| Literature DB >> 28866366 |
Carlos Alfaro1, Miguel F Sanmamed2, María E Rodríguez-Ruiz3, Álvaro Teijeira4, Carmen Oñate5, Álvaro González6, Mariano Ponz3, Kurt A Schalper7, José L Pérez-Gracia8, Ignacio Melero9.
Abstract
Interleukin-8 (CXCL8) was originally described asa chemokine whose main function is the attraction of a polymorphonuclear inflammatory leukocyte infiltrate acting on CXCR1/2. Recently, it has been found that tumors very frequently coopt the production of this chemokine, which in this malignant context exerts different pro-tumoral functions. Reportedly, these include angiogenesis, survival signaling for cancer stem cells and attraction of myeloid cells endowed with the ability to immunosuppress and locally provide growth factors. Given the fact that in cancer patients IL-8 is mainly produced by tumor cells themselves, its serum concentration has been shown to correlate with tumor burden. Thus, IL-8 serum concentrations have been shown to be useful asa pharmacodynamic biomarker to early detect response to immunotherapy. Finally, because of the roles that IL-8 plays in favoring tumor progression, several therapeutic strategies are being developed to interfere with its functions. Such interventions hold promise, especially for therapeutic combinations in the field of cancer immunotherapy.Entities:
Keywords: CXCR1/2; Cancer therapeutic agents; IL-8 (CXCL8); Immunotherapy; Myeloid-derived suppressor cells; Pharmacodynamic biomarker
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Year: 2017 PMID: 28866366 DOI: 10.1016/j.ctrv.2017.08.004
Source DB: PubMed Journal: Cancer Treat Rev ISSN: 0305-7372 Impact factor: 12.111