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CXADR-Mediated Formation of an AKT Inhibitory Signalosome at Tight Junctions Controls Epithelial-Mesenchymal Plasticity in Breast Cancer.

Nilchian, Azadeh (author)
Karolinska Institutet
Johansson, Joel (author)
Karolinska Institutet
Ghalali, Aram (author)
Karolinska Inst, Inst Environm Med, Stockholm, Sweden;Harvard Med Sch, Boston Childrens Hosp, Boston, MA USA
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Travica Asanin, Sandra (author)
Karolinska Inst, Dept Microbiol Tumor & Cell Biol MTC, Stockholm, Sweden
Santiago, Ana (author)
Karolinska Inst, Dept Microbiol Tumor & Cell Biol MTC, Stockholm, Sweden
Rosencrantz, Oskar (author)
Karolinska Inst, Dept Microbiol Tumor & Cell Biol MTC, Stockholm, Sweden
Vincent, C. Theresa (author)
Uppsala universitet,Institutionen för immunologi, genetik och patologi,Karolinska Inst, Dept Physiol & Pharmacol, Stockholm, Sweden;Weill Cornell Med, Dept Physiol & Biophys, New York, NY USA
Sollerbrant, Kerstin (author)
Karolinska Inst, Dept Womens & Childrens Hlth, Stockholm, Sweden;Univ Hosp, Stockholm, Sweden
Sund, Malin (author)
Umeå universitet,Kirurgi,Umea Univ, Dept Surg & Perioperat Sci, Umea, Sweden
Stenius, Ulla (author)
Karolinska Institutet
Fuxe, Jonas (author)
Karolinska Inst, Dept Microbiol Tumor & Cell Biol MTC, Stockholm, Sweden
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 (creator_code:org_t)
American Association for Cancer Research, 2019
2019
English.
In: Cancer Research. - : American Association for Cancer Research. - 0008-5472 .- 1538-7445. ; 79:1, s. 47-60
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Tight junctions (TJ) act as hubs for intracellular signaling pathways controlling epithelial cell fate and function. Deregulation of TJ is a hallmark of epithelial-mesenchymal transition (EMT), which contributes to carcinoma progression and metastasis. However, the signaling mechanisms linking TJ to the induction of EMT are not understood. Here we identify a TJ-based signalosome, which controls AKT signaling and EMT in breast cancer. The coxsackie- and adenovirus receptor (CXADR), a TJ protein with an essential yet uncharacterized role in organogenesis and tissue homeostasis, was identified as a key component of the signalosome. CXADR regulated the stability and function of the phosphatases and AKT inhibitors PTEN and PHLPP2. Loss of CXADR led to hyper-activation of AKT and sensitized cells to TGF-β1-induced EMT. Conversely, restoration of CXADR stabilized PHLPP2 and PTEN, inhibited AKT, and promoted epithelial differentiation. Loss of CXADR in luminal A breast cancer correlated with loss of PHLPP2 and PTEN and poor prognosis. These results show that CXADR promotes the formation of an AKT-inhibitory signalosome at TJ and regulates epithelial-mesenchymal plasticity in breast cancer cells. Moreover, loss of CXADR might be used as a prognostic marker in luminal breast cancer.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

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