Nanobiopolymer for Direct Targeting and Inhibition of EGFR Expression in Triple Negative Breast Cancer

被引:46
|
作者
Inoue, Satoshi [1 ]
Patil, Rameshwar [1 ]
Portilla-Arias, Jose [1 ]
Ding, Hui [1 ]
Konda, Bindu [1 ]
Espinoza, Andres [1 ]
Mongayt, Dmitriy [2 ]
Markman, Janet L. [1 ]
Elramsisy, Adam [1 ]
Phillips, H. Westley [1 ]
Black, Keith L. [1 ]
Holler, Eggehard [1 ]
Ljubimova, Julia Y. [1 ]
机构
[1] Cedars Sinai Med Ctr, Dept Neurosurg, Los Angeles, CA 90048 USA
[2] Northeastern Univ, Ctr Pharmaceut Biotechnol & Nanomed, Boston, MA 02115 USA
来源
PLOS ONE | 2012年 / 7卷 / 02期
基金
美国国家卫生研究院;
关键词
GROWTH-FACTOR RECEPTOR; TUMOR-CELLS; POLYMALIC ACID; IN-VITRO; ANTIBODY; ANTISENSE; LIPOSOMES; DELIVERY; TRANSFERRIN; APOPTOSIS;
D O I
10.1371/journal.pone.0031070
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Treatment options for triple negative breast cancer (TNBC) are generally limited to cytotoxic chemotherapy. Recently, anti-epidermal growth factor receptor (EGFR) therapy has been introduced for TNBC patients. We engineered a novel nanobioconjugate based on a poly(beta-L-malic acid) (PMLA) nanoplatform for TNBC treatment. The nanobioconjugate carries anti-tumor nucleosome-specific monoclonal antibody (mAb) 2C5 to target breast cancer cells, anti-mouse transferrin receptor (TfR) antibody for drug delivery through the host endothelial system, and Morpholino antisense oligonucleotide (AON) to inhibit EGFR synthesis. The nanobioconjugates variants were: (1) P (BioPolymer) with AON, 2C5 and anti-TfR for tumor endothelial and cancer cell targeting, and EGFR suppression (P/AON/2C5/TfR), and (2) P with AON and 2C5 (P/AON/2C5). Controls included (3) P with 2C5 but without AON (P/2C5), (4) PBS, and (5) P with PEG and leucine ester (LOEt) for endosomal escape (P/mPEG/LOEt). Drugs were injected intravenously to MDA-MB-468 TNBC bearing mice. Tissue accumulation of injected nanobioconjugates labeled with Alexa Fluor 680 was examined by Xenogen IVIS 200 (live imaging) and confocal microscopy of tissue sections. Levels of EGFR, phosphorylated and total Akt in tumor samples were detected by western blotting. In vitro western blot showed that the leading nanobioconjugate P/AON/2C5/TfR inhibited EGFR synthesis significantly better than naked AON. In vivo imaging revealed that 2C5 increased drug-tumor accumulation. Significant tumor growth inhibition was observed in mice treated with the lead nanobioconjugate (1) [P = 0.03 vs. controls; P<0.05 vs. nanobioconjugate variant (2)]. Lead nanobioconjugate (1) also showed stronger inhibition of EGFR expression and Akt phosphorylation than other treatments. Treatment of TNBC with the new nanobioconjugate results in tumor growth arrest by inhibiting EGFR and its downstream signaling intermediate, phosphorylated Akt. The nanobioconjugate represents a new generation of nanodrugs for treatment of TNBC.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] Radioimmunoimaging of EGFR with pretargeting Cetuximab in triple negative breast cancer
    Lan, X.
    Yuan, L.
    Gai, Y.
    An, R.
    Zhang, Y.
    EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2019, 46 (SUPPL 1) : S746 - S746
  • [32] EGFR and MEK Blockade in Triple Negative Breast Cancer Cells
    Maiello, Monica Rosaria
    D'Alessio, Amelia
    Bevilacqua, Simona
    Gallo, Marianna
    Normanno, Nicola
    De Luca, Antonella
    JOURNAL OF CELLULAR BIOCHEMISTRY, 2015, 116 (12) : 2778 - 2785
  • [33] Synergistic inhibition of thioridazine combined with carboplatin on triple negative breast cancer by targeting cancer stem cells
    Wang, Yi
    Xia, Leiming
    Gong, Li
    Xia, Yang
    Liu, Liu
    Liu, Yuanyuan
    Max, Wicha
    Chang, Alfred E.
    Li, Qiao
    Bao, Yangyi
    CANCER RESEARCH, 2020, 80 (16)
  • [34] Raloxifene reduces triple-negative breast cancer tumor growth and decreases EGFR expression
    Taurin, Sebastien
    Allen, Kirstie M.
    Scandlyn, Marissa J.
    Rosengren, Rhonda J.
    INTERNATIONAL JOURNAL OF ONCOLOGY, 2013, 43 (03) : 785 - 792
  • [35] Protein expression, gene amplification, and mutational analysis of EGFR in triple-negative breast cancer
    Hiroki Nakajima
    Yuko Ishikawa
    Mio Furuya
    Takaaki Sano
    Yoshihiro Ohno
    Jun Horiguchi
    Tetsunari Oyama
    Breast Cancer, 2014, 21 : 66 - 74
  • [36] Protein expression, gene amplification, and mutational analysis of EGFR in triple-negative breast cancer
    Nakajima, Hiroki
    Ishikawa, Yuko
    Furuya, Mio
    Sano, Takaaki
    Ohno, Yoshihiro
    Horiguchi, Jun
    Oyama, Tetsunari
    BREAST CANCER, 2014, 21 (01) : 66 - 74
  • [37] EGFR is transferred from triple negative breast cancer cells to immune cells via trogocytosis and expression of EGFR on immune cells is associated with high tumor grade of triple negative breast cancer patients
    Suzuki, Eiji
    Yamaguchi, Ayane
    Kataoka, Tatsuki R.
    Hirata, Masahiro
    Kawaguchi, Kosuke
    Nishie, Mariko
    Toi, Masakazu
    CANCER RESEARCH, 2015, 75
  • [38] Targeting MET and EGFR crosstalk signaling in triple-negative breast cancers
    Linklater, Erik S.
    Tovar, Elizabeth A.
    Essenburg, Curt J.
    Turner, Lisa
    Madaj, Zachary
    Winn, Mary E.
    Melnik, Marianne K.
    Korkaya, Hasan
    Maroun, Christiane R.
    Christensen, James G.
    Steensma, Matthew R.
    Boerner, Julie L.
    Graveel, Carrie R.
    ONCOTARGET, 2016, 7 (43) : 69903 - 69915
  • [39] Targeting stem cells in triple negative breast cancer through combined MEK and AKT inhibition
    Zhang, Kevin
    McDermott, Sean P.
    Wicha, Max S.
    CANCER RESEARCH, 2014, 74 (19)
  • [40] TBCRC 001: EGFR inhibition with cetuximab in metastatic triple negative (basal-like) breast cancer
    Carey, L. A.
    Mayer, E.
    Marcom, P. K.
    Rugo, H.
    Liu, M.
    Ma, C.
    Rimawi, M.
    Storniolo, A.
    Forero, A.
    Esteva, F.
    Wolff, A.
    Ingle, J.
    Ferraro, M.
    Sawyer, L.
    Davidson, N.
    Perou, C. M.
    Winer, E. P.
    BREAST CANCER RESEARCH AND TREATMENT, 2007, 106 : S32 - S32