Erratum: Corrigendum: Rare cell variability and drug-induced reprogramming as a mode of cancer drug resistance

Nature ◽  
2018 ◽  
Vol 555 (7695) ◽  
pp. 274-274
Author(s):  
Sydney M. Shaffer ◽  
Margaret C. Dunagin ◽  
Stefan R. Torborg ◽  
Eduardo A. Torre ◽  
Benjamin Emert ◽  
...  
2019 ◽  
Vol 26 (2) ◽  
pp. 434-444 ◽  
Author(s):  
Hamdan S Al-malky ◽  
Sameer E Al Harthi ◽  
Abdel-Moneim M Osman

Background Doxorubicin is one of the most commonly prescribed and time-tested anticancer drugs. Although being considered as a first line drug in different types of cancers, the two main obstacles to doxorubicin therapy are drug-induced cardiotoxicity and drug resistance. Method The study utilizes systemic reviews on publications of previous studies obtained from scholarly journal databases including PubMed, Medline, Ebsco Host, Google Scholar, and Cochrane. The study utilizes secondary information obtained from health organizations using filters and keywords to sustain information relevancy. The study utilizes information retrieved from studies captured in the peer-reviewed journals on “doxorubicin-induced cardiotoxicity” and “doxorubicin resistance.” Discussion and results The exact mechanisms of cardiotoxicity are not known; various hypotheses are studied. Doxorubicin can lead to free radical generation in various ways. The commonly proposed underlying mechanisms promoting doxorubicin resistance are the expression of multidrug resistance proteins as well as other causes. Conclusion In this review, we have described the major obstacles to doxorubicin therapy, doxorubicin-induced cardiotoxicity as well as the mechanisms of cancer drug resistance and in following the treatment failures.


Nature ◽  
2017 ◽  
Vol 546 (7658) ◽  
pp. 431-435 ◽  
Author(s):  
Sydney M. Shaffer ◽  
Margaret C. Dunagin ◽  
Stefan R. Torborg ◽  
Eduardo A. Torre ◽  
Benjamin Emert ◽  
...  

2020 ◽  
Vol 20 (9) ◽  
pp. 779-787
Author(s):  
Kajal Ghosal ◽  
Christian Agatemor ◽  
Richard I. Han ◽  
Amy T. Ku ◽  
Sabu Thomas ◽  
...  

Chemotherapy employs anti-cancer drugs to stop the growth of cancerous cells, but one common obstacle to the success is the development of chemoresistance, which leads to failure of the previously effective anti-cancer drugs. Resistance arises from different mechanistic pathways, and in this critical review, we focus on the Fanconi Anemia (FA) pathway in chemoresistance. This pathway has yet to be intensively researched by mainstream cancer researchers. This review aims to inspire a new thrust toward the contribution of the FA pathway to drug resistance in cancer. We believe an indepth understanding of this pathway will open new frontiers to effectively treat drug-resistant cancer.


2019 ◽  
Vol 10 (26) ◽  
pp. 6693-6702 ◽  
Author(s):  
Wenyuan Zhao ◽  
Bin Shan ◽  
Dan He ◽  
Yuanda Cheng ◽  
Bin Li ◽  
...  

Author(s):  
Peng Xie ◽  
Yushu Wang ◽  
Dengshuai Wei ◽  
Lingpu Zhang ◽  
Bin Zhang ◽  
...  

The mechanisms of chemoresistance and nanoparticle-based drug delivery systems for platinum drugs were detailed summarized in this review. The current combination therapy provided an effective strategy to overcome the platinum drug resistance.


Author(s):  
Hai Wang ◽  
Pranay Agarwal ◽  
Gang Zhao ◽  
Guang Ji ◽  
Christopher M. Jewell ◽  
...  

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