Detection of head and neck squamous cell carcinoma among exfoliated oral mucosal cells by microsatellite analysis.

杂合子丢失 微卫星不稳定性 微卫星 唾液 头颈部鳞状细胞癌 病理 癌症 医学 表皮样癌 胃肠病学 头颈部癌 肿瘤科 内科学 生物 等位基因 遗传学 基因
作者
Michael Spafford,Wayne M. Koch,Andre L. Reed,Joseph A. Califano,Li Xu,Claus Ferdinand Eisenberger,Linwah Yip,Paul L. Leong,Wu Li,Shixi X. Liu,Carmen Jerónimo,William H. Westra,David Sidransky
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期刊:PubMed 卷期号:7 (3): 607-12 被引量:95
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Prompt detection of head and neck squamous cell carcinoma (HNSCC) is vital to successful patient management. In this feasibility study, we used microsatellite analysis to detect tumor-specific genetic alterations in exfoliated oral mucosal cell samples from patients with known cancer. Exfoliated mucosal cells in pretreatment oral rinse and swab samples were collected from 44 HNSCC patients and from 43 healthy control subjects (20 nonsmokers and 23 smokers). We tested a panel of 23 informative microsatellite markers to assay DNA from the matched lymphocyte, tumor (from cancer cases), and oral test samples. Loss of heterozygosity or microsatellite instability of at least one marker was detected in 38 (86%) of 44 primary tumors. Identical alterations were found in the saliva samples in 35 of these 38 cases (92% of those with markers; 79% overall) including 12 of 13 cases with small primaries [stage Tt or Tx (occult primary)] and 4 of 4 cases of patients that had undergone prior radiation. Microsatellite instability was detectable in the saliva in 24 (96%) of 25 cases in which it was present in the tumor, and loss of heterozygosity was identified in the test sample in 19 (61%) of 31 cases. No microsatellite alterations were detected in any of the samples from the healthy control subjects. This approach must now be refined and validated for the detection of clinically occult disease. Microsatellite analysis of oral samples may then become a valuable method for detecting and monitoring HNSCC.

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