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Autophagy modulation in bladder cancer development and treatment

Identifieur interne : 000A22 ( Main/Exploration ); précédent : 000A21; suivant : 000A23

Autophagy modulation in bladder cancer development and treatment

Auteurs : Faping Li [République populaire de Chine] ; Hui Guo [République populaire de Chine] ; Yuxuan Yang [République populaire de Chine] ; Mingliang Feng [République populaire de Chine] ; Bin Liu [République populaire de Chine] ; Xiang Ren [République populaire de Chine] ; Honglan Zhou [République populaire de Chine]

Source :

RBID : PMC:6775810

Abstract

Bladder cancer (BC) is a potentially life-threatening malignancy. Due to a high recurrence rate, frequent surveillance strategies and intravesical drug therapies, BC is considered one of the most expensive tumors to treat. As a fundamental evolutionary catabolic process, autophagy plays an important role in the maintenance of cellular environmental homeostasis by degrading and recycling damaged cytoplasmic components, including macromolecules and organelles. Scientific studies in the last two decades have shown that autophagy acts as a double-edged sword with regard to the treatment of cancer. On one hand, autophagy inhibition is able to increase the sensitivity of cancer cells to treatment, a process known as protective autophagy. On the other hand, autophagy overactivation may lead to cell death, referred to as autophagic cell death, similar to apoptosis. Therefore, it is essential to identify the role of autophagy in cancer cells in order to develop novel therapeutic agents. In addition, autophagy may potentially become a novel therapeutic target in human diseases. In this review, the current knowledge on autophagy modulation in BC development and treatment is summarized.


Url:
DOI: 10.3892/or.2019.7286
PubMed: 31436298
PubMed Central: 6775810


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<p>Bladder cancer (BC) is a potentially life-threatening malignancy. Due to a high recurrence rate, frequent surveillance strategies and intravesical drug therapies, BC is considered one of the most expensive tumors to treat. As a fundamental evolutionary catabolic process, autophagy plays an important role in the maintenance of cellular environmental homeostasis by degrading and recycling damaged cytoplasmic components, including macromolecules and organelles. Scientific studies in the last two decades have shown that autophagy acts as a double-edged sword with regard to the treatment of cancer. On one hand, autophagy inhibition is able to increase the sensitivity of cancer cells to treatment, a process known as protective autophagy. On the other hand, autophagy overactivation may lead to cell death, referred to as autophagic cell death, similar to apoptosis. Therefore, it is essential to identify the role of autophagy in cancer cells in order to develop novel therapeutic agents. In addition, autophagy may potentially become a novel therapeutic target in human diseases. In this review, the current knowledge on autophagy modulation in BC development and treatment is summarized.</p>
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