| Literature DB >> 32443847 |
Toshio Fujisawa1,2,3, Takeshi Shimamura4, Kaku Goto2, Ryo Nakagawa2, Ryosuke Muroyama2, Yoshinori Ino5, Hajime Horiuchi6, Itaru Endo7, Shin Maeda8, Yasushi Harihara9, Atsushi Nakajima4, Nobuyuki Matsuhashi10, Naoya Kato2, Hiroyuki Isayama1, Ankit Puri3, Akiko Suzuki3, Ian Bellayr3, Pamela Leland3, Bharat H Joshi3, Raj K Puri3.
Abstract
Perineural invasion (PNI) is one of the major pathological characteristics of pancreatic ductal adeno-carcinoma (PDAC), which is mediated by invading cancer cells into nerve cells. Herein, we identify the overexpression of Interleukin-13 Receptor alpha2 (IL-13Rα2) in the PNI from 236 PDAC samples by studying its expression at the protein levels by immunohistochemistry (IHC) and the RNA level by in situ hybridization (ISH). We observe that ≥75% samples overexpressed IL-13Rα2 by IHC and ISH in grade 2 and 3 tumors, while ≥64% stage II and III tumors overexpressed IL-13Rα2 (≥2+). Interestingly, ≥36 % peripancreatic neural plexus (PL) and ≥70% nerve endings (Ne) among PNI in PDAC samples showed higher levels of IL-13Rα2 (≥2+). IL-13Rα2 +ve PL and Ne subjects survived significantly less than IL-13Rα2 -ve subjects, suggesting that IL-13Rα2 may have a unique role as a biomarker of PNI-aggressiveness. Importantly, IL-13Rα2 may be a therapeutic target for intervention, which might not only prolong patient survival but also help alleviate pain attributed to perineural invasion. Our study uncovers a novel role of IL-13Rα2 in PNI as a key factor of the disease severity, thus revealing a therapeutically targetable option for PDAC and to facilitate PNI-associated pain management.Entities:
Keywords: IL-13Rα2; pancreatic ductal adenocarcinoma; perineural invasion; prognosis
Year: 2020 PMID: 32443847 DOI: 10.3390/cancers12051294
Source DB: PubMed Journal: Cancers (Basel) ISSN: 2072-6694 Impact factor: 6.639