Self-renewal signaling pathways in breast cancer stem cells

被引:30
作者
Nalla, Lakshmi Vineela [1 ]
Kalia, Kiran [1 ]
Khairnar, Amit [1 ]
机构
[1] NIPER, Dept Pharmacol & Toxicol, Gandhinagar, Gujarat, India
关键词
Self-renewal; Regulation; Cancer stem cell; Breast cancer; Sternness; EPITHELIAL-MESENCHYMAL TRANSITION; CROSS-TALK; LEPTIN RECEPTOR; IN-VITRO; ACTIVATION; NANOG; TUMORIGENESIS; INHIBITION; EXPRESSION; LEUKEMIA;
D O I
10.1016/j.biocel.2018.12.017
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
Breast cancer, a death-dealing disease mainly affects the women populace in the world. Outmoded remedial treatments like chemo and radiotherapy against breast cancer have manifold limitations like systemic and local toxicity resulting in the failure of treatment and cancer relapse. Recurrence and treatment failure is due to the presence of the minor number of cells in the tumor called cancer stem cells (CSCs) stocked with the properties like epithelial-mesenchymal transition, drug resistibility, auto self-renewability, and stemness. But, the sternness in these cells is different from the normal stem cells with regards to their self-renewal signaling pathways which gets dysregulated due to genomic and epigenome changes. In the earlier period's headway in the cancer research led to the advancement of new targets by understanding the pathophysiological mechanism behind cancer progression but still, the mortality rate i. the breast cancer is at its peak due to their unclear understanding of the sternness signaling regulations. The present review highlights the current clinical limitations in treating cancer stern cells and discusses the recent writings of their stemness signaling regulations required in maintenance of self-renewal capability and metastasis. More importantly, it further describes the present clinical and preclinical updates targeting cancer stem cells pathways. A strong consideration of these signalings and developing the treatment strategies with the existed chemotherapy may possibly offer a promising approach to eradicate cancer stern cells for improving the cancer survival rate to persuade a long-term clinical response.
引用
收藏
页码:140 / 153
页数:14
相关论文
共 153 条
[1]   Functional Antagonism between OTX2 and NANOG Specifies a Spectrum of Heterogeneous Identities in Embryonic Stem Cells [J].
Acampora, Dario ;
Di Giovannantonio, Luca Giovanni ;
Garofalo, Arcomaria ;
Nigro, Vincenzo ;
Omodei, Daniela ;
Lombardi, Alessia ;
Zhang, Jingchao ;
Chambers, Ian ;
Simeone, Antonio .
STEM CELL REPORTS, 2017, 9 (05) :1642-1659
[2]   Combination of drug-conjugated SWCNT nanocarriers for efficient therapy of cancer stem cells in a breast cancer animal model [J].
Al Faraj, Achraf ;
Shaik, Asma Sultana ;
Ratemi, Elaref ;
Halwani, Rabih .
JOURNAL OF CONTROLLED RELEASE, 2016, 225 :240-251
[3]   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
[4]  
[Anonymous], CANC GENE THER
[5]  
[Anonymous], BIORXIV
[6]  
[Anonymous], INT J CANC
[7]  
[Anonymous], PHYTOTHER RES
[8]  
[Anonymous], BIOMED RES
[9]  
[Anonymous], CANC RES
[10]  
[Anonymous], CANC RES CANRES