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Serglycin promotes breast cancer cell aggressiveness : Induction of epithelial to mesenchymal transition, proteolytic activity and IL-8 signaling

Bouris, Panagiotis (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
Manou, Dimitra (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
Sopaki-Valalaki, Anastasia (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
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Kolokotroni, Anthi (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
Moustakas, Aristidis (författare)
Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Science for Life Laboratory, SciLifeLab
Kapoor, Aastha (författare)
Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA;Thomas Jefferson Univ, Sidney Kimmel Med Coll, Canc Cell Biol & Signaling Program, Philadelphia, PA 19107 USA
Iozzo, Renato V. (författare)
Thomas Jefferson Univ, Sidney Kimmel Med Coll, Dept Pathol Anat & Cell Biol, Philadelphia, PA 19107 USA;Thomas Jefferson Univ, Sidney Kimmel Med Coll, Canc Cell Biol & Signaling Program, Philadelphia, PA 19107 USA
Karamanos, Nikos K. (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
Theocharis, Achilleas D. (författare)
Univ Patras, Dept Chem, Biochem Biochem Anal & Matrix Pathobiol Res Grp, Lab Biochem, GR-26110 Patras, Greece
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 (creator_code:org_t)
ELSEVIER SCIENCE BV, 2018
2018
Engelska.
Ingår i: Matrix Biology. - : ELSEVIER SCIENCE BV. - 0945-053X .- 1569-1802. ; 74, s. 35-51
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Serglycin is an intracellular proteoglycan that is expressed and constitutively secreted by numerous malignant cells, especially prominent in the highly-invasive, triple-negative MDA-MB-231 breast carcinoma cells. Notably, de novo expression of serglycin in low aggressive estrogen receptor alpha (ER alpha)-positive MCF7 breast cancer cells promotes an aggressive phenotype. In this study, we discovered that serglycin promoted epithelial to mesenchymal transition (EMT) in MCF7 cells as shown by increased expression of mesenchymal markers vimentin, fibronectin and EMT-related transcription factor Snail2. These phenotypic traits were also associated with the development of drug resistance toward various chemotherapy agents and induction of their proteolytic potential as shown by the increased expression of matrix metalloproteinases, including MMP-1, MMP-2, MMP-9, MT1-MMP and up-regulation of urokinase-type plasminogen activator. Knockdown of serglycin markedly reduced the expression of these proteolytic enzymes in MDA-MB-231 cells. In addition, serglycin expression was closely linked to a pro-inflammatory gene signature including the chemokine IL-8 in ER alpha-negative breast cancer cells and tumors. Notably, serglycin regulated the secretion of IL-8 in breast cancer cells independently of their ER alpha status and promoted their proliferation, migration and invasion by triggering IL-8/CXCR2 downstream signaling cascades including PI3K, Src and Rac activation. Thus, serglycin promotes the establishment of a pro-inflammatory milieu in breast cancer cells that evokes an invasive mesenchymal phenotype via autocrine activation of IL-8/CXCR2 signaling axis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Proteoglycans
Serglycin
Interleukin-8
Breast cancer
Signaling

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