4.8 Article

Machine Learning Identifies Stemness Features Associated with Oncogenic Dedifferentiation

期刊

CELL
卷 173, 期 2, 页码 338-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2018.03.034

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资金

  1. NIH [U54 HG003273, U54 HG003067, U54 HG003079, U24 CA143799, U24 CA143835, U24 CA143840, U24 CA143843, U24 CA143845, U24 CA143848, U24 CA143858, U24 CA143866, U24 CA143867, U24 CA143882, U24 CA143883, U24 CA144025, P30 CA016672]
  2. NCI [5R01CA180778, 3U24CA143858, 1U24CA210990, 5U54HG006097, 1U24CA210949, 1U24CA210950]
  3. NIGMS [5R01GM109031]
  4. Henry Ford Cancer Institute's Early Career Investigator Award [A20054]
  5. Sao Paulo Research Foundation (FAPESP) [2014/02245-3, 2016/01975-3]
  6. FAPESP [2014/08321-3, 2015/07925-5, 2016/01389-7, 2016/10436-9, 2016/06488-3, 2016/12329-5, 2016/15485-8]
  7. Henry Ford Hospital [A30935]
  8. Spanish Institute of Health Carlos III [CP14/00229]
  9. CPRIT [RP13039]
  10. Michael & Susan Dell Foundation grant The Lorraine Dell Program in Bioinformatics''
  11. Polish Science Foundation Welcome grant [2010/3-3]
  12. Mary K. Chapman Foundation gift Chapman Foundation Fund for Bioinformatics''
  13. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [16/01975-3, 14/08321-3, 16/15485-8, 16/06488-3] Funding Source: FAPESP

向作者/读者索取更多资源

Cancer progression involves the gradual loss of a differentiated phenotype and acquisition of progenitor and stem-cell-like features. Here, we provide novel stemness indices for assessing the degree of oncogenic dedifferentiation. We used an innovative one-class logistic regression (OCLR) machine-learning algorithm to extract transcriptomic and epigenetic feature sets derived from non-transformed pluripotent stem cells and their differentiated progeny. Using OCLR, we were able to identify previously undiscovered biological mechanisms associated with the dedifferentiated oncogenic state. Analyses of the tumor microenvironment revealed unanticipated correlation of cancer stemness with immune checkpoint expression and infiltrating immune cells. We found that the dedifferentiated oncogenic phenotype was generally most prominent in metastatic tumors. Application of our stemness indices to single-cell data revealed patterns of intra-tumor molecular heterogeneity. Finally, the indices allowed for the identification of novel targets and possible targeted therapies aimed at tumor differentiation.

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