Pancreatic cancer is the cancer-type inducing the most severe cachectic phenotype. Recent studies describe ZIP4 as a main factor inducing pancreatic cancer through oncogenic miR-373 up regulation. The purpose of this study is to identify circular RNAs (circRNAs) able to mitigate the oncogenic activity of the ZIP4/miR-373 pathway. This study reveales circANAPC7 as a novel tumor suppressor, capable of buffering miR-373 molecules with a consequent increase of PHPLPP2 phosphatase activity. Accordingly, AKT/STAT5 pathway is downregulated such as the release of muscle wasting molecule TGF- β. In my thesis, I am describing this recent scientific manuscript, recently published, deeply discussing the scientific questions driving this work and the techniques applied to solve them.
Pancreatic cancer is the cancer-type inducing the most severe cachectic phenotype. Recent studies describe ZIP4 as a main factor inducing pancreatic cancer through oncogenic miR-373 up regulation. The purpose of this study is to identify circular RNAs (circRNAs) able to mitigate the oncogenic activity of the ZIP4/miR-373 pathway. This study reveales circANAPC7 as a novel tumor suppressor, capable of buffering miR-373 molecules with a consequent increase of PHPLPP2 phosphatase activity. Accordingly, AKT/STAT5 pathway is downregulated such as the release of muscle wasting molecule TGF- β. In my thesis, I am describing this recent scientific manuscript, recently published, deeply discussing the scientific questions driving this work and the techniques applied to solve them.
Circular RNA ANAPC7 Inhibits Tumor Growth and Muscle Wasting via PHLPP2–AKT–TGF-b Signaling Axis in Pancreatic Cancer.
GRAZIANO, SAMUELE
2022/2023
Abstract
Pancreatic cancer is the cancer-type inducing the most severe cachectic phenotype. Recent studies describe ZIP4 as a main factor inducing pancreatic cancer through oncogenic miR-373 up regulation. The purpose of this study is to identify circular RNAs (circRNAs) able to mitigate the oncogenic activity of the ZIP4/miR-373 pathway. This study reveales circANAPC7 as a novel tumor suppressor, capable of buffering miR-373 molecules with a consequent increase of PHPLPP2 phosphatase activity. Accordingly, AKT/STAT5 pathway is downregulated such as the release of muscle wasting molecule TGF- β. In my thesis, I am describing this recent scientific manuscript, recently published, deeply discussing the scientific questions driving this work and the techniques applied to solve them.File | Dimensione | Formato | |
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https://hdl.handle.net/20.500.12608/48961