Department of Immunology, Faculty of Medicine and Dentistry, Palacký University and University Hospital Olomouc, Olomouc, Czech Republic.
Department of Computer Science, Faculty of Electrical Engineering and Computer Science, VSB-Technical University of Ostrava, Ostrava, Czech Republic.
Br J Haematol. 2022 Nov;199(3):371-381. doi: 10.1111/bjh.18419. Epub 2022 Aug 26.
Germline pathogenic ATM (ataxia-telangiectasia mutated) variants are associated with the risk of multiple cancers; however, genetic testing reveals a large number of ATM variants of uncertain significance (VUS). Here, we studied germline ATM variants occurring in a real-world cohort of 336 patients with chronic lymphocytic leukaemia (CLL) and public cancer whole-exome/genome-sequencing datasets (445 CLL, 75 mantle cell lymphoma, 216 metastatic breast cancer, 140 lung cancer patients). We found that two-thirds of rare germline ATM variants are pathogenic (18%-50%) or VUS-predicted pathogenic (50%-82%), depending on cancer type and reaching a prevalence of up to 8%, and one-third are VUS-predicted benign. Patients with both pathogenic and VUS-predicted pathogenic variants, all heterozygous, mostly missense, are more predisposed to biallelic ATM inactivation by acquiring deletion (del)11q than patients without these variants, similar to patients with somatic ATM variants. A functional assay of ATM activity in primary CLL cells proved that VUS-predicted pathogenic ATM variants partially reduce ATM activity and concurrent del(11q) leads to complete loss of ATM activity. The rare germline variants were associated with reduced progression-free survival in CLL on novel agents, comparable to somatic ATM or TP53 disruptions. Our results highlight the need to determine the pathogenicity of VUS in clinically relevant genes such as ATM.
胚系致病性 ATM(共济失调毛细血管扩张突变)变异与多种癌症的风险相关;然而,基因检测揭示了大量意义不确定的 ATM 变异体(VUS)。在这里,我们研究了发生在 336 例慢性淋巴细胞白血病(CLL)患者的真实队列和公共癌症全外显子/基因组测序数据集中的胚系 ATM 变异体(445 例 CLL、75 例套细胞淋巴瘤、216 例转移性乳腺癌、140 例肺癌患者)。我们发现,三分之二的罕见胚系 ATM 变异体是致病性的(18%-50%)或预测致病性的 VUS(50%-82%),这取决于癌症类型,患病率高达 8%,三分之一是预测良性的 VUS。所有为杂合子的致病性和预测致病性的 VUS 变异体的患者,大多为错义突变,比没有这些变异体的患者更容易通过获得 11q 缺失(del)而导致双等位基因 ATM 失活,与具有体细胞 ATM 变异体的患者相似。对原发性 CLL 细胞中 ATM 活性的功能测定证明,预测致病性的 VUS-ATM 变异体部分降低了 ATM 活性,而同时发生的 del(11q)则导致 ATM 活性完全丧失。罕见的胚系变异与新型药物治疗 CLL 时无进展生存期的缩短有关,与体细胞 ATM 或 TP53 缺失相当。我们的研究结果强调了需要确定临床相关基因(如 ATM)中 VUS 的致病性。