Original Article

Split Viewer

Korean J Hematol 2012; 47(4):

Published online December 31, 2012

https://doi.org/10.5045/kjh.2012.47.4.267

© The Korean Society of Hematology

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis

Jong-Jin Seo1, Taeshik Cho2, Sun-Young Kim3*, Ibrahim Nassour3, Hee-Jin Kim4, Yeon-Jung Lim5, Kyung-Nam Koh1, and Ho-Joon Im1

1Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Ulsan College of Medicine & Asan Medical Center, Seoul, Korea.

2Department of Pediatrics, Hanyang University Medical Center, Seoul, Korea.

3Department of Surgery, Pittsburgh University, Pittsburgh, PA, USA.

4Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

5Department of Pediatrics, Chungnam National University College of Medicine, Daejeon, Korea.

Correspondence to : Correspondence to Sun-Young Kim, M.D., Ph.D. Department of Surgery, Pittsburgh University, NW641 MUH, 3459 Fifth Avenue, Pittsburgh, PA 15213, USA. Tel: +1-412-721-3319, Fax: +1-412-647-5959, nel1205@hanmail.net, kimsy@upmc.edu

Received: May 9, 2012; Revised: August 23, 2012; Accepted: November 6, 2012

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Gelsolin and matrix metalloproteinase 12 (MMP12) expression has been reported in Langerhans cell histiocytosis (LCH), but the clinical significance of this expression is unknown. We investigated the associations of these proteins with clinical manifestations in patients diagnosed with LCH.

Methods

We performed a retrospective analysis of clinical data from patients diagnosed with LCH and followed up between 1998 and 2008. Available formalin-fixed, paraffin-embedded specimens were used for gelsolin and MMP12 immunohistochemical staining. We analyzed the expression levels of these proteins and their associations with LCH clinical features.

Results

Specimens from 36 patients (20 males, 16 females) with a diagnosis of LCH based on CD1a positivity with clinical manifestations were available for immunohistochemical staining. Median patient age was 62 months (range, 5 to 207). The expression of gelsolin varied; it was high in 17 patients (47.2%), low in 11 patients (30.6%), and absent in 8 patients (22.2%). The high gelsolin expression group had a higher tendency for multi-organ and risk organ involvement, although the trend was not statistically significant. MMP12 was detected only in 7 patients (19.4%) who showed multi-system involvement (P=0.018) and lower event-free survival (P=0.002) in comparison to patients with negative MMP12 staining.

Conclusion

Gelsolin and MMP12 expression may be associated with the clinical course of LCH, and MMP12 expression may be particularly associated with severe LCH. Further studies of larger populations are needed to define the precise role and significance of gelsolin and MMP12 in the pathogenesis of LCH.

Keywords Histiocytosis, Langerhans cells, Immunohistochemistry, Gelsolin, Matrix Metalloproteinase 12

Article

Original Article

Korean J Hematol 2012; 47(4): 267-272

Published online December 31, 2012 https://doi.org/10.5045/kjh.2012.47.4.267

Copyright © The Korean Society of Hematology.

Prognostic significance of gelsolin and MMP12 in Langerhans cell histiocytosis

Jong-Jin Seo1, Taeshik Cho2, Sun-Young Kim3*, Ibrahim Nassour3, Hee-Jin Kim4, Yeon-Jung Lim5, Kyung-Nam Koh1, and Ho-Joon Im1

1Division of Pediatric Hematology/Oncology, Department of Pediatrics, University of Ulsan College of Medicine & Asan Medical Center, Seoul, Korea.

2Department of Pediatrics, Hanyang University Medical Center, Seoul, Korea.

3Department of Surgery, Pittsburgh University, Pittsburgh, PA, USA.

4Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

5Department of Pediatrics, Chungnam National University College of Medicine, Daejeon, Korea.

Correspondence to: Correspondence to Sun-Young Kim, M.D., Ph.D. Department of Surgery, Pittsburgh University, NW641 MUH, 3459 Fifth Avenue, Pittsburgh, PA 15213, USA. Tel: +1-412-721-3319, Fax: +1-412-647-5959, nel1205@hanmail.net, kimsy@upmc.edu

Received: May 9, 2012; Revised: August 23, 2012; Accepted: November 6, 2012

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Gelsolin and matrix metalloproteinase 12 (MMP12) expression has been reported in Langerhans cell histiocytosis (LCH), but the clinical significance of this expression is unknown. We investigated the associations of these proteins with clinical manifestations in patients diagnosed with LCH.

Methods

We performed a retrospective analysis of clinical data from patients diagnosed with LCH and followed up between 1998 and 2008. Available formalin-fixed, paraffin-embedded specimens were used for gelsolin and MMP12 immunohistochemical staining. We analyzed the expression levels of these proteins and their associations with LCH clinical features.

Results

Specimens from 36 patients (20 males, 16 females) with a diagnosis of LCH based on CD1a positivity with clinical manifestations were available for immunohistochemical staining. Median patient age was 62 months (range, 5 to 207). The expression of gelsolin varied; it was high in 17 patients (47.2%), low in 11 patients (30.6%), and absent in 8 patients (22.2%). The high gelsolin expression group had a higher tendency for multi-organ and risk organ involvement, although the trend was not statistically significant. MMP12 was detected only in 7 patients (19.4%) who showed multi-system involvement (P=0.018) and lower event-free survival (P=0.002) in comparison to patients with negative MMP12 staining.

Conclusion

Gelsolin and MMP12 expression may be associated with the clinical course of LCH, and MMP12 expression may be particularly associated with severe LCH. Further studies of larger populations are needed to define the precise role and significance of gelsolin and MMP12 in the pathogenesis of LCH.

Keywords: Histiocytosis, Langerhans cells, Immunohistochemistry, Gelsolin, Matrix Metalloproteinase 12

Fig 1.

Figure 1.

Light micrographs of LCH lesions after gelsolin immunohistochemical staining (×400). Scattered LCs with reddish brown reactions in the cytoplasm were considered positive. A semi-quantitative evaluation was made using the following grading system: negative (A), lower expression group (LEG) (B) and higher expression group (HEG) (C) according to the extent of cytoplasmic staining.

Blood Research 2012; 47: 267-272https://doi.org/10.5045/kjh.2012.47.4.267

Fig 2.

Figure 2.

Light micrographs of LCH lesions after MMP12 immunohistochemical staining (400×). Slides with no staining were regarded as negative (A), whereas LCs with light brown reactions in the cytoplasm were considered positive (B).

Blood Research 2012; 47: 267-272https://doi.org/10.5045/kjh.2012.47.4.267

Fig 3.

Figure 3.

Event-free survival (EFS) rates according to immunohistochemical grade. (A) The probability of EFS according to the gelsolin expression. The EFS was 94.7% for LEG patients and 78.6% for HEG patients. The difference was not statistically significant according to the log-rank test (P=0.222). (B) The probability of EFS in terms of MMP positivity. EFS for the negative group was 96.6%, while that of the positive group was 57.1%, a statistically significant difference according to the log-rank test (P=0.002).

Blood Research 2012; 47: 267-272https://doi.org/10.5045/kjh.2012.47.4.267

Table 1 . Clinical manifestations according to the immunohistochemistry..


Table 2 . Organ involvement according to immunohistochemistry..


Blood Res
Volume 59 2024

Stats or Metrics

Share this article on

  • line

Related articles in BR

Blood Research

pISSN 2287-979X
eISSN 2288-0011
qr-code Download