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口腔潜在恶性病变中的染色体异常和非整倍体:舌的独特特征。

Chromosomal aberrations and aneuploidy in oral potentially malignant lesions: distinctive features for tongue.

机构信息

Department of Diagnostic Oncology, Translational Oncopathology, National Institute for Cancer Research, Genoa, Italy.

出版信息

BMC Cancer. 2011 Oct 13;11:445. doi: 10.1186/1471-2407-11-445.

Abstract

BACKGROUND

The mucosae of the oral cavity are different at the histological level but appear all equally exposed to common genotoxic agents. As a result of this exposure, changes in the mucosal epithelia may develop giving rise to Oral Potentially Malignant Lesions (OPMLs), which with time may in turn progress to Oral Squamous Cell Carcinomas (OSCCs). Therefore, much effort should be devoted to identify features able to predict the likeliness of progression associated with an OPML. Such features may be helpful in assisting the clinician to establish both appropriate therapies and follow-up schedules. Here, we report a pilot study that compared the occurrence of DNA aneuploidy and chromosomal copy number aberrations (CNAs) in the OPMLs from different oral anatomical subsites.

METHODS

Samples from histologically diagnosed OPMLs were processed for high resolution DNA flow cytometry (hr DNA-FCM) in order to determine the relative DNA content expressed by the DNA index (DI). Additionally, array-Comparative Genomic Hybridization (a-CGH) analysis was performed on DNA obtained from diploid nuclei suspensions directly. When aneuploid nuclei were detected, these were physically separated from diploid nuclei on the base of their DI values by means of a DNA-FCM-Sorter in order to improve the a-CGH analysis.

RESULTS

Tongue OPMLs were more frequently associated with DNA aneuploidy and CNAs than OPMLs arising from all the other mucosal subsites.

CONCLUSIONS

We suggest that the follow-up and the management of the patients with tongue OPMLs should receive a distinctive special attention. Clearly, this hypothesis should be validated in a prospective clinical study.

摘要

背景

口腔黏膜在组织学水平上有所不同,但都同样容易受到常见遗传毒性物质的影响。由于这种暴露,黏膜上皮可能会发生变化,从而导致口腔潜在恶性病变(OPML),随着时间的推移,这些病变可能会进一步发展为口腔鳞状细胞癌(OSCC)。因此,应该努力识别能够预测与 OPML 相关进展可能性的特征。这些特征可能有助于临床医生确定适当的治疗方案和随访计划。在这里,我们报告了一项比较不同口腔解剖部位 OPML 中 DNA 非整倍体和染色体拷贝数异常(CNAs)发生情况的初步研究。

方法

对组织学诊断为 OPML 的样本进行高分辨率 DNA 流式细胞术(hr DNA-FCM)处理,以确定 DNA 指数(DI)所表示的相对 DNA 含量。此外,还直接从二倍体核悬浮液中对 DNA 进行了阵列比较基因组杂交(a-CGH)分析。当检测到非整倍体核时,根据其 DI 值,通过 DNA-FCM 分选器将其与二倍体核物理分离,以改善 a-CGH 分析。

结果

与其他所有黏膜部位的 OPML 相比,舌 OPML 更常与 DNA 非整倍体和 CNAs 相关。

结论

我们建议对舌 OPML 患者的随访和管理应给予特别关注。显然,这一假设应该在前瞻性临床研究中得到验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa4/3229618/005e4eba5123/1471-2407-11-445-1.jpg

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