J Pathol Transl Med.  2016 Jul;50(4):264-269. 10.4132/jptm.2016.04.24.

Significance of Parafibromin Expression in Laryngeal Squamous Cell Carcinomas

Affiliations
  • 1Department of Pathology, Chosun University School of Medicine, Gwangju, Korea. nanih@chosun.ac.kr

Abstract

BACKGROUND
Parafibromin is a product of the tumor suppressor gene that has been studied as a potential indicator of tumor aggressiveness in the parathyroid, breast, colorectum, and stomach. However, the clinical significance and potential function of parafibromin expression in head and neck squamous cell carcinomas remain largely unknown. The aim of this study was to evaluate the expression of parafibromin in laryngeal squamous cell carcinoma (LSCC) and to verify its potential as a biomarker of tumor behavior.
METHODS
Parafibromin expression was evaluated in 30 cases of LSCC using immunohistochemistry. The correlations between parafibromin expression and clinicopathologic parameters were investigated.
RESULTS
Parafibromin expression was positive in 15 cases (50%) and negative in 15 cases (50%). Tumor size and T stage showed a statistically significant inverse relationship with parafibromin expression (p=.028 and p<.001, respectively). Parafibromin expression was not associated with age, sex, lymph node metastasis, tumor differentiation, or tumor location. There was no statistically significant relationship between parafibromin expression and progression-free survival in the patients (p>.05).
CONCLUSIONS
Our results indicate that the downregulation or loss of parafibromin expression can be employed as a novel marker of tumor progression or aggressiveness in LSCC.

Keyword

Parafibromin; Carcinoma, squamous cell; Epithelial-mesenchymal transition

MeSH Terms

Breast
Carcinoma, Squamous Cell*
Disease-Free Survival
Down-Regulation
Epithelial Cells*
Epithelial-Mesenchymal Transition
Genes, Tumor Suppressor
Head
Humans
Immunohistochemistry
Lymph Nodes
Neck
Neoplasm Metastasis
Stomach

Figure

  • Fig. 1. Parafibromin expression in squamous cell carcinoma of the larynx. (A) Parafibromin expressed in the basal layer of normal laryngeal mucosa. (B) Parafibromin-positive staining is expressed in the nuclei of tumor cells. (C) Occasionally, parafibromin positivity is observed in the periphery of the tumor nest. (D) Representative image of parafibromin-negative staining.

  • Fig. 2. Kaplan-Meier curves of progression-free survival in laryngeal squamous cell carcinoma patients according to parafibromin expression status. There is no statistically significant relationship between parafibromin expression and the progression-free survival of the patients (p>.05).


Reference

1. Genden EM, Ferlito A, Silver CE, et al. Evolution of the management of laryngeal cancer. Oral Oncol. 2007; 43:431–9.
Article
2. Li L, Wang J, Gao L, Gong L. Expression of paxillin in laryngeal squamous cell carcinoma and its prognostic value. Int J Clin Exp Pathol. 2015; 8:9232–9.
3. Marioni G, Marchese-Ragona R, Cartei G, Marchese F, Staffieri A. Current opinion in diagnosis and treatment of laryngeal carcinoma. Cancer Treat Rev. 2006; 32:504–15.
Article
4. Karaarslan S, Yaman B, Ozturk H, Kumbaraci BS. Parafibromin staining characteristics in urothelial carcinomas and relationship with prognostic parameters. J Pathol Transl Med. 2015; 49:389–95.
Article
5. Zhang Z, Yang XF, Huang KQ, et al. The clinicopathological significances and biological functions of parafibromin expression in head and neck squamous cell carcinomas. Tumour Biol. 2015; 36:9487–97.
Article
6. Newey PJ, Bowl MR, Thakker RV. Parafibromin: functional insights. J Intern Med. 2009; 266:84–98.
7. Carpten JD, Robbins CM, Villablanca A, et al. HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome. Nat Genet. 2002; 32:676–80.
8. Wang PF, Tan MH, Zhang C, Morreau H, Teh BT. HRPT2, a tumor suppressor gene for hyperparathyroidism-jaw tumor syndrome. Horm Metab Res. 2005; 37:380–3.
9. Yart A, Gstaiger M, Wirbelauer C, et al. The HRPT2 tumor suppressor gene product parafibromin associates with human PAF1 and RNA polymerase II. Mol Cell Biol. 2005; 25:5052–60.
10. Zhang C, Kong D, Tan MH, et al. Parafibromin inhibits cancer cell growth and causes G1 phase arrest. Biochem Biophys Res Commun. 2006; 350:17–24.
Article
11. Porzionato A, Macchi V, Barzon L, et al. Immunohistochemical assessment of parafibromin in mouse and human tissues. J Anat. 2006; 209:817–27.
Article
12. Gill AJ, Clarkson A, Gimm O, et al. Loss of nuclear expression of parafibromin distinguishes parathyroid carcinomas and hyperparathyroidism-jaw tumor (HPT-JT) syndrome-related adenomas from sporadic parathyroid adenomas and hyperplasias. Am J Surg Pathol. 2006; 30:1140–9.
Article
13. Selvarajan S, Sii LH, Lee A, et al. Parafibromin expression in breast cancer: a novel marker for prognostication? J Clin Pathol. 2008; 61:64–7.
Article
14. Zheng HC, Wei ZL, Xu XY, et al. Parafibromin expression is an independent prognostic factor for colorectal carcinomas. Hum Pathol. 2011; 42:1089–102.
Article
15. Zheng HC, Takahashi H, Li XH, et al. Downregulated parafibromin expression is a promising marker for pathogenesis, invasion, metastasis and prognosis of gastric carcinomas. Virchows Arch. 2008; 452:147–55.
Article
16. Howell VM, Haven CJ, Kahnoski K, et al. HRPT2 mutations are associated with malignancy in sporadic parathyroid tumours. J Med Genet. 2003; 40:657–63.
17. Licitra L, Bernier J, Grandi C, et al. Cancer of the larynx. Crit Rev Oncol Hematol. 2003; 47:65–80.
Article
Full Text Links
  • JPTM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr