Identification of a combined biomarker for malignant transformation in oral submucous fibrosis

被引:31
作者
Bazarsad, Shadavlonjid [1 ,2 ]
Zhang, Xianglan [1 ,3 ]
Kim, Ki-Yeol [1 ,4 ]
Illeperuma, Rasika [5 ]
Jayasinghe, Ruwan D. [6 ]
Tilakaratne, Wanninayake M. [7 ]
Kim, Jin [1 ]
机构
[1] Yonsei Univ, Coll Dent, Oral Canc Res Inst, Dept Oral Pathol, Seoul 120752, South Korea
[2] Mongolian Natl Univ Med Sci, Dent Sch, Ulaanbaatar, Mongolia
[3] Yanbian Univ Hosp, Dept Pathol, Yanji, Peoples R China
[4] Yonsei Univ, Coll Dent, Brain Korea Plus Project 21, Seoul, South Korea
[5] Univ Peradeniya, Fac Allied Hlth Sci, Dept Med Lab Sci, Peradeniya, Sri Lanka
[6] Univ Peradeniya, Fac Dent Sci, Dept Oral Med & Periodontol, Peradeniya, Sri Lanka
[7] Univ Peradeniya, Fac Dent Sci, Dept Oral Pathol, Peradeniya, Sri Lanka
关键词
combined biomarkers; oral submucous fibrosis; risk assessment; squamous cell carcinoma; SQUAMOUS-CELL CARCINOMA; BETA-CATENIN; EXPRESSION; CANCER; PROGRESSION; PROTEIN; HEAD; MET; METASTASIS; FREQUENCY;
D O I
10.1111/jop.12483
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
BACKGROUND: Oral submucous fibrosis (OSF) is a chronic progressive disease of the oral cavity that is considered a common potentially malignant disorder in South Asia. Areca nut chewing is the main etiological factor, but its carcinogenic mechanism has yet to be proven. The purpose of this study was to identify the useful biomarkers in predicting high-risk patients with OSF. METHODS: Thirty-six cases of OSF and six cases of normal oral mucosa (NOM) were used for this study. Immunohistochemical staining was performed for Ki67, cyclin D1, p16, p53, beta-catenin, c-Jun, c-Met, and insulin-like growth factor II mRNA-binding protein 3 (IMP3). The expression patterns of NOM served as guidelines for the scoring system. RESULTS: The expression of Ki67, cyclin D1, c-Met, IMP3, and beta-catenin showed a significant difference between OSF and NOM samples. The combined biomarkers of Ki67 and p16 showed significantly different expression between the transformation and non-transformation groups. With discriminant analysis, we proposed a noble formula and cutoff value for predicting high-risk patients with OSF. CONCLUSION: The notable biomarkers in our present study were Ki67 and p16 showing significantly different expression levels between the transformation and non-transformation groups. With the identification of high-risk patients with OSF, we can expect to develop more intensive treatment modalities, leading to the reduction in cancer transformation rate from OSF.
引用
收藏
页码:431 / 438
页数:8
相关论文
共 30 条
[1]   Oral submucous fibrosis: A clinicopathologic review of 205 cases in Indians [J].
Angadi P.V. ;
Rekha K.P. .
Oral and Maxillofacial Surgery, 2011, 15 (1) :15-19
[2]   Oral submucous fibrosis: an overview of the aetiology, pathogenesis, classification, and principles of management [J].
Arakeri, Gururaj ;
Brennan, Peter A. .
BRITISH JOURNAL OF ORAL & MAXILLOFACIAL SURGERY, 2013, 51 (07) :587-593
[3]   Nuclear accumulation of beta-catenin is a common and early event during neoplastic progression of Barrett esophagus [J].
Bian, YS ;
Osterheld, MC ;
Bosman, FT ;
Fontolliet, C ;
Benhattar, J .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2000, 114 (04) :583-590
[4]   Nuclear and cytoplasmic expression of Met in oral squamous cell carcinoma and in an organotypic oral cancer model [J].
Brusevold, Ingvild J. ;
Soland, Tine M. ;
Khuu, Cuong ;
Christoffersen, Thoralf ;
Bryne, Magne .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2010, 118 (04) :342-349
[5]   FREQUENCY OF HOMOZYGOUS DELETION AT P16/CDKN2 IN PRIMARY HUMAN TUMORS [J].
CAIRNS, P ;
POLASCIK, TJ ;
EBY, Y ;
TOKINO, K ;
CALIFANO, J ;
MERLO, A ;
MAO, L ;
HERATH, J ;
JENKINS, R ;
WESTRA, W ;
RUTTER, JL ;
BUCKLER, A ;
GABRIELSON, E ;
TOCKMAN, M ;
CHO, KR ;
HEDRICK, L ;
BOVA, GS ;
ISAACS, W ;
KOCH, W ;
SCHWAB, D ;
SIDRANSKY, D .
NATURE GENETICS, 1995, 11 (02) :210-212
[6]   Areca nut-induced buccal mucosa fibroblast contraction and its signaling: a potential role in oral submucous fibrosis-a precancer condition [J].
Chang, Mei-Chi ;
Lin, Li-Deh ;
Wu, Hui-Lin ;
Ho, Yuan-Soon ;
Hsien, Hsiang-Chi ;
Wang, Tong-Mei ;
Jeng, Po-Yuan ;
Cheng, Ru-Hsiu ;
Hahn, Liang-Jiunn ;
Jeng, Jiiang-Huei .
CARCINOGENESIS, 2013, 34 (05) :1096-1104
[7]   Expression of hepatocyte growth factor and c-met protein is significantly associated with the progression of oral squamous cell carcinoma in Taiwan [J].
Chen, YS ;
Wang, JT ;
Chang, YF ;
Liu, BY ;
Wang, YP ;
Sun, A ;
Chiang, CP .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 2004, 33 (04) :209-217
[8]   p16 Protein Expression and Human Papillomavirus Status As Prognostic Biomarkers of Nonoropharyngeal Head and Neck Squamous Cell Carcinoma [J].
Chung, Christine H. ;
Zhang, Qiang ;
Kong, Christina S. ;
Harris, Jonathan ;
Fertig, Elana J. ;
Harari, Paul M. ;
Wang, Dian ;
Redmond, Kevin P. ;
Shenouda, George ;
Trotti, Andy ;
Raben, David ;
Gillison, Maura L. ;
Jordan, Richard C. ;
Quynh-Thu Le .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (35) :3930-U212
[9]   Suprabasal p53 immunoexpression is strongly associated with high grade dysplasia and risk for malignant transformation in potentially malignant oral lesions from Northern Ireland [J].
Cruz, I ;
Napier, SS ;
van der Waal, I ;
Snijders, PJF ;
Walboomers, JMM ;
Lamey, PJ ;
Cowan, CG ;
Gregg, TA ;
Maxwell, P ;
Meijer, CJLM .
JOURNAL OF CLINICAL PATHOLOGY, 2002, 55 (02) :98-104
[10]   Expression of cyclin D1 and Ki-67 in squamous cell carcinoma of the oral cavity:: clinicopathological and prognostic significance [J].
de Vicente, JC ;
Herrero-Zapatero, A ;
Fresno, MF ;
López-Arranz, JS .
ORAL ONCOLOGY, 2002, 38 (03) :301-308