방사선생물학

본문글자크기
  • 2017년 02월호
    [Biochem Biophys Res Commun.] APBB1 reinforces cancer stem cell and epithelial-to-mesenchymal transition by regulating the IGF1R signaling pathway in non-small-cell lung cancer cells.

    KAERI/ 이제하, 김인규*

  • 출처
    Biochem Biophys Res Commun.
  • 등재일
    2017 Jan 1
  • 저널이슈번호
    482(1):35-42. doi: 10.1016/j.bbrc.2016.11.030. Epub 2016 Nov 9.
  • 내용

    바로가기  >

     Abstract

    Amyloid β precursor protein binding family B member 1(APBB1) was first identified as a binding partner of amyloid precursor protein during brain development, but its function in the context of cancer remain unclear. Here we show for the first time that APBB1 is partly associated with intensifying cancer stem cell(CSC) and epithelial-to-mesenchymal transition (EMT) and enhancing radiation-resistant properties of lung cancer cells. We found that APBB1 was highly expressed in ALDH1high CSC-like cells sorted from A549 lung cancer cells. In APBB1-deficient H460 cells with forced overexpression of APBB1, the protein directly interacted with IGF1Rβ, enhanced phosphorylation of IGF1Rβ/PI3K/AKT pathway(activation) and subsequently induced the phosphorylation of GSK3β(inactivation). This phosphorylation stabilized Snail1, a negative regulator of E-cadherin expression, and regulated β-catenin-mediated ALDH1 expression, which are representative markers for EMT and CSCs, respectively. In contrast, suppression of APBB1 expression with siRNA yielded the opposite effects in APBB1-rich A549 cells. We concluded that APBB1 partly regulates the expression of ALDH1. We also found that APBB1 regulates activation of nuclear factor-κB, which is involved in reducing various stresses including oxidative stress, which suggests that APBB1 is associated with γ-radiation sensitivity. Our findings imply that APBB1 plays an important role in the maintenance of EMT-associated CSC-like properties and γ-radiation resistance via activation of IGF1Rβ/AKT/GSK3β pathway in lung cancer cells, highlighting APBB1 as a potential target for therapeutic cancer treatment. 

     

    Author information

    Lee JH1, Kim JY1, Kim SY2, Choi SI2, Kim KC2, Cho EW3, Kim IG4.

    1Department of Radiation Biology, Environmental Radiation Research Group, Korea Atomic Energy Research Institute, 111, Daedeok-Daero 989 Beon-Gil, Yuseong-Gu, Daejeon, South Korea; Department of Radiation Biotechnology and Applied Radioisotope, Korea University of Science and Technology (UST), 989-111 Daedeok-Daero, Yuseong-Gu, Daejeon 305-353, South Korea.

    2Department of Radiation Biology, Environmental Radiation Research Group, Korea Atomic Energy Research Institute, 111, Daedeok-Daero 989 Beon-Gil, Yuseong-Gu, Daejeon, South Korea.

    3Rare Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, 25 Gwahak-ro, Yuseong-gu, Daejeon 34141, South Korea.

    4Department of Radiation Biology, Environmental Radiation Research Group, Korea Atomic Energy Research Institute, 111, Daedeok-Daero 989 Beon-Gil, Yuseong-Gu, Daejeon, South Korea; Department of Radiation Biotechnology and Applied Radioisotope, Korea University of Science and Technology (UST), 989-111 Daedeok-Daero, Yuseong-Gu, Daejeon 305-353, South Korea. Electronic address: igkim@kaeri.re.kr. 

  • 키워드
    ALDH1; APBB1; Cancer stem cell; EMT; IGF1R
  • 덧글달기
    덧글달기
       IP : 18.118.226.105

    등록