4.8 Article

Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells

期刊

MOLECULAR CELL
卷 76, 期 5, 页码 838-+

出版社

CELL PRESS
DOI: 10.1016/j.molcel.2019.08.028

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资金

  1. American Association for Cancer Research [15 40 01 CAIL]
  2. Howard Hughes Medical Institute
  3. National Cancer Institute (NCI) [R35CA22044901]
  4. Cancer Prevention and Research Institute of Texas (CPRIT) [RP160089]
  5. Robert A. Welch Foundation [I-1733]
  6. Robert L. Moody, Sr. Faculty Scholar Endowment
  7. Joel B. Steinberg, M.D. Chair in Pediatrics
  8. CPRIT [RP160652]
  9. NCI [P50CA70907]

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Intermediary metabolism in cancer cells is regulated by diverse cell-autonomous processes, including signal transduction and gene expression patterns, arising from specific oncogenotypes and cell lineages. Although it is well established that metabolic reprogramming is a hallmark of cancer, we lack a full view of the diversity of metabolic programs in cancer cells and an unbiased assessment of the associations between metabolic pathway preferences and other cell-autonomous processes. Here, we quantified metabolic features, mostly from the C-13 enrichment of molecules from central carbon metabolism, in over 80 non-small cell lung cancer (NSCLC) cell lines cultured under identical conditions. Because these cell lines were extensively annotated for oncogenotype, gene expression, protein expression, and therapeutic sensitivity, the resulting database enables the user to uncover new relationships between metabolism and these orthogonal processes.

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