背景:干细胞与自我更新和可塑性相关,并已在各种牙源性病变中与其发病机理和生物学行为相关的研究中进行了研究。我们的目的是对干细胞标志物在牙源性肿瘤和囊肿中的表达进行系统评价。
方法:通过MEDLINE/PubMed搜索文献,EMBASE通过OVID,WebofScience,通过EBSCO数据库和CINHAL,用于评估干细胞标志物在不同牙源性肿瘤/囊肿中表达的原始研究,或牙源性疾病组和对照组。这些研究的偏倚风险(RoB)是通过JoannaBriggs研究所批判性评估工具进行评估的。在至少两项研究中,对同一对牙源性肿瘤/囊肿中评估的标志物进行了荟萃分析。
结果:29项研究报道了干细胞标志物的表达,例如,SOX2,OCT4,NANOG,CD44,ALDH1,BMI1和CD105,在各种牙源性病变中,通过免疫组织化学/免疫荧光,聚合酶链反应,流式细胞术,微阵列,和RNA测序。Low,中度,在七个人中观察到高RoB,九,和十三项研究,分别。Meta分析显示,SOX2对成釉细胞癌或牙源性角化囊肿的辨别能力优于成釉细胞瘤。
结论:干细胞可能与牙源性病变的发病机制和临床行为有关,并且是未来个体化治疗的潜在靶标。
BACKGROUND: Stem cells have been associated with self-renewing and plasticity and have been investigated in various odontogenic lesions in association with their pathogenesis and biological behavior. We aim to provide a systematic
review of stem cell markers\' expression in odontogenic tumors and cysts.
METHODS: The literature was searched through the MEDLINE/PubMed, EMBASE via OVID, Web of Science, and CINHAL via EBSCO databases for original studies evaluating stem cell markers\' expression in different odontogenic tumors/cysts, or an odontogenic disease group and a control group. The studies\' risk of bias (RoB) was assessed via a Joanna Briggs Institute Critical Appraisal Tool. Meta-analysis was conducted for markers evaluated in the same pair of odontogenic tumors/cysts in at least two studies.
RESULTS: 29 studies reported the expression of stem cell markers, e.g., SOX2, OCT4, NANOG, CD44, ALDH1, BMI1, and CD105, in various odontogenic lesions, through immunohistochemistry/immunofluorescence, polymerase chain reaction, flow cytometry, microarrays, and RNA-sequencing. Low, moderate, and high RoBs were observed in seven, nine, and thirteen studies, respectively. Meta-analysis revealed a remarkable discriminative ability of SOX2 for ameloblastic carcinomas or odontogenic keratocysts over ameloblastomas.
CONCLUSIONS: Stem cells might be linked to the pathogenesis and clinical behavior of odontogenic pathologies and represent a potential target for future individualized therapies.