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
  • [41] Synthetic Lethal Interactions between EGFR and PARP Inhibition in Human Triple Negative Breast Cancer Cells
    Nowsheen, Somaira
    Cooper, Tiffiny
    Stanley, Jennifer A.
    Yang, Eddy S.
    PLOS ONE, 2012, 7 (10):
  • [42] Indirect targeting of MYC and direct targeting in combination with chemotherapies are more effective than direct mono-targeting in triple negative breast cancer
    Mekonnen, Negesse
    Yang, Hobin
    Rajasekaran, Nirmal
    Song, Kyoung
    Choi, Yoon-La
    Shin, Young Kee
    TRANSLATIONAL ONCOLOGY, 2025, 51
  • [43] Significance of EGFR mRNA Expression in Luminal and Triple Negative Breast Tumors
    Darbeheshti, Farzaneh
    Izadi, Pantea
    Razavi, Amir Nader Emami
    Kamali, Fatemeh
    Yekaninejad, Mir Saeed
    Bazzaz, Javad Tavakkoly
    INTERNATIONAL JOURNAL OF CANCER MANAGEMENT, 2018, 11 (02)
  • [44] ELP-dependent expression of MCL1 promotes resistance to EGFR inhibition in triple-negative breast cancer cells
    Cruz-Gordillo, Peter
    Honeywell, Megan E.
    Harper, Nicholas W.
    Leete, Thomas
    Lee, Michael J.
    SCIENCE SIGNALING, 2020, 13 (658)
  • [45] Fatty acid inhibition reduces MYC expression in triple-negative breast cancer
    Sritharan, N.
    Lee, J.
    Goga, A.
    EUROPEAN JOURNAL OF CANCER, 2020, 138 : S108 - S108
  • [46] Targeting Cancer Stem Cells in Triple-Negative Breast Cancer
    Park, So-Yeon
    Choi, Jang-Hyun
    Nam, Jeong-Seok
    CANCERS, 2019, 11 (07)
  • [47] Thioridazine combined with carboplatin results in synergistic inhibition of triple negative breast cancer by targeting cancer stem cells
    Wang, Yi
    Xia, Leiming
    Lin, Jing
    Gong, Li
    Xia, Yang
    Xu, Yang
    Liu, Liu
    Bao, Jian
    Zhang, Congshu
    Chai, Yuqing
    Li, Hongxia
    TRANSLATIONAL ONCOLOGY, 2022, 26
  • [48] Macrophage-targeting immunotherapy for triple negative breast cancer
    Fernandez, Matthew E.
    Fines, Cory B.
    Subul, Fatemah S.
    Alhudaithi, Sulaiman S.
    Bear, Harry D.
    Sweet, Douglas H.
    da Rocha, Sandro R.
    CANCER RESEARCH, 2023, 83 (07)
  • [49] Targeting nuclear export for triple negative breast cancer therapy
    Petrocca, Fabio
    CANCER RESEARCH, 2016, 76
  • [50] Targeting triple-negative breast cancer: A clinical perspective
    Popovic, Lazar S.
    Matovina-Brko, Gorana
    Popovic, Maja
    Punie, Kevin
    Cvetanovic, Ana
    Lambertini, Matteo
    ONCOLOGY RESEARCH, 2023, 31 (03) : 221 - 238