Targeting Cancer Stem Cells for Chemoprevention of Pancreatic Cancer

被引:55
作者
Subramaniam, Dharmalingam [1 ,2 ]
Kaushik, Gaurav [1 ]
Dandawate, Prasad [1 ]
Anant, Shrikant [1 ,2 ]
机构
[1] Univ Kansas, Med Ctr, Dept Surg, Kansas City, KS 66160 USA
[2] Univ Kansas, Med Ctr, Ctr Canc, Kansas City, KS 66160 USA
基金
美国国家卫生研究院;
关键词
Cancer stem cells; signaling; DCLK1; natural compounds; chemoprevention; pancreatic cancer; EPITHELIAL-MESENCHYMAL TRANSITION; HEDGEHOG SIGNALING PATHWAY; DOWN-REGULATION; SELF-RENEWAL; IN-VITRO; GROWTH; INHIBITION; NOTCH; PROLIFERATION; GEMCITABINE;
D O I
10.2174/0929867324666170127095832
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pancreatic ductal adenocarcinoma is one of the deadliest cancers worldwide and the fourth leading cause of cancer-related deaths in United States. Regardless of the advances in molecular pathogenesis and consequential efforts to suppress the disease, this cancer remains a major health problem in United States. By 2030, the projection is that pancreatic cancer will be climb up to be the second leading cause of cancer-related deaths in the United States. Pancreatic cancer is a rapidly invasive and highly metastatic cancer, and does not respond to standard therapies. Emerging evidence supports that the presence of a unique population of cells called cancer stem cells (CSCs) as potential cancer inducing cells and efforts are underway to develop therapeutic strategies targeting these cells. CSCs are rare quiescent cells, and with the capacity to self-renew through asymmetric/symmetric cell division, as well as differentiate into various lineages of cells in the cancer. Studies have been shown that CSCs are highly resistant to standard therapy and also responsible for drug resistance, cancer recurrence and metastasis. To overcome this problem, we need novel preventive agents that target these CSCs. Natural compounds or phytochemicals have ability to target these CSCs and their signaling pathways. Therefore, in the present review article, we summarize our current understanding of pancreatic CSCs and their signaling pathways, and the phytochemicals that target these cells including curcumin, resveratrol, tea polyphenol EGCG (epigallocatechin-3-gallate), crocetinic acid, sulforaphane, genistein, indole-3-carbinol, vitamin E dtocotrienol, Plumbagin, quercetin, triptolide, Licofelene and Quinomycin. These natural compounds or phytochemicals, which inhibit cancer stem cells may prove to be promising agents for the prevention and treatment of pancreatic cancers.
引用
收藏
页码:2585 / 2594
页数:10
相关论文
共 101 条
[1]   Identification of Pancreatic Cancer Stem Cells and Selective Toxicity of Chemotherapeutic Agents [J].
Adikrisna, Rama ;
Tanaka, Shinji ;
Muramatsu, Shunsuke ;
Aihara, Arihiro ;
Ban, Daisuke ;
Ochiai, Takanori ;
Irie, Takumi ;
Kudo, Atsushi ;
Nakamura, Noriaki ;
Yamaoka, Shoji ;
Arii, Shigeki .
GASTROENTEROLOGY, 2012, 143 (01) :234-U448
[2]  
Aggarwal BB, 2004, ANTICANCER RES, V24, P2783
[3]   Notch signaling in cancer [J].
Allenspach, EJ ;
Maillard, I ;
Aster, JC ;
Pear, WS .
CANCER BIOLOGY & THERAPY, 2002, 1 (05) :466-476
[4]  
Bai CB, 2002, DEVELOPMENT, V129, P4753
[5]   DCLK1 Marks a Morphologically Distinct Subpopulation of Cells With Stem Cell Properties in Preinvasive Pancreatic Cancer [J].
Bailey, Jennifer M. ;
Alsina, Janivette ;
Rasheed, Zeshaan A. ;
McAllister, Florencia M. ;
Fu, Ya-Yuan ;
Plentz, Ruben ;
Zhang, Hao ;
Pasricha, Pankaj J. ;
Bardeesy, Nabeel ;
Matsui, William ;
Maitra, Anirban ;
Leach, Steven D. .
GASTROENTEROLOGY, 2014, 146 (01) :245-256
[6]   Assessing clinical benefit in the treatment of pancreas cancer: Gemcitabine compared to 5-fluorouracil [J].
Burris, H ;
Storniolo, AM .
EUROPEAN JOURNAL OF CANCER, 1997, 33 :S18-S22
[7]   Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: A randomized trial [J].
Burris, HA ;
Moore, MJ ;
Andersen, J ;
Green, MR ;
Rothenberg, ML ;
Madiano, MR ;
Cripps, MC ;
Portenoy, RK ;
Storniolo, AM ;
Tarassoff, P ;
Nelson, R ;
Dorr, FA ;
Stephens, CD ;
VanHoff, DD .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) :2403-2413
[8]   K-Ras promotes growth transformation and invasion of immortalized human pancreatic cells by Raf and phosphatidylinositol 3-kinase signaling [J].
Campbell, Paul M. ;
Groehler, Angela L. ;
Lee, Kwang M. ;
Ouellette, Michel M. ;
Khazak, Vladimir ;
Der, Channing J. .
CANCER RESEARCH, 2007, 67 (05) :2098-2106
[9]   Curcumin inhibits hypoxia-induced epithelial-mesenchymal transition in pancreatic cancer cells via suppression of the hedgehog signaling pathway [J].
Cao, Lei ;
Xiao, Xue ;
Lei, Jianjun ;
Duan, Wanxing ;
Ma, Qingyong ;
Li, Wei .
ONCOLOGY REPORTS, 2016, 35 (06) :3728-3734
[10]   Metformin Increases Sensitivity of Pancreatic Cancer Cells to Gemcitabine by Reducing CD133+ Cell Populations and Suppressing ERK/P70S6K Signaling [J].
Chai, Xinqun ;
Chu, Hongpeng ;
Yang, Xuan ;
Meng, Yuanpu ;
Shi, Pengfei ;
Gou, Shanmiao .
SCIENTIFIC REPORTS, 2015, 5