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Different Roles of Apoptosis and Autophagy in the Development of Human Colorectal Cancer

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MDPI
DOI: 10.3390/ijms241210201

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human colorectal cancer; apoptosis; autophagy; oxidative stress; non-coding-RNA; p53; NF-kB; SQSTM1; p62

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Colorectal cancer remains a major threat to life, despite attempts at therapeutic and screening. Apoptosis and autophagy share signaling pathways and protein components. In cancer development, these processes can interact and inhibit each other. Understanding the regulation and molecular mechanisms behind this duality is crucial.
Colorectal cancer (CRC) remains a major life-threatening malignancy, despite numerous therapeutic and screening attempts. Apoptosis and autophagy are two processes that share common signaling pathways, are linked by functional relationships and have similar protein components. During the development of cancer, the two processes can trigger simultaneously in the same cell, causing, in some cases, an inhibition of autophagy by apoptosis or apoptosis by autophagy. Malignant cells that have accumulated genetic alterations can take advantage of any alterations in the apoptotic process and as a result, progress easily in the cancerous transformation. Autophagy often plays a suppressive role during the initial stages of carcinogenicity, while in the later stages of cancer development it can play a promoting role. It is extremely important to determine the regulation of this duality of autophagy in the development of CRC and to identify the molecules involved, as well as the signals and the mechanisms behind it. All the reported experimental results indicate that, while the antagonistic effects of autophagy and apoptosis occur in an adverse environment characterized by deprivation of oxygen and nutrients, leading to the formation and development of CRC, the effects of promotion and collaboration usually involve an auxiliary role of autophagy compared to apoptosis. In this review, we elucidate the different roles of autophagy and apoptosis in human CRC development.

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