Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Blood Rev. 2024 Jul;66:101209. doi: 10.1016/j.blre.2024.101209. Epub 2024 May 7.
Since the discovery of the Philadelphia chromosome in 1960, cytogenetic studies have been instrumental in detecting chromosomal abnormalities that can inform cancer diagnosis, treatment, and risk assessment efforts. The initial expansion of cancer cytogenetics was with fluorescence in situ hybridization (FISH) to assess submicroscopic alterations in dividing or non-dividing cells and has grown into the incorporation of chromosomal microarrays (CMA), and next generation sequencing (NGS). These molecular technologies add additional dimensions to the genomic assessment of cancers by uncovering cytogenetically invisible molecular markers. Rapid technological and bioinformatic advances in NGS are so promising that the idea of performing whole genome sequencing as part of routine patient care may soon become economically and logistically feasible. However, for now cytogenetic studies continue to play a major role in the diagnostic testing and subsequent assessments in leukemia with other genomic studies serving as complementary testing options for detection of actionable genomic abnormalities. In this review, we discuss the role of conventional cytogenetics (karyotyping, chromosome analysis) and FISH studies in hematological malignancies, highlighting the continued clinical utility of these techniques, the subtleties and complexities that are relevant to treating physicians and the unique strengths of cytogenetics that cannot yet be paralleled by the current high-throughput molecular technologies. Additionally, we describe how CMA, optical genome mapping (OGM), and NGS detect abnormalities that were beyond the capacity of cytogenetic studies and how an integrated approach (broad molecular testing) can contribute to the detection of actionable targets and variants in malignancies. Finally, we discuss advances in the field of genomic testing that are bridging the advantages of individual (single) cell based cytogenetic testing and broad genomic testing.
自 1960 年发现费城染色体以来,细胞遗传学研究在检测可用于癌症诊断、治疗和风险评估的染色体异常方面发挥了重要作用。癌症细胞遗传学的最初扩展是使用荧光原位杂交(FISH)来评估分裂或非分裂细胞中的亚微观改变,并发展为染色体微阵列(CMA)和下一代测序(NGS)的纳入。这些分子技术通过揭示细胞遗传学上不可见的分子标记物,为癌症的基因组评估增加了额外的维度。NGS 中的快速技术和生物信息学进步非常有前途,以至于作为常规患者护理一部分进行全基因组测序的想法可能很快在经济和物流上变得可行。然而,目前细胞遗传学研究继续在白血病的诊断测试和后续评估中发挥主要作用,其他基因组研究作为检测可操作基因组异常的互补测试选择。在这篇综述中,我们讨论了常规细胞遗传学(核型分析、染色体分析)和 FISH 研究在血液恶性肿瘤中的作用,强调了这些技术的持续临床应用价值、与治疗医生相关的微妙和复杂性以及细胞遗传学的独特优势,这些优势目前还无法与当前高通量分子技术相媲美。此外,我们描述了 CMA、光学基因组图谱(OGM)和 NGS 如何检测超出细胞遗传学研究能力的异常,以及综合方法(广泛的分子测试)如何有助于检测恶性肿瘤中的可操作靶点和变体。最后,我们讨论了基因组测试领域的进展,这些进展正在弥合基于单个细胞的细胞遗传学测试和广泛的基因组测试的优势。