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经亚硝基甲基脲转化的致瘤性人乳头瘤病毒18型永生化人角质形成细胞中DCC肿瘤抑制基因的改变。

Alteration of the DCC tumor-suppressor gene in tumorigenic HPV-18 immortalized human keratinocytes transformed by nitrosomethylurea.

作者信息

Klingelhutz A J, Smith P P, Garrett L R, McDougall J K

机构信息

Division of Cancer Biology, Fred Hutchinson Cancer Research Center, Seattle, Washington 98104.

出版信息

Oncogene. 1993 Jan;8(1):95-9.

PMID:8380923
Abstract

A human papillomavirus type 18 (HPV-18)-immortalized human keratinocyte cell line (1811) has been transformed to tumorigenicity in nude mice by treatment with the carcinogen nitrosomethylurea (NMU). The NMU transformants (1811-NMU-T) showed additional chromosome alterations as compared with parental 1811 cells, including 18q deletion in two of two 1811-NMU-T lines analysed. Restriction fragment length polymorphism (RFLP) analysis indicated that both 1811-NMU-T lines had lost one allele of the 18q deleted in colon cancer (DCC) tumor-suppressor gene. Reverse transcriptase polymerase chain reaction (RT-PCR) showed that DCC expression was absent or barely detectable in the 1811-NMU-T cells as compared with 1811 or normal keratinocytes, suggesting that the remaining DCC allele in the 1811-NMU-T cells was also altered. These studies indicate that reduction or loss of DCC expression may be an important step in NMU transformation of HPV-immortalized cells to tumorigenicity.

摘要

人乳头瘤病毒18型(HPV - 18)永生化人角质形成细胞系(1811)经致癌物亚硝基甲基脲(NMU)处理后,在裸鼠体内已转化为具有致瘤性。与亲代1811细胞相比,NMU转化体(1811 - NMU - T)显示出额外的染色体改变,在所分析的两个1811 - NMU - T细胞系中,有两个出现了18号染色体长臂缺失。限制性片段长度多态性(RFLP)分析表明,两个1811 - NMU - T细胞系均丢失了结肠癌中缺失的18号染色体长臂(DCC)肿瘤抑制基因的一个等位基因。逆转录聚合酶链反应(RT - PCR)显示,与1811细胞或正常角质形成细胞相比,1811 - NMU - T细胞中DCC表达缺失或几乎检测不到,这表明1811 - NMU - T细胞中剩余的DCC等位基因也发生了改变。这些研究表明,DCC表达的减少或缺失可能是HPV永生化细胞经NMU转化为致瘤性的一个重要步骤。

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