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口腔上皮异型增生的分子标志物:综述。

Molecular markers in oral epithelial dysplasia: review.

机构信息

Department of Oral Medicine and Pathology, Faculty of Dental Sciences, University of Peradeniya, Peradeniya, Sri Lanka.

出版信息

J Oral Pathol Med. 2009 Nov;38(10):737-52. doi: 10.1111/j.1600-0714.2009.00804.x.

Abstract

The clinical and histologic features alone cannot accurately predict whether potentially malignant disorders of the oral mucosa remain stable, regress or progress to malignancy. Some of them, with or without epithelial dysplasia, may transform to invasive oral squamous cell carcinomas (OSCC). Identification of molecular markers which can predict disease progression is necessary to improve the management of these disorders. Many genes and signaling pathways have been shown to be involved in the development of OSCC. This review summarizes some molecular markers researched in the detection of pre-cancer. We highlight selected markers that are reported to be significantly associated with progression of potentially malignant disorders to OSCC. These include alterations in genes/pathways which control cellular signaling, cell cycle, apoptosis, genomic stability, cytoskeleton, angiogenesis, etc. However, these genetic tumor markers have so far not gained any use in routine diagnosis and their utility in the prediction of risk of malignant transformation remains unknown. It is, however, clear from the large number of studies, some described in this review, that multiple genes/pathways are involved in the progression from normal to metaplastic/dysplastic, and subsequently to cancer. It is therefore necessary to study those significant alterations in multiple genes simultaneously in biopsy samples from large cohorts of subjects.

摘要

仅凭临床和组织学特征无法准确预测口腔黏膜的潜在恶性病变是否稳定、消退或进展为恶性肿瘤。其中一些病变,无论是否存在上皮异型增生,都可能转化为侵袭性口腔鳞状细胞癌(OSCC)。因此,有必要确定能够预测疾病进展的分子标志物,以改善这些病变的管理。许多基因和信号通路已被证明与 OSCC 的发生有关。本文综述了一些在癌前病变检测中研究的分子标志物。我们重点介绍了一些报道与潜在恶性病变进展为 OSCC 显著相关的选定标志物。这些标志物包括控制细胞信号转导、细胞周期、细胞凋亡、基因组稳定性、细胞骨架、血管生成等的基因/通路的改变。然而,到目前为止,这些遗传肿瘤标志物尚未在常规诊断中得到应用,其在预测恶性转化风险方面的效用尚不清楚。但是,从大量研究中可以清楚地看出,在从正常到化生/异型增生,再到癌症的进展过程中,涉及多个基因/通路。因此,有必要在大样本队列的活检样本中同时研究这些重要的多个基因的改变。

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