Increased expression of leucine‐rich α‐2 glycoprotein 1 as a predictive biomarker of favorable progression‐free survival in meningioma

Author:

Moritsubo Mayuko1ORCID,Furuta Takuya1ORCID,Miyoshi Junko12,Komaki Satoru12,Sakata Kiyohiko2ORCID,Miyoshi Hiroaki1ORCID,Morioka Motohiro2ORCID,Ohshima Koichi1ORCID,Sugita Yasuo13ORCID

Affiliation:

1. Department of Pathology Kurume University School of Medicine Kurume Japan

2. Department of Neurosurgery Kurume University School of Medicine Kurume Japan

3. Department of Neuropathology St. Mary's Hospital Kurume Japan

Abstract

Most meningiomas, which are frequent central nervous system tumors, are classified as World Health Organization (WHO) grade 1 because of their slow‐growing nature. However, the recurrence rate varies and is difficult to predict using conventional histopathological diagnoses. Leucine‐rich α‐2 glycoprotein 1 (LRG1) is involved in cell signal transduction, cell adhesion, and DNA repair and is a predictive biomarker in different malignant tumors; however, such a relationship has not been reported in meningiomas. We examined tissue microarrays of histological samples from 117 patients with grade 1 and 2 meningiomas and assessed their clinical and pathological features, including expression of LRG1 protein. LRG1‐high meningiomas showed an increased number of vessels with CD3‐positive cell infiltration (P = 0.0328) as well as higher CD105‐positive vessels (P = 0.0084), as compared to LRG1‐low cases. They also demonstrated better progression‐free survival (hazard ratio [HR] 0.11, 95% confidence interval [CI] 0.016–0.841) compared to LRG1‐low patients (P = 0.033). Moreover, multivariate analysis indicated that high LRG1 expression was an independent prognostic factor (HR, 0.13; 95% CI, 0.018–0.991; P = 0.049). LRG1 immunohistochemistry may be a convenient tool for estimating the prognosis of meningiomas in routine practice. Further studies are required to elucidate the key role of LRG1 in meningioma progression.

Funder

Fukuoka Public Health Promotion Organization Cancer Research Fund

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

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