Targeting cancer stem cell-specific markers and/or associated signaling pathways for overcoming cancer drug resistance

被引:26
作者
Ranji, Peyman [1 ]
Kesejini, Tayyebali Salmani [1 ]
Saeedikhoo, Sara [1 ]
Alizadeh, Ali Mohammad [1 ]
机构
[1] Univ Tehran Med Sci, Canc Res Ctr, Tehran, Iran
关键词
Cancer stem cell; Drug resistance; Nanotechnology; Gene therapy; Immunotherapy; Review; TRANS-RETINOIC ACID; KINASE RECEPTOR INHIBITOR; ACUTE MYELOID-LEUKEMIA; MULTIDRUG-RESISTANCE; IN-VIVO; MONOCLONAL-ANTIBODY; TYROSINE-KINASE; SMALL-MOLECULE; THERAPEUTIC TARGETS; COLORECTAL-CANCER;
D O I
10.1007/s13277-016-5294-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer stem cells (CSCs) are a small subpopulation of tumor cells with capabilities of self-renewal, dedifferentiation, tumorigenicity, and inherent chemo-and-radio therapy resistance. Tumor resistance is believed to be caused by CSCs that are intrinsically challenging to common treatments. A number of CSC markers including CD44, CD133, receptor tyrosine kinase, aldehyde dehydrogenases, epithelial cell adhesion molecule/epithelial specific antigen, and ATP-binding cassette subfamily G member 2 have been proved as the useful targets for defining CSC population in solid tumors. Furthermore, targeting CSC markers through new therapeutic strategies will ultimately improve treatments and overcome cancer drug resistance. Therefore, the identification of novel strategies to increase sensitivity of CSC markers has major clinical implications. This review will focus on the innovative treatment methods such as nano-, immuno-, gene-, and chemotherapy approaches for targeting CSC-specific markers and/or their associated signaling pathways.
引用
收藏
页码:13059 / 13075
页数:17
相关论文
共 125 条
  • [1] Overcoming Challenges of Ovarian Cancer Stem Cells: Novel Therapeutic Approaches
    Aguilar-Gallardo, Cristobal
    Cecilia Rutledge, Emily
    Martinez-Arroyo, Ana M.
    Jose Hidalgo, Juan
    Domingo, Santiago
    Simon, Carlos
    [J]. STEM CELL REVIEWS AND REPORTS, 2012, 8 (03) : 994 - 1010
  • [2] Koenimbin, a natural dietary compound of Murraya koenigii (L) Spreng: inhibition of MCF7 breast cancer cells and targeting of derived MCF7 breast cancer stem cells (CD44+/CD24-/low): an in vitro study
    Ahmadipour, Fatemeh
    Noordin, Mohamed Ibrahim
    Mohan, Syam
    Arya, Aditya
    Paydar, Mohammadjavad
    Looi, Chung Yeng
    Keong, Yeap Swee
    Siyamak, Ebrahimi Nigjeh
    Fani, Somayeh
    Firoozi, Maryam
    Yong, Chung Lip
    Sukari, Mohamed Aspollah
    Kamalidehghan, Behnam
    [J]. DRUG DESIGN DEVELOPMENT AND THERAPY, 2015, 9 : 1193 - 1208
  • [3] Targeting cancer-initiating cell drug-resistance: a roadmap to a new-generation of cancer therapies?
    Alama, Angela
    Orengo, Anna Maria
    Ferrini, Silvano
    Gangemi, Rosaria
    [J]. DRUG DISCOVERY TODAY, 2012, 17 (9-10) : 435 - 442
  • [4] Metastasis review: from bench to bedside
    Alizadeh, Ali Mohammad
    Shiri, Sadaf
    Farsinejad, Sadaf
    [J]. TUMOR BIOLOGY, 2014, 35 (09) : 8483 - 8523
  • [5] Salinomycin possesses anti-tumor activity and inhibits breast cancer stem-like cells via an apoptosis-independent pathway
    An, Hyunsook
    Kim, Ji Young
    Lee, Nahyun
    Cho, Youngkwan
    Oh, Eunhye
    Seo, Jae Hong
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2015, 466 (04) : 696 - 703
  • [6] Role of platelet-derived growth factors in physiology and medicine
    Andrae, Johanna
    Gallini, Radiosa
    Betsholtz, Christer
    [J]. GENES & DEVELOPMENT, 2008, 22 (10) : 1276 - 1312
  • [7] Cell surface markers of cancer stem cells: diagnostic macromolecules and targets for drug delivery
    Andrews, Timothy E.
    Wang, Dan
    Harki, Daniel A.
    [J]. DRUG DELIVERY AND TRANSLATIONAL RESEARCH, 2013, 3 (02) : 121 - 142
  • [8] [Anonymous], 2015, SCI REP
  • [9] Targeting MET for glioma therapy
    Awad, Ahmed J.
    Burns, Terry C.
    Zhang, Ying
    Abounader, Roger
    [J]. NEUROSURGICAL FOCUS, 2014, 37 (06)
  • [10] EpCAM (CD326) finding its role in cancer
    Baeuerle, P. A.
    Gires, O.
    [J]. BRITISH JOURNAL OF CANCER, 2007, 96 (03) : 417 - 423