Evaluation of stromal myofibroblasts in oral submucous fibrosis and its malignant transformation: An immunohistochemical study

被引:1
作者
Liu, Ziyi [1 ,4 ,5 ]
Hu, Wenwu [1 ,4 ,5 ]
Shan, Zhongyan [1 ,5 ]
Liu, Sixuan [1 ,5 ]
Yao, Zhigang [2 ,3 ,5 ]
Quan, Hongzhi [1 ,5 ,6 ]
机构
[1] Cent South Univ, Dept Oral Maxillofacial Surg, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Stomatol Hosp, Dept Oral Pathol, Changsha, Peoples R China
[3] Cent South Univ, Sch Stomatol, Changsha, Peoples R China
[4] Yiyang Med Coll, Dept Oral Maxillofacial Surg, Yiyang, Peoples R China
[5] Cent South Univ, Xiangya Stomatol Hosp, Hunan Printing Engn Res Ctr Oral Care 3D, Hunan Clin Res Ctr Oral Major Dis & Oral Hlth, Changsha, Peoples R China
[6] CSU, Xiangya Stomatol Hosp & Stomatol Sch, 72 Xiangya Raod, Changsha 410008, Hunan, Peoples R China
关键词
Alpha smooth muscle actin; myofibroblasts; oral squamous cell carcinoma; oral submucous fibrosis; SQUAMOUS-CELL CARCINOMA; PATHOGENESIS; TGF-BETA-1; DISORDERS;
D O I
10.4103/jcrt.jcrt_498_23
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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收藏
页码:706 / 711
页数:6
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