Role and molecular mechanism of stem cells in colorectal cancer initiation

被引:24
作者
Wang, Meng-Yan [1 ]
Qiu, Yu-Han [1 ]
Cai, Mei-Lian [1 ]
Zhang, Cong-Hui [1 ]
Wang, Xiao-Wei [1 ]
Liu, Hong [1 ]
Yi-Chen [2 ]
Zhao, Wu-Li [1 ]
Liu, Jing-Bo [3 ]
Shao, Rong-Guang [1 ]
机构
[1] Peking Union Med Coll & Chinese Acad Med Sci, Inst Med Biotechnol, Key Lab Antibiot Bioengn, Minist Hlth,Lab Oncol, Beijing, Peoples R China
[2] Southwest Univ, Coll Pharmaceut Sci & Chinese Med, Chongqing, Peoples R China
[3] Beijing Univ Chinese Med, Dept Urol, Dongzhimen Hosp, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorectal cancer; cancer stem cells; cancer recurrence and metastasis; Wnt pathway; drug resistance; molecular mechanism; chemotherapy; DRUG-RESISTANCE; SELF-RENEWAL; TUMOR; COLON; MARKER; INTESTINE; PATHWAYS; AGENTS; DCLK1; EPCAM;
D O I
10.1080/1061186X.2019.1632317
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent years, the rate of colorectal cancer has sharply increased, especially in China, where it ranks second for the number of cancer fatalities. Currently, the treatment of colorectal cancer patients involves the combination of resection surgery and treatment with postoperative anticancer drugs such as 5-FU and oxaliplatin. However, recurrence and metastasis after treatment are still the dominant reasons for the low survival rate. Colorectal cancer stem cells (CSCs) are regarded as the key contributors to tumour recurrence and metastasis due to their resistance to chemotherapy drugs and their extremely high tumourigenicity. Once CSCs overcome chemotherapy treatment, they continue to survive and reinitiate proliferation to form tumours, leading to recurrence. The dominant reason for CSC resistance is that most anticancer drugs are aimed at inhibiting proliferative pathways in cancer cells that differ from those in CSCs. Therefore, studies on the characteristics of CSCs and their intracellular molecular pathways are essential for the exploration of CSC-targeted drugs. In this report, we review recent advances in the research of CSCs and, in particular, review the important intracellular molecular pathways, such as HOXA5-catenin, STRAP-NOTCH and YAP/TAZ, related to the maintenance and differentiation of stem cells to generate a theoretical basis for the exploration of CSC-targeted drugs.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 75 条
[11]   Analysis of the clinical significance of DCLK1+ colorectal cancer using novel monoclonal antibodies against DCLK1 [J].
Dai, Tianqi ;
Hu, Yunlong ;
Lv, Fulian ;
Ozawa, Tatsuhiko ;
Sun, Xin ;
Huang, Jingjing ;
Han, Xiaojian ;
Kishi, Hiroyuki ;
Muraguchi, Atsushi ;
Jin, Aishun .
ONCOTARGETS AND THERAPY, 2018, 11 :5047-5057
[12]   Phenotypic characterization of human colorectal cancer stem cells [J].
Dalerba, Piero ;
Dylla, Scott J. ;
Park, In-Kyung ;
Liu, Rui ;
Wang, Xinhao ;
Cho, Robert W. ;
Hoey, Timothy ;
Gurney, Austin ;
Huang, Emina H. ;
Simeone, Diane M. ;
Shelton, Andrew A. ;
Parmiani, Giorgio ;
Castelli, Chiara ;
Clarke, Michael F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (24) :10158-10163
[13]   Stem cell concepts renew cancer research [J].
Dick, John E. .
BLOOD, 2008, 112 (13) :4793-4807
[14]   Distinct Types of Tumor-Initiating Cells Form Human Colon Cancer Tumors and Metastases [J].
Dieter, Sebastian M. ;
Ball, Claudia R. ;
Hoffmann, Christopher M. ;
Nowrouzi, Ali ;
Herbst, Friederike ;
Zavidij, Oksana ;
Abel, Ulrich ;
Arens, Anne ;
Weichert, Wilko ;
Brand, Karsten ;
Koch, Moritz ;
Weitz, Juergen ;
Schmidt, Manfred ;
von Kalle, Christof ;
Glimm, Hanno .
CELL STEM CELL, 2011, 9 (04) :357-365
[15]   A Two-Dimensional Model of the Colonic Crypt Accounting for the Role of the Basement Membrane and Pericryptal Fibroblast Sheath [J].
Dunn, Sara-Jane ;
Appleton, Paul L. ;
Nelson, Scott A. ;
Naethke, Inke S. ;
Gavaghan, David J. ;
Osborne, James M. .
PLOS COMPUTATIONAL BIOLOGY, 2012, 8 (05)
[16]   IL33 Promotes Colon Cancer Cell Stemness via JNK Activation and Macrophage Recruitment [J].
Fang, Min ;
Li, Yongkui ;
Huang, Kai ;
Qi, Shanshan ;
Zhang, Jian ;
Zgodzinski, Witold ;
Majewski, Marek ;
Wallner, Grzegorz ;
Gozdz, Stanislaw ;
Macek, Pawel ;
Kowalik, Artur ;
Pasiarski, Marcin ;
Grywalska, Ewelina ;
Vatan, Linda ;
Nagarsheth, Nisha ;
Li, Wei ;
Zhao, Lili ;
Kryczek, Ilona ;
Wang, Guobin ;
Wang, Zheng ;
Zou, Weiping ;
Wang, Lin .
CANCER RESEARCH, 2017, 77 (10) :2735-2745
[17]   Isolation and characterization of tumorigenic, stem-like neural precursors from human glioblastoma [J].
Galli, R ;
Binda, E ;
Orfanelli, U ;
Cipelletti, B ;
Gritti, A ;
De Vitis, S ;
Fiocco, R ;
Foroni, C ;
Dimeco, F ;
Vescovi, A .
CANCER RESEARCH, 2004, 64 (19) :7011-7021
[18]   High-throughput metabolomics for discovering metabolic biomarkers from intestinal tumorigenesis in APC min/+ mice based on liquid chromatography/mass spectrometry [J].
Guo, Xiang-dong ;
Liu, Lei ;
Xiao, Han-yan .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2018, 1100 :131-139
[19]   Distinct populations of cancer stem cells determine tumor growth and metastatic activity in human pancreatic cancer [J].
Hermann, Patrick C. ;
Huber, Stephan L. ;
Herrler, Tanja ;
Aicher, Alexandra ;
Ellwart, Joachim W. ;
Guba, Markus ;
Bruns, Christiane J. ;
Heeschen, Christopher .
CELL STEM CELL, 2007, 1 (03) :313-323
[20]   Hypoxia-Induced Downregulation of DUSP-2 Phosphatase Drives Colon Cancer Stemness [J].
Hou, Pei-Chi ;
Li, Yo-Hua ;
Lin, Shih-Chieh ;
Lin, Shau-Chieh ;
Lee, Jenq-Chang ;
Lin, Bo-Wen ;
Liou, Jing-Ping ;
Chang, Jang-Yang ;
Kuo, Ching-Chuan ;
Liu, Yi-Min ;
Sun, H. Sunny ;
Tsai, Shaw-Jenq .
CANCER RESEARCH, 2017, 77 (16) :4305-4316