Metformin may function as anti-cancer agent via targeting cancer stem cells: the potential biological significance of tumor-associated miRNAs in breast and pancreatic cancers

被引:76
作者
Bao, Bin [1 ]
Azmi, Asfar S. [1 ]
Ali, Shadan [2 ]
Zaiem, Feras [1 ]
Sarkar, Fazlul H. [1 ,2 ]
机构
[1] Wayne State Univ, Sch Med, Karmanos Canc Inst, Dept Pathol, 740 Hudson Webber Canc Res Ctr,4100 John R St, Detroit, MI 48201 USA
[2] Wayne State Univ, Sch Med, Karmanos Canc Inst, Dept Oncol, Detroit, MI 48201 USA
关键词
Metformin; cancer stem cells (CSCs); microRNAs (miRNAs); breast cancer and pancreatic cancer;
D O I
10.3978/j.issn.2305-5839.2014.06.05
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Metformin is one of the most used diabetic drugs for the management of type II diabetes mellitus (DM) in the world. Increased numbers of epidemiological and clinical studies have provided convincing evidence supporting the role of metformin in the development and progression of a variety of human tumors including breast and pancreatic cancer. Substantial pre-clinical evidence from in vitro and in vivo experimental studies strongly suggests that metformin has an anti-cancer activity mediated through the regulation of several cell signaling pathways including activation of AMP kinase (AMPK), and other direct and indirect mechanisms; however, the detailed mechanism(s) has not yet been fully understood. The concept of cancer stem cells (CSCs) has gained significant attention in recent years due its identification and defining its clinical implications in many different tumors including breast cancer and pancreatic cancer. In this review, we will discuss the protective role of metformin in the development of breast and pancreatic cancers. We will further discuss the role of metformin as an anti-cancer agent, which is in part mediated through targeting CSCs. Finally, we will discuss the potential role of metformin in the modulation of tumor-associated or CSC-associated microRNAs (miRNAs) as part of the novel mechanism of action of metformin in the development and progression of breast and pancreatic cancers.
引用
收藏
页数:16
相关论文
共 145 条
[1]   Prospective identification of tumorigenic breast cancer cells [J].
Al-Hajj, M ;
Wicha, MS ;
Benito-Hernandez, A ;
Morrison, SJ ;
Clarke, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (07) :3983-3988
[2]   RETRACTED: Inactivation of Ink4a/Arf leads to deregulated expression of miRNAs in K-Ras transgenic mouse model of pancreatic cancer (Retracted article. See vol. 231, pg. 2303, 2016) [J].
Ali, Shadan ;
Banerjee, Sanjeev ;
Logna, Farah ;
Bao, Bin ;
Philip, Philip A. ;
Korc, Murray ;
Sarkar, Fazlul H. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2012, 227 (10) :3373-3380
[3]   RETRACTED: Gemcitabine Sensitivity Can Be Induced in Pancreatic Cancer Cells through Modulation of miR-200 and miR-21 Expression by Curcumin or Its Analogue CDF (Retracted article. See vol. 78, pg. 5466, 2018) [J].
Ali, Shadan ;
Ahmad, Aamir ;
Banerjee, Sanjeev ;
Padhye, Subhash ;
Dominiak, Kristin ;
Schaffert, Jacqueline M. ;
Wang, Zhiwei ;
Philip, Philip A. ;
Sarkar, Fazlul H. .
CANCER RESEARCH, 2010, 70 (09) :3606-3617
[4]   Risk Factors of Breast Cancer: A Systematic Review and Meta-Analysis [J].
Anothaisintawee, Thunyarat ;
Wiratkapun, Cholatip ;
Lerdsitthichai, Panuwat ;
Kasamesup, Vijj ;
Wongwaisayawan, Sansanee ;
Srinakarin, Jiraporn ;
Hirunpat, Siriporn ;
Woodtichartpreecha, Piyanoot ;
Boonlikit, Sarawan ;
Teerawattananon, Yot ;
Thakkinstian, Ammarin .
ASIA-PACIFIC JOURNAL OF PUBLIC HEALTH, 2013, 25 (05) :368-387
[5]   Therapeutic Potential of an Anti-diabetic Drug, Metformin: Alteration of miRNA expression in Prostate Cancer Cells [J].
Avci, Cigir Biray ;
Harman, Ece ;
Dodurga, Yavuz ;
Susluer, Sunde Yilmaz ;
Gunduz, Cumhur .
ASIAN PACIFIC JOURNAL OF CANCER PREVENTION, 2013, 14 (02) :765-768
[6]   Drug therapy - Metformin [J].
Bailey, CJ ;
Turner, RC .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 334 (09) :574-579
[7]   The tumor suppressor gene rap1GAP is silenced by miR-101-mediated EZH2 overexpression in invasive squamous cell carcinoma [J].
Banerjee, R. ;
Mani, R-S ;
Russo, N. ;
Scanlon, C. S. ;
Tsodikov, A. ;
Jing, X. ;
Cao, Q. ;
Palanisamy, N. ;
Metwally, T. ;
Inglehart, R. C. ;
Tomlins, S. ;
Bradford, C. ;
Carey, T. ;
Wolf, G. ;
Kalyana-Sundaram, S. ;
Chinnaiyan, A. M. ;
Varambally, S. ;
D'Silva, N. J. .
ONCOGENE, 2011, 30 (42) :4339-4349
[8]  
Bao Bin, 2013, Curr Protoc Pharmacol, VChapter 14, DOI 10.1002/0471141755.ph1425s61
[9]   Hypoxia-Induced Aggressiveness of Pancreatic Cancer Cells Is Due to Increased Expression of VEGF, IL-6 and miR-21, Which Can Be Attenuated by CDF Treatment [J].
Bao, Bin ;
Ali, Shadan ;
Ahmad, Aamir ;
Azmi, Asfar S. ;
Li, Yiwei ;
Banerjee, Sanjeev ;
Kong, Dejuan ;
Sethi, Seema ;
Aboukameel, Amro ;
Padhye, Subhash B. ;
Sarkar, Fazlul H. .
PLOS ONE, 2012, 7 (12)
[10]   Hypoxia Induced Aggressiveness of Prostate Cancer Cells Is Linked with Deregulated Expression of VEGF, IL-6 and miRNAs That Are Attenuated by CDF [J].
Bao, Bin ;
Ahmad, Aamir ;
Kong, Dejuan ;
Ali, Shadan ;
Azmi, Asfar S. ;
Li, Yiwei ;
Banerjee, Sanjeev ;
Padhye, Subhash ;
Sarkar, Fazlul H. .
PLOS ONE, 2012, 7 (08)