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Gene dysregulation analysis builds a mechanistic signature for prognosis and therapeutic benefit in colorectal cancer

摘要The implementation of cancer precision medicine requires biomarkers or signatures for predicting prognosis and therapeutic benefits.Most of current efforts in this field are paying much more attention to predictive accuracy than to molecular mechanistic interpretability.Mechanism-driven strategy has recently emerged,aiming to build signatures with both predictive power and explanatory power.Driven by this strategy,we developed a robust gene dysregulation analysis framework with machine learning algorithms,which is capable of exploring gene dysregulations underlying carcinogenesis from high-dimensional data with cooperativity and synergy between regulators and several other transcriptional regulation rules taken into consideration.We then applied the framework to a colorectal cancer (CRC) cohort from The Cancer Genome Atlas.The identified CRC-related dysregulations significantly covered known carcinogenic processes and exhibited good prognostic effect.By choosing dysregulations with greedy strategy,we built a four-dysregulation (4-DysReg) signature,which has the capability of predicting prognosis and adjuvant chemotherapy benefit.4-DysReg has the potential to explain carcinogenesis in terms of dysfunctional transcriptional regulation.These results demonstrate that our gene dysregulation analysis framework could be used to develop predictive signature with mechanistic interpretability for cancer precision medicine,and furthermore,elucidate the mechanisms of carcinogenesis.

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作者 Quanxue Li [1] Wentao Dai [2] Jixiang Liu [3] Qingqing Sang [4] Yi-Xue Li [5] Yuan-Yuan Li [3] 学术成果认领
作者单位 School of Biotechnology, East China University of Science and Technology, Shanghai 200237, China;Shanghai Center for Bioinformation Technology, Shanghai 201203, China [1] Shanghai Center for Bioinformation Technology, Shanghai 201203, China;Department of Surgery, Shanghai Key Laboratory of Gastric Neoplasms, Shanghai Institute of Digestive Surgery, RuiJin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China;Shanghai Engineering Research Center of Pharmaceutical Translation and Shanghai Industrial Technology Institute, Shanghai 201203, China [2] Shanghai Center for Bioinformation Technology, Shanghai 201203, China;Shanghai Engineering Research Center of Pharmaceutical Translation and Shanghai Industrial Technology Institute, Shanghai 201203, China [3] Department of Surgery, Shanghai Key Laboratory of Gastric Neoplasms, Shanghai Institute of Digestive Surgery, RuiJin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, China [4] School of Biotechnology, East China University of Science and Technology, Shanghai 200237, China;Shanghai Center for Bioinformation Technology, Shanghai 201203, China;CAS Key Laboratory of Computational Biology, CAS-MPG Partner Institute for Computational Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China;Shanghai Engineering Research Center of Pharmaceutical Translation and Shanghai Industrial Technology Institute, Shanghai 201203, China [5]
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DOI 10.1093/jmcb/mjaa041
发布时间 2021-04-12(万方平台首次上网日期,不代表论文的发表时间)
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