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Survival-Associated Cellular Response Maintained in Pancreatic Ductal Adenocarcinoma (PDAC) Switched Between Soft and Stiff 3D Microgel Culture.
Atkins, Dixon J; Rosas, Jonah M; Månsson, Lisa K; Shahverdi, Nima; Dey, Siddharth S; Pitenis, Angela A.
Afiliação
  • Atkins DJ; Department of Biomolecular Science and Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Rosas JM; Department of Biomolecular Science and Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Månsson LK; Materials Department, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Shahverdi N; Molecular, Cellular, and Developmental Biology Department, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Dey SS; Department of Chemical Engineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
  • Pitenis AA; Department of Bioengineering, University of California Santa Barbara, Santa Barbara, California 93106, United States.
ACS Biomater Sci Eng ; 10(4): 2177-2187, 2024 04 08.
Article em En | MEDLINE | ID: mdl-38466617
ABSTRACT
Pancreatic ductal adenocarcinoma (PDAC) accounts for about 90% of all pancreatic cancer cases. Five-year survival rates have remained below 12% since the 1970s, in part due to the difficulty in detection prior to metastasis (migration and invasion into neighboring organs and glands). Mechanical memory is a concept that has emerged over the past decade that may provide a path toward understanding how invading PDAC cells "remember" the mechanical properties of their diseased ("stiff", elastic modulus, E ≈ 10 kPa) microenvironment even while invading a healthy ("soft", E ≈ 1 kPa) microenvironment. Here, we investigated the role of mechanical priming by culturing a dilute suspension of PDAC (FG) cells within a 3D, rheologically tunable microgel platform from hydrogels with tunable mechanical properties. We conducted a suite of acute (short-term) priming studies where we cultured PDAC cells in either a soft (E ≈ 1 kPa) or stiff (E ≈ 10 kPa) environment for 6 h, then removed and placed them into a new soft or stiff 3D environment for another 18 h. Following these steps, we conducted RNA-seq analyses to quantify gene expression. Initial priming in the 3D culture showed persistent gene expression for the duration of the study, regardless of the subsequent environments (stiff or soft). Stiff 3D culture was associated with the downregulation of tumor suppressors (LATS1, BCAR3, CDKN2C), as well as the upregulation of cancer-associated genes (RAC3). Immunofluorescence staining (BCAR3, RAC3) further supported the persistence of this cellular response, with BCAR3 upregulated in soft culture and RAC3 upregulated in stiff-primed culture. Stiff-primed genes were stratified against patient data found in The Cancer Genome Atlas (TCGA). Upregulated genes in stiff-primed 3D culture were associated with decreased survival in patient data, suggesting a link between patient survival and mechanical priming.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Microgéis Limite: Humans Idioma: En Revista: ACS Biomater Sci Eng / ACS biomater. sci. eng / ACS biomaterials science & engineering Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / Carcinoma Ductal Pancreático / Microgéis Limite: Humans Idioma: En Revista: ACS Biomater Sci Eng / ACS biomater. sci. eng / ACS biomaterials science & engineering Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos