Autophagy and multidrug resistance in cancer

Multidrug resistance (MDR) occurs frequently after long-term chemotherapy, resulting in refractory cancer and tumor recurrence. Therefore, combatting MDR is an important issue. Autophagy, a self-degradative system, universally arises during the treatment of sensitive and MDR cancer. Autophagy can be...

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Published inAi zheng Vol. 36; no. 8; pp. 342 - 351
Main Authors Li, Ying‐Jie, Lei, Yu‐He, Yao, Nan, Wang, Chen‐Ran, Hu, Nan, Ye, Wen‐Cai, Zhang, Dong‐Mei, Chen, Zhe‐Sheng
Format Journal Article
LanguageEnglish
Published London BioMed Central 24.06.2017
BioMed Central Ltd
John Wiley & Sons, Inc
Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, Guangdong, P.R.China%Institute of Traditional Chinese Medicine & Natural Products, College of Pharmacy, Jinan University, Guangzhou 510632, Guangdong, P.R.China
Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St.John's University, Queens, NY 11439, USA
BMC
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Summary:Multidrug resistance (MDR) occurs frequently after long-term chemotherapy, resulting in refractory cancer and tumor recurrence. Therefore, combatting MDR is an important issue. Autophagy, a self-degradative system, universally arises during the treatment of sensitive and MDR cancer. Autophagy can be a double-edged sword for MDR tumors: it participates in the development of MDR and protects cancer cells from chemotherapeutics but can also kill MDR cancer cells in which apoptosis pathways are inactive. Autophagy induced by anticancer drugs could also activate apoptosis signaling pathways in MDR cells, facilitating MDR reversal. Therefore, research on the regulation of autophagy to combat MDR is expanding and is becoming increasingly important. We summarize advanced studies of autophagy in MDR tumors, including the variable role of autophagy in MDR cancer cells.
Bibliography:44-1195/R
Ying‐Jie Li and Yu‐He Lei contributed equally to this work
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ISSN:1000-467X
2523-3548
1944-446X
1944-446X
2523-3548
DOI:10.1186/s40880-017-0219-2