Biological Response Modifier in Cancer Immunotherapy

Adv Exp Med Biol. 2016:909:69-138. doi: 10.1007/978-94-017-7555-7_2.

Abstract

Biological response modifiers (BRMs) emerge as a lay of new compounds or approaches used in improving cancer immunotherapy. Evidences highlight that cytokines, Toll-like receptor (TLR) signaling, and noncoding RNAs are of crucial roles in modulating antitumor immune response and cancer-related chronic inflammation, and BRMs based on them have been explored. In particular, besides some cytokines like IFN-α and IL-2, several Toll-like receptor (TLR) agonists like BCG, MPL, and imiquimod are also licensed to be used in patients with several malignancies nowadays, and the first artificial small noncoding RNA (microRNA) mimic, MXR34, has entered phase I clinical study against liver cancer, implying their potential application in cancer therapy. According to amounts of original data, this chapter will review the regulatory roles of TLR signaling, some noncoding RNAs, and several key cytokines in cancer and cancer-related immune response, as well as the clinical cases in cancer therapy based on them.

Keywords: Biological response modifiers; Cancer immunotherapy; Cytokines; Noncoding RNAs; Toll-like receptor.

Publication types

  • Review

MeSH terms

  • Aminoquinolines / therapeutic use*
  • Antineoplastic Agents / therapeutic use*
  • Clinical Trials as Topic
  • Gene Expression Regulation, Neoplastic / immunology*
  • Humans
  • Imiquimod
  • Immunologic Factors / therapeutic use*
  • Immunotherapy / methods*
  • Interferon-alpha / genetics
  • Interferon-alpha / immunology
  • Interleukin-2 / genetics
  • Interleukin-2 / immunology
  • Mycobacterium bovis / genetics
  • Mycobacterium bovis / immunology
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / pathology
  • Neoplasms / therapy*
  • RNA, Untranslated / genetics
  • RNA, Untranslated / immunology
  • RNA, Untranslated / therapeutic use
  • Receptors, Thrombopoietin / genetics
  • Receptors, Thrombopoietin / immunology
  • Signal Transduction
  • Toll-Like Receptors / agonists
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / immunology

Substances

  • Aminoquinolines
  • Antineoplastic Agents
  • Immunologic Factors
  • Interferon-alpha
  • Interleukin-2
  • RNA, Untranslated
  • Receptors, Thrombopoietin
  • Toll-Like Receptors
  • MPL protein, human
  • Imiquimod