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SDHB 和 SDHD 相关副神经节瘤疾病动力学的数学建模:进一步了解遗传性肿瘤差异和未来治疗策略。

Mathematical modeling of disease dynamics in SDHB- and SDHD-related paraganglioma: Further step in understanding hereditary tumor differences and future therapeutic strategies.

机构信息

Aix-Marseille University, School of Pharmacy of Marseille, Simulation & Modelling: Adaptive Response for Therapeutics in Cancer (SMARTc), Marseille, France.

INSERM UMR U1068, CNRS UMR 7258, Aix-Marseille University, Cancer Research Center of Marseille, Marseille, France.

出版信息

PLoS One. 2018 Aug 14;13(8):e0201303. doi: 10.1371/journal.pone.0201303. eCollection 2018.

Abstract

Succinate dehydrogenase subunit B and D (SDHB and SDHD) mutations represent the most frequent cause of hereditary pheochromocytoma and paraganglioma (PPGL). Although truncation of the succinate dehydrogenase complex is thought to be the disease causing mechanism in both disorders, SDHB and SDHD patients exihibit different phenotypes. These phenotypic differences are currently unexplained by molecular genetics. The aim of this study is to compare disease dynamics in these two conditions via a Markov chain model based on 4 clinically-defined steady states. Our model corroborates at the population level phenotypic observations in SDHB and SDHD carriers and suggests potential explanations associated with the probabilities of disease maintenance and regression. In SDHB-related syndrome, PPGL maintenance seems to be reduced compared to SDHD (p = 0.04 vs 0.95) due to higher probability of tumor cell regression in SDHB vs SDHD (p = 0.87 vs 0.00). However, when SDHB-tumors give rise to metastases, metastatic cells are able to thrive with decreased probability of regression compared with SDHD counterparts (p = 0.17 vs 0.89). By constrast, almost all SDHD patients develop PGL (mainly head and neck) that persist throughout their lifetime. However, compared to SDHB, maintenance of metastatic lesions seems to be less effective for SDHD (p = 0.83 vs 0.11). These findings align with data suggesting that SDHD-related PPGL require less genetic events for tumor initiation and maintenance compared to those related to SDHB, but fail to initiate biology that promotes metastatic spread and metastatic cell survival in host tissues. By contrast, the higher number of genetic abnormalities required for tumor initiation and maintenance in SDHB PPGL result in a lower penetrance of PGL, but when cells give rise to metastases they are assumed to be better adapted to sustain survival. These proposed differences in disease progression dynamics between SDHB and SDHD diseases provide new cues for future exploration of SDHx PPGL behavior, offering considerations for future specific therapeutic and prevention strategies.

摘要

琥珀酸脱氢酶亚基 B 和 D(SDHB 和 SDHD)突变是遗传性嗜铬细胞瘤和副神经节瘤(PPGL)最常见的原因。尽管琥珀酸脱氢酶复合物的截断被认为是这两种疾病的致病机制,但 SDHB 和 SDHD 患者表现出不同的表型。目前,这些表型差异无法用分子遗传学来解释。本研究旨在通过基于 4 种临床定义的稳定状态的马尔可夫链模型来比较这两种疾病的疾病动态。我们的模型在人群水平上证实了 SDHB 和 SDHD 携带者的表型观察结果,并提出了与疾病维持和消退概率相关的潜在解释。在 SDHB 相关综合征中,与 SDHD 相比(p=0.04 对 0.95),PPGL 的维持似乎减少,这是由于 SDHB 中肿瘤细胞消退的概率高于 SDHD(p=0.87 对 0.00)。然而,当 SDHB 肿瘤发生转移时,与 SDHD 相比,转移细胞能够在降低的消退概率下存活(p=0.17 对 0.89)。相比之下,几乎所有的 SDHD 患者都会患上 PGL(主要是头颈部),并在其一生中持续存在。然而,与 SDHB 相比,SDHD 维持转移性病变的效果似乎较差(p=0.83 对 0.11)。这些发现与数据一致,表明与 SDHB 相关的 PPGL 相比,SDHD 相关的 PPGL 启动和维持肿瘤所需的遗传事件较少,但未能启动促进转移扩散和转移细胞在宿主组织中存活的生物学。相比之下,SDHB PPGL 中肿瘤启动和维持所需的遗传异常数量较多导致 PGL 的外显率较低,但当细胞发生转移时,它们被认为更能适应维持生存。SDHB 和 SDHD 疾病之间疾病进展动态的这些差异为未来探索 SDHx PPGL 的行为提供了新的线索,并为未来特定的治疗和预防策略提供了考虑因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/803d/6091916/8216e2efd5fa/pone.0201303.g001.jpg

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