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Coexisting mechanisms of luminogenesis in pancreatic cancer-derived organoids. | LitMetric

Coexisting mechanisms of luminogenesis in pancreatic cancer-derived organoids.

iScience

Technical University of Munich, TUM School of Natural Sciences, Department of Bioscience, Chair for Cellular Biophysics E27, 85748 Garching, Germany.

Published: July 2024

AI Article Synopsis

  • Lumens play a vital role in the architecture of both healthy pancreas tissues and precancerous pancreatic ductal adenocarcinoma (PDAC) lesions, facilitating enzyme transport and cyst-like structures.
  • Pancreatic-cancer organoids replicate critical features of both healthy and diseased pancreas, but the transition to hollowness in these structures is not well understood.
  • The study identifies two key mechanisms for lumen formation in these organoids: one involves fluid intake leading to multiple microlumen merging, and the other is through the death of central cells, creating hollow spaces.

Article Abstract

Lumens are crucial features of the tissue architecture in both the healthy exocrine pancreas, where ducts shuttle enzymes from the acini to the intestine, and in the precancerous lesions of the highly lethal pancreatic ductal adenocarcinoma (PDAC), similarly displaying lumens that can further develop into cyst-like structures. Branched pancreatic-cancer derived organoids capture key architectural features of both the healthy and diseased pancreas, including lumens. However, their transition from a solid mass of cells to a hollow tissue remains insufficiently explored. Here, we show that organoids display two orthogonal but complementary lumen formation mechanisms: one relying on fluid intake for multiple microlumen nucleation, swelling and fusion, and the other involving the death of a central cell population, thereby hollowing out cavities. These results shed further light on the processes of luminogenesis, deepening our understanding of the early formation of PDAC precancerous lesions, including cystic neoplasia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11269295PMC
http://dx.doi.org/10.1016/j.isci.2024.110299DOI Listing

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