Rabab'h Omar, Gharaibeh Abeer, Al-Ramadan Ali, Ismail Manar, Shah Jawad
Insight Research Institute, Flint, MI 48507, USA.
Center for Cognition and Neuroethics, University of Michigan-Flint, Flint, MI 48502, USA.
Cancers (Basel). 2021 Aug 1;13(15):3880. doi: 10.3390/cancers13153880.
Neurofibromatosis type 1 is an autosomal dominant genetic disease and a common tumor predisposition syndrome that affects 1 in 3000 to 4000 patients in the USA. Although studies have been conducted to better understand and manage this disease, the underlying pathogenesis of neurofibromatosis type 1 has not been completely elucidated, and this disease is still associated with significant morbidity and mortality. Treatment options are limited to surgery with chemotherapy for tumors in cases of malignant transformation. In this review, we summarize the advances in the development of targeted pharmacological interventions for neurofibromatosis type 1 and related conditions.
1型神经纤维瘤病是一种常染色体显性遗传病,也是一种常见的肿瘤易患综合征,在美国每3000至4000名患者中就有1人受其影响。尽管已经开展了多项研究以更好地了解和管理这种疾病,但1型神经纤维瘤病的潜在发病机制尚未完全阐明,并且这种疾病仍与显著的发病率和死亡率相关。对于发生恶变的肿瘤,治疗选择仅限于手术加化疗。在这篇综述中,我们总结了1型神经纤维瘤病及相关病症靶向药物干预开发方面的进展。