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Transcriptomic profiling of intermediate cell carcinoma of the liver

Authors
 Byungchan Jang  ;  So Mee Kwon  ;  Jang Hyun Kim  ;  Jung Mo Kim  ;  Taek Chung  ;  Jeong Eun Yoo  ;  Haeryoung Kim  ;  Julien Calderaro  ;  Hyun Goo Woo  ;  Young Nyun Park 
Citation
 HEPATOLOGY COMMUNICATIONS, Vol.8(8) : e0505, 2024-08 
Journal Title
HEPATOLOGY COMMUNICATIONS
Issue Date
2024-08
MeSH
Bile Duct Neoplasms / genetics ; Bile Duct Neoplasms / pathology ; Carcinoma, Hepatocellular* / genetics ; Carcinoma, Hepatocellular* / pathology ; Cholangiocarcinoma* / genetics ; Cholangiocarcinoma* / pathology ; Female ; Gene Expression Profiling* ; Gene Expression Regulation, Neoplastic ; Humans ; Liver Neoplasms* / genetics ; Liver Neoplasms* / pathology ; Male ; Methyltransferases / genetics ; Methyltransferases / metabolism ; Middle Aged ; Signal Transduction / genetics ; Transcriptome
Abstract
Background:Intermediate cell carcinoma (Int-CA) is a rare and enigmatic primary liver cancer characterized by uniform tumor cells exhibiting mixed features of both HCC and intrahepatic cholangiocarcinoma. Despite the unique pathological features of int-CA, its molecular characteristics remain unclear yet.Methods:RNA sequencing and whole genome sequencing profiling were performed on int-CA tumors and compared with those of HCC and intrahepatic cholangiocarcinoma.Results:Int-CAs unveiled a distinct and intermediate transcriptomic feature that is strikingly different from both HCC and intrahepatic cholangiocarcinoma. The marked abundance of splicing events leading to intron retention emerged as a signature feature of int-CA, along with a prominent expression of Notch signaling. Further exploration revealed that METTL16 was suppressed within int-CA, showing a DNA copy number-dependent transcriptional deregulation. Notably, experimental investigations confirmed that METTL16 suppression facilitated invasive tumor characteristics through the activation of the Notch signaling cascade.Conclusions:Our results provide a molecular landscape of int-CA featured by METTL16 suppression and frequent intron retention events, which may play pivotal roles in the acquisition of the aggressive phenotype of Int-CA.
Files in This Item:
T202404991.pdf Download
DOI
10.1097/HC9.0000000000000505
Appears in Collections:
1. College of Medicine (의과대학) > BioMedical Science Institute (의생명과학부) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pathology (병리학교실) > 1. Journal Papers
Yonsei Authors
Park, Young Nyun(박영년) ORCID logo https://orcid.org/0000-0003-0357-7967
Yoo, Jeong Eun(유정은) ORCID logo https://orcid.org/0000-0001-9990-279X
Chung, Taek(정택) ORCID logo https://orcid.org/0000-0001-7567-0680
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/200434
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