Investigating the influence of taurochenodeoxycholic acid (TCDCA) on pancreatic cancer cell behavior An RNA Sequencing Approach /

Pancreatic cancer (PC) poses a substantial global health challenge, ranking as the fourth leading cause of cancer-related deaths due to its high mortality rate. Late-stage diagnoses are common due to the absence of specific symptoms. Pancreatic ductal adenocarcinoma (PDAC) accounts for the majority...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Gál Eleonóra
Parvaneh Shahram
Miklós Vanda
Hegyi Péter
Kemény Lajos
Veréb Zoltán
Venglovecz Viktória
Dokumentumtípus: Cikk
Megjelent: 2024
Sorozat:JOURNAL OF BIOTECHNOLOGY 391
Tárgyszavak:
doi:10.1016/j.jbiotec.2024.05.010

mtmt:34896328
Online Access:http://publicatio.bibl.u-szeged.hu/32469
Leíró adatok
Tartalmi kivonat:Pancreatic cancer (PC) poses a substantial global health challenge, ranking as the fourth leading cause of cancer-related deaths due to its high mortality rate. Late-stage diagnoses are common due to the absence of specific symptoms. Pancreatic ductal adenocarcinoma (PDAC) accounts for the majority of PC cases. Recent research has suggested a potential link between elevated serum levels of bile acids (BAs) and tumorigenesis of PDAC. This study aims to understand how taurochenodeoxycholic acid (TCDCA), a secondary BA, influences PDAC using RNA sequencing techniques on the Capan-1 cell line. We identified 2,950 differentially expressed genes (DEGs) following TCDCA treatment, with 1,597 upregulated and 1,353 downregulated genes. These DEGs were associated with critical PDAC pathways, including coagulation, angiogenesis, cell migration, and signaling regulation. Furthermore, we reviewed relevant literature highlighting genes like DKK-1, KRT80, UPLA, and SerpinB2, known for their roles in PDAC tumorigenesis and metastasis. Our study sheds light on the complex relationship between BAs and PDAC, offering insights into potential diagnostic markers and therapeutic targets. Further research is needed to unravel these findings' precise mechanisms and clinical implications, potentially improving PDAC diagnosis and treatment.
Terjedelem/Fizikai jellemzők:20-32
ISSN:0168-1656