Transcriptomic profiling of intermediate cell carcinoma of the liver

Author:

Jang Byungchan12ORCID,Kwon So Mee1ORCID,Kim Jang Hyun12,Kim Jung Mo3ORCID,Chung Taek4ORCID,Yoo Jeong Eun45ORCID,Kim Haeryoung6ORCID,Calderaro Julien7ORCID,Woo Hyun Goo123ORCID,Park Young Nyun45ORCID

Affiliation:

1. Department of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea

2. Department of Biomedical Science, Graduate School, Ajou University, Suwon, Republic of Korea

3. Ajou Translational Omics Center (ATOC), Research Institute for Innovative Medicine, Ajou University Medical Center, Suwon, Republic of Korea

4. Department of Pathology, Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University College of Medicine, Seoul, Republic of Korea

5. Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Republic of Korea

6. Department of Pathology, Seoul National University College of Medicine, Seoul, Republic of Korea

7. Department of Pathology, Assistance Publique Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Créteil, France

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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