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转录组负担分析确定血液系统恶性肿瘤和实体瘤的生物学进展路线图。

An Analysis of Transcriptomic Burden Identifies Biological Progression Roadmaps for Hematological Malignancies and Solid Tumors.

作者信息

Ravi Dashnamoorthy, Beheshti Afshin, Burgess Kristine, Kritharis Athena, Chen Ying, Evens Andrew M, Parekkadan Biju

机构信息

Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, NJ 08901, USA.

KBR, Space Biosciences Division, National Aeronautical and Space Administration, Ames Research Center, Moffett Field, CA 94035, USA.

出版信息

Biomedicines. 2022 Oct 27;10(11):2720. doi: 10.3390/biomedicines10112720.

Abstract

Biological paths of tumor progression are difficult to predict without time-series data. Using median shift and abacus transformation in the analysis of RNA sequencing data sets, natural patient stratifications were found based on their transcriptomic burden (TcB). Using gene-behavior analysis, TcB groups were evaluated further to discover biological courses of tumor progression. We found that solid tumors and hematological malignancies (n = 4179) share conserved biological patterns, and biological network complexity decreases at increasing TcB levels. An analysis of gene expression datasets including pediatric leukemia patients revealed TcB patterns with biological directionality and survival implications. A prospective interventional study with PI3K targeted therapy in canine lymphomas proved that directional biological responses are dynamic. To conclude, TcB-enriched biological mechanisms detected the existence of biological trajectories within tumors. Using this prognostic informative novel informatics method, which can be applied to tumor transcriptomes and progressive diseases inspires the design of progression-specific therapeutic approaches.

摘要

没有时间序列数据,肿瘤进展的生物学路径很难预测。在RNA测序数据集分析中使用中位数移动和算盘转换,根据患者的转录组负担(TcB)发现了自然的患者分层。通过基因行为分析,对TcB组进行进一步评估以发现肿瘤进展的生物学过程。我们发现实体瘤和血液系统恶性肿瘤(n = 4179)具有保守的生物学模式,并且随着TcB水平的升高,生物网络复杂性降低。对包括小儿白血病患者在内的基因表达数据集的分析揭示了具有生物学方向性和生存意义的TcB模式。一项针对犬淋巴瘤的PI3K靶向治疗的前瞻性干预研究证明,定向生物学反应是动态的。总之,富含TcB的生物学机制检测到肿瘤内生物学轨迹的存在。使用这种可应用于肿瘤转录组和进行性疾病的具有预后信息的新型信息学方法,激发了针对进展特异性治疗方法的设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5e9/9687799/a88ddd1eb898/biomedicines-10-02720-g001.jpg

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