Lapatinib as a Chemotherapeutic Drug

被引:2
|
作者
Obajimi, Oluwakemi [1 ,2 ]
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med, Camden, NJ 08103 USA
[2] Cooper Univ Hosp, Cooper Canc Inst, Camden, NJ 08103 USA
关键词
ErbB1; EGFR; ErbB2; HER-2; lapatinib; GW572016; cancer treatment; PI3K; Akt; MAPK; capecitabine; trastuzumab; tamoxifen; combination therapy; monotherapy; EPIDERMAL-GROWTH-FACTOR; TYROSINE-KINASE-INHIBITOR; FACTOR RECEPTOR EXPRESSION; ERBB SIGNALING NETWORK; BREAST-CANCER; PHASE-II; GENE AMPLIFICATION; BRAIN METASTASES; DUAL INHIBITOR; MAP KINASE;
D O I
10.2174/157489209789206896
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human epidermal growth factor receptor (HER) signaling is frequently associated with the development and progression of several types of cancers. Both the MAPK and the PI3K/Akt pathways have been implicated as effectors of HER signaling by promoting anti-apoptotic and pro-proliferative effects in cancer cells. As a result, many anti-HER drugs have been developed and patented for use in cancer therapy. One such drug that was recently approved for clinical trials is lapatinib (Tykerb, GW572016). Lapatinib is a small molecule inhibitor that is active at the ATP binding site of the tyrosine kinase involved in HER signaling. Importantly, this drug has dual specificity acting at the ATP binding sites of both HER-2 and HER-1 (EGFR). This review therefore summarizes the current knowledge based on pre-clinical and clinical evidence of the therapeutic effects of lapatinib against cancer and the promising strategy of combination therapy with the possibility of circumventing the problems of drug resistance commonly faced by chemotherapeutic drugs.
引用
收藏
页码:216 / 226
页数:11
相关论文
共 50 条
  • [1] Lapatinib promotes the incidence of hepatotoxicity by increasing chemotherapeutic agent accumulation in hepatocytes
    Dai, ChunLing
    Ma, ShaoLin
    Wang, Fang
    Zhao, HongYun
    Wu, XingPing
    Huang, ZhenCong
    Chen, ZheSheng
    To, Kenneth
    Fu, LiWu
    ONCOTARGET, 2015, 6 (19) : 17738 - 17752
  • [2] Tosylate salts of the anticancer drug lapatinib
    Ravikumar, K.
    Sridhar, B.
    Nanubolu, Jagadeesh Babu
    Rao, A. K. S. Bhujanga
    Jyothiprasad, R.
    ACTA CRYSTALLOGRAPHICA SECTION C-STRUCTURAL CHEMISTRY, 2013, 69 : 1516 - +
  • [3] Lapatinib promotes promoted the incidence of hepatotoxicity by increasing chemotherapeutic agent accumulation in hepatocytes
    Dai, Chunling
    Ma, Shaolin
    Chen, Zhesheng
    To, Kenneth
    Fu, Liwu
    CANCER RESEARCH, 2015, 75
  • [4] CHEMOTHERAPEUTIC DRUG DEVELOPMENT AT SKI
    HADDEN, JW
    CLINICAL BULLETIN, 1977, 7 (04) : 160 - 163
  • [5] NEW ANTIVIRAL CHEMOTHERAPEUTIC DRUG RIODOXOL
    GRINEV, AV
    PERSHIN, GN
    STEBAEVA, LF
    NIKOLAEVA, IS
    SHVEDOV, VI
    KHARIZOMENOVA, IA
    BOTKINA, EM
    KHIMIKO-FARMATSEVTICHESKII ZHURNAL, 1984, 18 (03): : 374 - 376
  • [6] PEGylated nanodiamond for chemotherapeutic drug delivery
    Wang, Dongxin
    Tong, Yaoli
    Li, Yingqi
    Tian, Zhimei
    Cao, Ruixia
    Yang, Binsheng
    DIAMOND AND RELATED MATERIALS, 2013, 36 : 26 - 34
  • [7] Multiphysics and Multiscale Analysis for Chemotherapeutic Drug
    Zhang, Linan
    Kim, Sung Youb
    Kim, Dongchoul
    BIOMED RESEARCH INTERNATIONAL, 2015, 2015
  • [8] The Hippo pathway in chemotherapeutic drug resistance
    Zhao, Yulei
    Yang, Xiaolong
    INTERNATIONAL JOURNAL OF CANCER, 2015, 137 (12) : 2767 - 2773
  • [9] Physicochemical Characterization and Cyclodextrin Complexation of the Anticancer Drug Lapatinib
    Toth, Gergo
    Janoska, Adam
    Voelgyi, Gergely
    Szabo, Zoltan-Istvan
    Orgovan, Gabor
    Mirzahosseini, Arash
    Noszal, Bela
    JOURNAL OF CHEMISTRY, 2017, 2017
  • [10] STRATEGY AND TACTICS OF CHEMOTHERAPEUTIC DRUG DEVELOPMENT
    HAHN, FE
    NATURWISSENSCHAFTEN, 1975, 62 (10) : 449 - 458