Hormann Femke M, Hoogkamer Alex Q, Boeree Aurélie, Sonneveld Edwin, Escherich Gabriele, den Boer Monique L, Boer Judith M
Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Oncode Institute, Utrecht, Netherlands.
Front Oncol. 2023 Feb 23;13:1128560. doi: 10.3389/fonc.2023.1128560. eCollection 2023.
Intrachromosomal amplification of chromosome 21 (iAMP21) is a rare subtype of B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). It is unknown how iAMP21 contributes to leukaemia. The currently known commonly amplified region is 5.1 Mb.
We aimed to narrow down the common region of amplification by using high resolution techniques. Array comparative genomic hybridization (aCGH) was used to determine copy number aberrations, Affymetrix U133 Plus2 expression arrays were used to determine gene expression. Genome-wide expression correlations were evaluated using Globaltest.
We narrowed down the common region of amplification by combining copy number data from 12 iAMP21 cases with 52 cases from literature. The combined common region of amplification was 1.57 Mb, located from 36.07 to 37.64 Mb (GRCh38). This region is located telomeric from, but not including, , which is the locus commonly used to diagnose iAMP21. This narrow region, which falls inside the Down Syndrome critical region, includes 13 genes of which the expression of eight genes was significantly upregulated compared with 143 non-iAMP21 B-other cases. Among these, transcriptional repressor (also known as ) was the highest overexpressed gene (fold change = 4.2, FDR < 0.001) and most strongly correlated (R = 0.58) with iAMP21-related genome-wide expression changes.
The more precise definition of the common region of amplification could be beneficial in the diagnosis of iAMP21 based on copy number analysis from DNA sequencing or arrays as well as stimulate functional research into the role of the included genes in iAMP21 biology.
21号染色体的染色体内扩增(iAMP21)是B细胞前体急性淋巴细胞白血病(BCP-ALL)的一种罕见亚型。目前尚不清楚iAMP21如何导致白血病。目前已知的常见扩增区域为5.1 Mb。
我们旨在通过使用高分辨率技术缩小扩增的常见区域。采用阵列比较基因组杂交(aCGH)来确定拷贝数变异,使用Affymetrix U133 Plus2表达阵列来确定基因表达。使用Globaltest评估全基因组表达相关性。
我们将来自12例iAMP21病例的拷贝数数据与文献中的52例病例相结合,从而缩小了扩增的常见区域。合并后的常见扩增区域为1.57 Mb,位于36.07至37.64 Mb(GRCh38)。该区域位于端粒位置,但不包括,后者是常用于诊断iAMP21的位点。这个狭窄区域位于唐氏综合征关键区域内,包含13个基因,其中8个基因的表达与143例非iAMP21 B-其他病例相比显著上调。其中,转录抑制因子(也称为)是过表达最高的基因(倍数变化 = 4.2,FDR < 0.001),并且与iAMP21相关的全基因组表达变化相关性最强(R = 0.58)。
扩增常见区域的更精确定义可能有助于基于DNA测序或阵列的拷贝数分析诊断iAMP21,并促进对所包含基因在iAMP21生物学中作用的功能研究。