Metuzumab enhanced chemosensitivity and apoptosis in non-small cell lung carcinoma

被引:19
|
作者
Feng, Fei [1 ]
Wang, Bin [1 ]
Sun, Xiuxuan [1 ]
Zhu, Yumeng [1 ]
Tang, Hao [2 ]
Nan, Gang [1 ]
Wang, Lijuan [1 ]
Wu, Bo [1 ]
Huhe, Muren [1 ]
Liu, Shuangshuang [1 ]
Diao, Tengyue [1 ]
Hou, Rong [1 ]
Zhang, Yang [1 ]
Zhang, Zheng [1 ]
机构
[1] Fourth Mil Med Univ, Natl Translat Sci Ctr Mol Med, Dept Cell Biol, Xian 710032, Peoples R China
[2] Pacific Meinuoke Biopharmaceut Co, Changzhou, Peoples R China
关键词
CD147; chemosensitivity; gemcitabine; metuzumab; monoclonal antibody; non-small-cell lung cancer; targeted therapy; SIGNALING PATHWAY; POOR-PROGNOSIS; IN-VITRO; CANCER; GEMCITABINE; EXPRESSION; CD147; RESISTANCE; OVEREXPRESSION; ADENOCARCINOMA;
D O I
10.1080/15384047.2016.1276126
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Targeted therapeutics is used as an alternative treatment of non-small cell lung cancer (NSCLC); however, treatment effect is far from being satisfactory, and therefore identification of new targets is needed. We have previously shown that metuzumab inhibit tumor growth in vivo. The present study was performed to investigate the anti-tumor efficacy of metuzumab combined with gemcitabine and cisplatin (GP), paclitaxel and cisplatin (TP) or navelbine and cisplatin (NP) regimens in multiple NSCLC cell lines. Our results demonstrate that, in comparison to single agent metuzumab or GP treated cells, metuzumab combined with GP display inhibitory effects on tumor growth. Furthermore, we found that metuzumab elevated the sensitivity of cell lines to gemcitabine, which was identified by MTT assay. Flow cytometric analysis showed that metuzumab combined with gemcitabine (GEM) treatment led to an obvious G1 arrest and an elevated apoptosis in A549, NCI-H460 and NCI-H520 cells. Western blot analysis also demonstrated a significantly reduced level of cyclin D1, Bcl-2, and an obviously increase level of Bax and full-length caspase-3 in A549, NCI-H460 and NCI-H520 cells treated with metuzumab/gemcitabine combination in comparison with single agent treated cells. In addition, metuzumab/gemcitabine treated A549, NCI-H460 and NCI-H520 cells also demonstrated a significantly increase in deoxycytidine kinase (dCK) protein level compared with single agent metuzumab or gemcitabine treated cells. Xenograft models also demonstrated that this metuzumab/gemcitabine combination led to upregulation of dCK. Taken together, the mechanisms of metuzumab combined with GP repress tumor growth were that the combined treatment significantly inhibited the tumor cell proliferation, apoptosis and cell cycle in vitro and in vivo and at least partially by induction of dCK expression. Our results suggested that metuzumab could significantly enhance chemosensitivity of human NSCLC cells to gemcitabine. Metuzumab/gemcitabine combination treatment may be a potentially useful therapeutic regimen for NSCLC patients.
引用
收藏
页码:51 / 62
页数:12
相关论文
共 50 条
  • [1] Clinical potential of necitumumab in non-small cell lung carcinoma
    Genova, Carlo
    Hirsch, Fred R.
    ONCOTARGETS AND THERAPY, 2016, 9 : 5427 - 5437
  • [2] Thymidylate synthase and dihydrofolate reductase expression in non-small cell lung carcinoma: The association with treatment efficacy of pemetrexed
    Chen, Chung-Yu
    Chang, Yih-Leong
    Shih, Jin-Yuan
    Lin, Jou-Wei
    Chen, Kuan-Yu
    Yang, Chih-Hsin
    Yu, Chong-Jen
    Yang, Pan-Chyr
    LUNG CANCER, 2011, 74 (01) : 132 - 138
  • [3] Associations Between Driver Gene Mutations and Cytotoxic Chemosensitivity in Patients with Non-small Cell Lung Cancer
    Morodomi, Yosuke
    Okamoto, Tatsuro
    Kohno, Mikihiro
    Katsura, Masakazu
    Takada, Kazuki
    Suzuki, Yuzo
    Fujishita, Takatoshi
    Kitahara, Hirokazu
    Shimamatsu, Shinichiro
    Yoshida, Tsukihisa
    Tagawa, Tetsuzo
    Okano, Shinji
    Maehara, Yoshihiko
    ANTICANCER RESEARCH, 2015, 35 (03) : 1791 - 1796
  • [4] RB protein status and chemosensitivity in non-small cell lung cancers
    Yamamoto, Y
    Shimizu, E
    Masuda, N
    Takada, M
    Sone, S
    ONCOLOGY REPORTS, 1998, 5 (02) : 447 - 451
  • [5] Non-Small Cell Lung Carcinoma: An Overview on Targeted Therapy
    Nascimento, Ana Vanessa
    Bousbaa, Hassan
    Ferreira, Domingos
    Sarmento, Bruno
    CURRENT DRUG TARGETS, 2015, 16 (13) : 1448 - 1463
  • [6] Role of circulating microRNAs in non-small cell lung carcinoma
    Baranwal, Harshita
    Mishra, Shravan K.
    Kumari, Niraj
    Singh, Shalini
    Krishnani, Narendra
    Nath, Alok
    Neyaz, Zafar
    INDIAN JOURNAL OF PATHOLOGY AND MICROBIOLOGY, 2024, 67 (03) : 502 - 509
  • [7] Molecular landscape of non-squamous, non-small cell carcinoma of the lung
    Weiss, Mia C.
    Leukam, Michael J.
    Villaflor, Victoria M.
    TRANSLATIONAL CANCER RESEARCH, 2015, 4 (04) : 423 - 434
  • [8] The effects on cell growth and chemosensitivity by livin RNAi in non-small cell lung cancer
    Yuan, Dong
    Liu, Liqun
    Xu, Huaming
    Gu, Dayong
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2009, 320 (1-2) : 133 - 140
  • [9] Untargeted metabolomics analysis of omeprazole-enhanced chemosensitivity to cisplatin in mice with non-small cell lung cancer
    Gao, Huan
    Song, Yanqing
    Ma, Jie
    Zhai, Jinghui
    Zhang, Yueming
    Qu, Xiaoyu
    CHEMICO-BIOLOGICAL INTERACTIONS, 2022, 360
  • [10] Nanog suppression enhanced the chemosensitivity of human non-small-cell lung cancer cells to Cisplatin and inhibited cell migration
    Najafzadeh, Basira
    Motafakkerazad, Rouhollah
    Najafi, Souzan
    Amini, Mohammad
    Alemohammad, Hajar
    Vasefifar, Parisa
    Baradaran, Behzad
    PATHOLOGY RESEARCH AND PRACTICE, 2022, 233