) glyoxal acid free (GAF). DNA extraction, fragmentation analysis, and sequencing by 2 large next-generation sequencing panels (OCAv3 and TSO500) followed. We comprehensively analyzed library and sequencing quality controls and the quality of sequencing results. Libraries from coldADF samples showed significantly longer reads than the others with both panels. ADF-derived and coldADF-derived libraries showed the lowest level of noise and the highest levels of uniformity with the OCAv3 panel, followed by GAF and NBF samples. The data uniformity was confirmed by the TSO500 results, which also highlighted the best performance in terms of the total region sequenced for the ADF and coldADF samples. NBF samples had a significantly smaller region sequenced and displayed a significantly lower number of evaluable microsatellite loci and a significant increase in single-nucleotide variations compared with other protocols. Mutational signature 1 (aging and FFPE artifact related) showed the highest (37%) and lowest (17%) values in the NBF and coldADF samples, respectively. Most of the identified genetic alterations were shared by all samples in each lesion. Five genes showed a different mutational status across samples and/or panels: 4 discordant results involved NBF samples. In conclusion, acid-deprived fixatives (GAF and ADF) guarantee the highest DNA preservation/sequencing performance, thus allowing more complex molecular profiling of tissue samples.
福尔马林固定石蜡包埋(FFPE)样本是精准医学中组织分析的基石。靶向下一代测序面板通常用于分析有限数量的基因,以指导晚期患者的治疗决策。待研究的遗传改变的数量和复杂性正在迅速增加;在某些情况下,需要进行全面的基因组分析。从 FFPE 样本中提取的遗传物质的质量较差可能会影响测序数据的可行性/可靠性。我们采集了 9 例结直肠癌样本,允许进行 4 种平行固定:(1)中性缓冲福尔马林(NBF),(2)酸剥夺福尔马林固定(ADF),(3)预冷 ADF(冷 ADF),和(4)无乙二醛酸(GAF)。随后进行 DNA 提取、片段分析和两种大型下一代测序面板(OCAv3 和 TSO500)测序。我们全面分析了文库和测序质量控制以及测序结果的质量。与其他两种面板相比,冷 ADF 样本的文库显示出明显更长的读长。ADF 衍生和冷 ADF 衍生的文库与 OCAv3 面板显示出最低的噪声水平和最高的均匀性,其次是 GAF 和 NBF 样本。TSO500 的结果证实了数据的均匀性,同时也突出了 ADF 和冷 ADF 样本中测序的总区域的最佳性能。NBF 样本测序的区域明显较小,与其他方案相比,可评估的微卫星位点数量明显减少,单核苷酸变异数量明显增加。突变特征 1(与衰老和 FFPE 人工制品相关)在 NBF 和冷 ADF 样本中分别显示出最高(37%)和最低(17%)的值。大多数鉴定的遗传改变在每个病变的所有样本中都有共享。有 5 个基因在不同样本和/或面板中显示出不同的突变状态:4 个不一致的结果涉及 NBF 样本。总之,酸剥夺固定剂(GAF 和 ADF)保证了最高的 DNA 保存/测序性能,从而允许对组织样本进行更复杂的分子分析。