4.8 Article

Growth of Triple-Negative Breast Cancer Cells Relies upon Coordinate Autocrine Expression of the Proinflammatory Cytokines IL-6 and IL-8

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CANCER RESEARCH
卷 73, 期 11, 页码 3470-3480

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AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-12-4524-T

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  1. AstraZeneca
  2. Celgene
  3. CeMines
  4. Exelixis/Sanofi
  5. GSK
  6. Roche
  7. Wyeth/Pfizer/Puma
  8. Cancer Center Support Grant (CCSG) [1CA16672]
  9. Susan G. Komen Promise grant [KG081694]
  10. Komen SAB grant [9SAB12-00006]

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Triple-negative breast cancers (TNBC) are aggressive with no effective targeted therapies. A combined database analysis identified 32 inflammation-related genes differentially expressed in TNBCs and 10 proved critical for anchorage-independent growth. In TNBC cells, an LPA-LPAR2-EZH2 NF-kappa B signaling cascade was essential for expression of interleukin (IL)-6, IL-8, and CXCL1. Concurrent inhibition of IL-6 and IL-8 expression dramatically inhibited colony formation and cell survival in vitro and stanched tumor engraftment and growth in vivo. A Cox multivariable analysis of patient specimens revealed that IL-6 and IL-8 expression predicted patient survival times. Together these findings offer a rationale for dual inhibition of IL-6/IL-8 signaling as a therapeutic strategy to improve outcomes for patients with TNBCs. (C) 2013 AACR.

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