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类视黄醇对鳞状细胞癌生长和分化的抑制作用。

Suppression of squamous cell carcinoma growth and differentiation by retinoids.

作者信息

Lotan R

机构信息

Department of Tumor Biology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

Cancer Res. 1994 Apr 1;54(7 Suppl):1987s-1990s.

PMID:8137325
Abstract

The epithelium of the oral cavity is mostly nonkeratinizing. However, it undergoes an abnormal squamous differentiation with keratinization during vitamin A deficiency or oral carcinogenesis. Vitamin A analogues (retinoids) were found to be effective in preventing oral premalignant lesions and second primary cancers in the upper aerodigestive tract. Further development of retinoids for prevention and therapy of squamous cell carcinoma (SCC) requires a better understanding of their mechanism action on the growth and differentiation of SCC cells. We used cultured head and neck SCC (HNSCC) cell lines as a model system. Treatment of HNSCC cells with beta-all-trans-retinoic acid resulted in inhibition of growth (proliferation and colony formation) and suppression of squamous differentiation to varying degrees in the different cell lines. Because some of the malignant HNSCC cells recapitulate the main characteristics of keratinocyte squamous differentiation and responsiveness to retinoids, they can serve as a model for investigating the mechanism underlying the effects of retinoids on cell growth and differentiation. It is thought that nuclear retinoic acid receptors (RARs) and retinoid X receptors (RXRs) mediate the above effects of retinoids by acting as DNA-binding transcription-modulating factors. We found that HNSCC cell lines express several nuclear RAR and that their level could be modulated by retinoids in some cell lines. An inverse relationship was found between RAR-beta expression and squamous differentiation. An analysis of RAR mRNA expression in head and neck cancer specimens revealed a decrease in RAR-beta in premalignant and malignant tissues relative to normal mucosa. The expression of this receptor increased in vivo after treatment with 13-cis-retinoic acid. These results implicate the loss of RAR-beta expression in the development of head and neck cancer and suggest that RAR-beta could serve as an intermediate marker in prevention trials.

摘要

口腔上皮大多为非角化型。然而,在维生素A缺乏或口腔癌发生过程中,它会经历异常的鳞状分化并伴有角化。维生素A类似物(维甲酸)被发现可有效预防口腔癌前病变以及上呼吸道消化道的第二原发性癌症。进一步研发用于预防和治疗鳞状细胞癌(SCC)的维甲酸需要更好地了解其对SCC细胞生长和分化的作用机制。我们使用培养的头颈部SCC(HNSCC)细胞系作为模型系统。用β-全反式维甲酸处理HNSCC细胞导致不同细胞系中生长(增殖和集落形成)受到抑制,鳞状分化受到不同程度的抑制。由于一些恶性HNSCC细胞概括了角质形成细胞鳞状分化和对维甲酸反应性的主要特征,它们可作为研究维甲酸对细胞生长和分化影响机制的模型。据认为,核维甲酸受体(RARs)和维甲酸X受体(RXRs)作为DNA结合转录调节因子介导维甲酸的上述作用。我们发现HNSCC细胞系表达几种核RAR,并且在一些细胞系中它们的水平可被维甲酸调节。发现RAR-β表达与鳞状分化呈负相关。对头颈部癌标本中RAR mRNA表达的分析显示,与正常黏膜相比,癌前和恶性组织中RAR-β减少。用13-顺式维甲酸治疗后,该受体的表达在体内增加。这些结果表明RAR-β表达缺失与头颈部癌的发生有关,并提示RAR-β可作为预防试验中的一个中间标志物。

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