Cookies help us deliver our services. By using our services, you agree to our use of cookies. More information

Padinharayil 2023 Cancers (Basel)

From Bioblast
Revision as of 16:33, 9 November 2023 by Tindle Lisa (talk | contribs)
(diff) ← Older revision | Latest revision (diff) | Newer revision β†’ (diff)
Publications in the MiPMap
Padinharayil H, Rai V, George A (2023) Mitochondrial metabolism in pancreatic ductal adenocarcinoma: from mechanism-based perspectives to therapy. https://doi.org/10.3390/cancers15041070

Β» Cancers (Basel) 15:1070. PMID: 36831413 Open Access

Padinharayil Hafiza, Rai Vikrant, George Alex (2023) Cancers (Basel)

Abstract: Pancreatic ductal adenocarcinoma (PDAC), the fourteenth most common malignancy, is a major contributor to cancer-related death with the utmost case fatality rate among all malignancies. Functional mitochondria, regardless of their complex ecosystem relative to normal cells, are essential in PDAC progression. Tumor cells' potential to produce ATP as energy, despite retaining the redox potential optimum, and allocating materials for biosynthetic activities that are crucial for cell growth, survival, and proliferation, are assisted by mitochondria. The polyclonal tumor cells with different metabolic profiles may add to carcinogenesis through inter-metabolic coupling. Cancer cells frequently possess alterations in the mitochondrial genome, although they do not hinder metabolism; alternatively, they change bioenergetics. This can further impart retrograde signaling, educate cell signaling, epigenetic modifications, chromatin structures, and transcription machinery, and ultimately satisfy cancer cellular and nuclear demands. To maximize the tumor microenvironment (TME), tumor cells remodel nearby stromal cells and extracellular matrix. These changes initiate polyclonality, which is crucial for growth, stress response, and metastasis. Here, we evaluate all the intrinsic and extrinsic pathways drawn by mitochondria in carcinogenesis, emphasizing the perspectives of mitochondrial metabolism in PDAC progression and treatment. β€’ Keywords: Extracellular matrix, Immune cells, Metabolism, Mitochondria, Pancreatic ductal adenocarcinoma, Retrograde signaling, Therapy β€’ Bioblast editor: Plangger M


Labels: Pathology: Cancer