Genetics of Rare Cancers, IRCCS Ospedale Policlinico San Martino, Largo Rosanna Benzi 10, 16132 Genoa, Italy.
Department of Internal Medicine and Medical Specialties (DiMI), University of Genoa, V.le Benedetto XV 6, 16132 Genoa, Italy.
Genes (Basel). 2024 Jan 16;15(1):104. doi: 10.3390/genes15010104.
The Protection of Telomere 1 () gene was identified as a melanoma predisposition candidate nearly 10 years ago. Thereafter, various cancers have been proposed as associated with germline variants in the context of the so-called Predisposition Tumor Syndrome (POT1-TPD). While the key role, and related risks, of the alterations in in melanoma are established, the correlation between germline variants and the susceptibility to other cancers partially lacks evidence, due also to the rarity of POT1-TPD. Issues range from the absence of functional or segregation studies to biased datasets or the need for a revised classification of variants. Furthermore, a proposal of a surveillance protocol related to the cancers associated with pathogenic variants requires reliable data to avoid an excessive, possibly unjustified, burden for variant carriers. We propose a critical perspective regarding data published over the last 10 years that correlate variants to various types of cancer, other than cutaneous melanoma, to offer food for thought for the specialists who manage cancer predisposition syndromes and to stimulate a debate on the grey areas that have been exposed.
大约 10 年前,人们发现端粒酶 1 () 基因的保护作用与黑色素瘤易感性有关。此后,在所谓的“倾向性肿瘤综合征(POT1-TPD)”背景下,人们提出各种癌症与种系变异有关。虽然已经确定了 改变在黑色素瘤中的关键作用及其相关风险,但由于 POT1-TPD 较为罕见,种系 变异与其他癌症易感性之间的相关性部分缺乏证据,这部分原因是由于缺乏功能或分离研究,也部分归因于数据集存在偏差或需要对变异进行修正分类。此外,制定与种系致病性变异相关的癌症监测方案的建议需要可靠的数据,以避免对变异携带者造成过度的、可能不合理的负担。我们针对过去 10 年发表的与皮肤黑色素瘤以外的各种癌症相关的 变异相关数据提出了批判性观点,为管理癌症易感性综合征的专家提供了思考的素材,并就已经暴露出来的灰色地带问题激发了一场辩论。