The expression and significance of multi-drug resistance genes in breast cancer stem cells

2008 ◽  
Vol 7 (9) ◽  
pp. 538-541 ◽  
Author(s):  
Zhi Li ◽  
Chunping Liu ◽  
Yanli He ◽  
Jinghui Zhang ◽  
Tao Huang
2021 ◽  
Vol 11 ◽  
Author(s):  
Qinghui Zheng ◽  
Mengdi Zhang ◽  
Fangfang Zhou ◽  
Long Zhang ◽  
Xuli Meng

Drug resistance is a major challenge in breast cancer (BC) treatment at present. Accumulating studies indicate that breast cancer stem cells (BCSCs) are responsible for the BC drugs resistance, causing relapse and metastasis in BC patients. Thus, BCSCs elimination could reverse drug resistance and improve drug efficacy to benefit BC patients. Consequently, mastering the knowledge on the proliferation, resistance mechanisms, and separation of BCSCs in BC therapy is extremely helpful for BCSCs-targeted therapeutic strategies. Herein, we summarize the principal BCSCs surface markers and signaling pathways, and list the BCSCs-related drug resistance mechanisms in chemotherapy (CT), endocrine therapy (ET), and targeted therapy (TT), and display therapeutic strategies for targeting BCSCs to reverse drug resistance in BC. Even more importantly, more attention should be paid to studies on BCSC-targeted strategies to overcome the drug resistant dilemma of clinical therapies in the future.


2018 ◽  
Vol 24 (4) ◽  
pp. 701-703 ◽  
Author(s):  
Mohamed Kamal ◽  
Ebtesam H.O. Nafie ◽  
Shimaa Elsers ◽  
Salma Alanwar ◽  
Rawayeh Ibrahim ◽  
...  

2016 ◽  
Vol 8 (6) ◽  
pp. 704-711 ◽  
Author(s):  
Parthasarathy Arumugam ◽  
Joon Myong Song

Total internal reflection fluorescence microscopy (TIRF) and Qdot probe based analytical method for the simultaneous evaluation of the cytotoxic ability of camptothecin and the drug resistance profile upon the inhibition of drug efflux pumps in breast cancer stem cells.


2021 ◽  
Vol 22 (9) ◽  
pp. 4673
Author(s):  
Vrinda Gote ◽  
Anantha Ram Nookala ◽  
Pradeep Kumar Bolla ◽  
Dhananjay Pal

Breast cancer, specifically metastatic breast, is a leading cause of morbidity and mortality in women. This is mainly due to relapse and reoccurrence of tumor. The primary reason for cancer relapse is the development of multidrug resistance (MDR) hampering the treatment and prognosis. MDR can occur due to a multitude of molecular events, including increased expression of efflux transporters such as P-gp, BCRP, or MRP1; epithelial to mesenchymal transition; and resistance development in breast cancer stem cells. Excessive dose dumping in chemotherapy can cause intrinsic anti-cancer MDR to appear prior to chemotherapy and after the treatment. Hence, novel targeted nanomedicines encapsulating chemotherapeutics and gene therapy products may assist to overcome cancer drug resistance. Targeted nanomedicines offer innovative strategies to overcome the limitations of conventional chemotherapy while permitting enhanced selectivity to cancer cells. Targeted nanotheranostics permit targeted drug release, precise breast cancer diagnosis, and importantly, the ability to overcome MDR. The article discusses various nanomedicines designed to selectively target breast cancer, triple negative breast cancer, and breast cancer stem cells. In addition, the review discusses recent approaches, including combination nanoparticles (NPs), theranostic NPs, and stimuli sensitive or “smart” NPs. Recent innovations in microRNA NPs and personalized medicine NPs are also discussed. Future perspective research for complex targeted and multi-stage responsive nanomedicines for metastatic breast cancer is discussed.


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