Leptin utilizes Jun N-terminal kinases to stimulate the invasion of MCF-7 breast cancer cells

Vanity McMurtry, Ann Marie Simeone, René Nieves-Alicea, Ana M. Tari

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

Abstract

In breast tumors, high levels of leptin have been associated with increased incidence of breast cancer metastasis. Breast cancer metastasis is directly associated with breast cancer cell invasion. However, whether leptin could augment breast cancer cell invasion is not known. Here we showed that leptin increased the invasiveness and the matrix metallo-proteinase-2 (MMP-2) activity of the MCF-7 breast cancer cell line. Leptin stimulated the phosphorylation of extracellular signals regulated kinases, signal transducers and activators of transcription 3 and Jun N-terminal kinases (JNK); however, only inhibition of JNK decreased leptin-mediated activation of MMP-2. Furthermore, inhibition of JNK suppressed leptin-mediated breast cancer cell invasion. Here we report the novel findings that leptin increased invasion of breast cancer cells by activating JNK, resulting in increased MMP-2 activity.

Original languageEnglish (US)
Pages (from-to)197-204
Number of pages8
JournalClinical and Experimental Metastasis
Volume26
Issue number3
DOIs
StatePublished - Mar 2009

Keywords

  • Breast cancer invasion
  • Extracellular signals regulated kinases
  • Jun N-terminal kinases
  • Leptin
  • Matrix metallo-proteinase-2
  • Signal transducers and activators of transcription 3

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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