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Evaluation of stromal myofibroblasts in oral submucous fibrosis and its malignant transformation: An immunohistochemical study.
Liu, Ziyi; Hu, Wenwu; Shan, Zhongyan; Liu, Sixuan; Yao, Zhigang; Quan, Hongzhi.
Afiliação
  • Liu Z; Department of Oral Maxillofacial Surgery, Central South University, Changsha, China.
  • Hu W; Department of Oral Maxillofacial Surgery, Yiyang Medical College, Yiyang, China.
  • Shan Z; Hunan Key Laboratory of Oral Health Research & Hunan 3D Printing Engineering Research Center of Oral Care & Hunan Clinical Research Center of Oral Major Diseases and Oral Health & Xiangya Stomatological Hospital and Xiangya School of Stomatology, Central South University, Changsha, China
  • Liu S; Department of Oral Maxillofacial Surgery, Central South University, Changsha, China.
  • Yao Z; Department of Oral Maxillofacial Surgery, Yiyang Medical College, Yiyang, China.
  • Quan H; Hunan Key Laboratory of Oral Health Research & Hunan 3D Printing Engineering Research Center of Oral Care & Hunan Clinical Research Center of Oral Major Diseases and Oral Health & Xiangya Stomatological Hospital and Xiangya School of Stomatology, Central South University, Changsha, China
J Cancer Res Ther ; 20(2): 706-711, 2024 Apr 01.
Article em En | MEDLINE | ID: mdl-38687943
ABSTRACT

BACKGROUND:

Oral submucous fibrosis (OSF) is a precancerous lesion, with oral squamous cell carcinoma (OSCC) being the most prevalent malignancy affecting the oral mucosa. The malignant transformation of OSF into OSCC is estimated to occur in 7-13% of cases. Myofibroblasts (MFs) play pivotal roles in both physiological and pathological processes, such as wound healing and tumorigenesis, respectively. This study aimed to explore the involvement of MFs in the progression of OSF and its malignant transformation. MATERIALS AND

METHODS:

In total, 94 formalin-fixed paraffin-embedded tissue blocks were collected, including normal oral mucosa (NOM; n = 10), early-moderate OSF (EMOSF; n = 29), advanced OSF (AOSF; n = 29), paracancerous OSF (POSF; n = 21), and OSCC (n = 5) samples. Alpha-smooth muscle actin was used for the immunohistochemical identification of MFs.

RESULTS:

NOM exhibited infrequent expression of MFs. A higher staining index of MFs was found in AOSF, followed by EMOSF and NOM. Additionally, a significant increase in the staining index of MFs was found from EMOSF to POSF and OSCC. The staining index of MFs in NOM, EMOSF, AOSF, POSF, and OSCC was 0.14 ± 0.2, 1.69 ± 1.4, 2.47 ± 1.2, 3.57 ± 2.6, and 8.86 ± 1.4, respectively. All results were statistically significant (P < 0.05).

CONCLUSIONS:

The expression of MFs exhibited a gradual increase as the disease progressed from mild to malignant transformation, indicating the contributory role of MFs in the fibrogenesis and potential tumorigenesis associated with OSF.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Oral Submucosa / Neoplasias Bucais / Imuno-Histoquímica / Transformação Celular Neoplásica / Miofibroblastos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fibrose Oral Submucosa / Neoplasias Bucais / Imuno-Histoquímica / Transformação Celular Neoplásica / Miofibroblastos Idioma: En Ano de publicação: 2024 Tipo de documento: Article