rBC2LCN-reactive SERPINA3 is a glycobiomarker candidate for pancreatic ductal adenocarcinoma

Author:

Mawaribuchi Shuuji1,Shimomura Osamu2,Oda Tatsuya2,Hiemori Keiko1,Shimizu Kayoko3,Yamase Kenya3,Date Mutsuhiro4,Tateno Hiroaki1ORCID

Affiliation:

1. Cellular and Molecular Biotechnology Research Institute, Multicellular System Regulation Research Group, National Institute of Advanced Industrial Science and Technology , Central 6, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8566 , Japan

2. Department of Surgery, University of Tsukuba , 1-1-1 Tennoudai, Tsukuba, Ibaraki 305-8575 , Japan

3. FUJIFILM Corporation , 6-1 Takada, Amagasaki, Hyogo 661-0963 , Japan

4. FUJIFILM Wako Pure Chemical Corporation , 3-8, Doshomachi 2-Chome, Chuo-ku, Osaka 540-8605 , Japan

Abstract

Abstract Early detection is urgently needed to improve the patient’s pancreatic ductal adenocarcinoma (PDAC) survival. Previously, we identified a novel tumor-associated glycan, H-type3, which is expressed on PDAC cells and is detected by rBC2LCN (recombinant N-terminal domain of BC2L-C identified from Burkholderia cenocepacia) lectin. Here, we identified that SERPINA3 is an rBC2LCN-reactive glycoprotein (BC2-S3) secreted from PDAC cells into the blood in patients with PDAC by liquid chromatography–tandem mass spectrometry analysis and lectin blotting. In immune staining, BC2-S3 was detected specifically in the tumor but not in normal tissues of PDAC. Lectin-ELISA was then developed to measure the serum level of BC2-S3 in healthy control (HC, n = 99) and patients with PDAC (n = 88). BC2-S3 exhibited higher in patients with PDAC than in those with HC. BC2-S3 showed similar diagnostic performance in all stages of PDAC (stages IA–IV, true positive rate = 76.1%, true negative rate = 81.8%) to CA19–9 (72.7%, 75.8%). Remarkably, BC2-S3 showed a significantly higher detection rate (89.7%) for early stage PDAC (IA–IIA) than CA19–9 (62.1%, P = 0.029). The combination of BC2-S3 and CA19–9 further improved the diagnostic ability for all stages of PDAC (81.8%, 87.9%). In conclusion, BC2-S3 is a glycobiomarker candidate for PDAC.

Funder

Translational Research Program

Innovative Medical Technology

AMED

Project for Cancer Research and Therapeutic Evolution

Kurata Grants, Hitachi Global Foundation for HT

Publisher

Oxford University Press (OUP)

Subject

Biochemistry

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