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Pilocytic astrocytoma: a review of genetic and molecular factors, diagnostic and prognostic markers

机译:多发性星形细胞瘤:遗传和分子因素,诊断和预后标志物的综述

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In spite of numerous studies concerning the pathogenesis of pilocytic astrocytoma (PA), the exact mechanism of the process still remains undetermined. It is difficult to obtain concordance between particular studies, which makes review of existing data especially troublesome. Nevertheless, the most important causative factors seem to be NF1 gene inactivation, in cases related to neurofibromatosis type 1, and BRAF gene overexpression in sporadic PAs, both resulting in MAPK/Erk pathway upregulation. Other molecular alterations, like mTOR or PI3K pathway deregulation, or Matrilin 2 overexpression, may influence the course of the disease, leading to the development of more aggressive and recurrent tumors. In the current paper we review genetic alterations in PA and describe currently studied molecular markers that may contribute to the development of the tumor and can be used in pathological staging of the malformation.
机译:尽管进行了许多有关毛细胞星形细胞瘤(PA)发病机理的研究,但该过程的确切机制仍未确定。特定研究之间很难取得一致,这使得对现有数据的审查特别麻烦。尽管如此,最重要的致病因素似乎是NF1基因失活(与1型神经纤维瘤病有关)和散发性PA中的BRAF基因过度表达,两者均导致MAPK / Erk通路上调。其他分子改变,例如mTOR或PI3K通路失调或Matrilin 2过表达,可能会影响疾病进程,导致更具侵略性和复发性肿瘤的发展。在当前的论文中,我们回顾了PA的遗传改变,并描述了目前研究的分子标记物,这些分子标记物可能有助于肿瘤的发展,并可以用于畸形的病理分期。

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