High N6‐methyladenosine‐activated TCEAL8 mRNA is a novel pancreatic cancer marker

Author:

Hara Tomoaki1,Meng Sikun1,Sato Hiromichi12,Tatekawa Shotaro3,Sasaki Kazuki12,Takeda Yu12ORCID,Tsuji Yoshiko1,Arao Yasuko1,Ofusa Ken14,Kitagawa Toru125,Yamada Daisaku2ORCID,Takahashi Hidenori2ORCID,Kobayashi Shogo2,Motooka Daisuke6,Suzuki Yutaka7,Rennie Sarah8,Uchida Shizuka9,Mori Masaki10,Ogawa Kazuhiko3,Doki Yuichiro2,Eguchi Hidetoshi2ORCID,Ishii Hideshi1ORCID

Affiliation:

1. Department of Medical Data Science, Center of Medical Innovation and Translational Research Osaka University Graduate School of Medicine Suita Osaka Japan

2. Department of Gastroenterological Surgery Osaka University Graduate School of Medicine Suita Osaka Japan

3. Department of Radiation Oncology Osaka University Graduate School of Medicine Suita Osaka Japan

4. Prophoenix Division Food and Life‐Science Laboratory, IDEA Consultants, Inc. Osaka Osaka Japan

5. Kyowa‐kai Medical Corporation Kawanishi Hyogo Japan

6. Genome Information Research Center, Research Institute for Microbial Diseases Osaka University Suita Osaka Japan

7. Laboratory of Systems Genomics, Department of Computational Biology and Medical Sciences, Graduate School of Frontier Sciences The University of Tokyo Kashiwa‐shi Chiba Japan

8. Section for Computational and RNA Biology, Department of Biology University of Copenhagen Copenhagen Denmark

9. Department of Clinical Medicine, Center for RNA Medicine Aalborg University Copenhagen SV Denmark

10. Tokai University Graduate School of Medicine Isehara Kanagawa Japan

Abstract

AbstractN6‐methyladenosine (m6A) is an RNA modification involved in RNA processing and widely found in transcripts. In cancer cells, m6A is upregulated, contributing to their malignant transformation. In this study, we analyzed gene expression and m6A modification in cancer tissues, ducts, and acinar cells derived from pancreatic cancer patients using MeRIP‐seq. We found that dozens of RNAs highly modified by m6A were detected in cancer tissues compared with ducts and acinar cells. Among them, the m6A‐activated mRNA TCEAL8 was observed, for the first time, as a potential marker gene in pancreatic cancer. Spatially resolved transcriptomic analysis showed that TCEAL8 was highly expressed in specific cells, and activation of cancer‐related signaling pathways was observed relative to TCEAL8‐negative cells. Furthermore, among TCEAL8‐positive cells, the cells expressing the m6A‐modifying enzyme gene METTL3 showed co‐activation of Notch and mTOR signaling, also known to be involved in cancer metastasis. Overall, these results suggest that m6A‐activated TCEAL8 is a novel marker gene involved in the malignant transformation of pancreatic cancer.

Funder

Takahashi Industrial and Economic Research Foundation

Mitsubishi Foundation

Japan Science and Technology Agency

Publisher

Wiley

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