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维甲酸作为预防和治疗癌症的药物(第一部分)。

Retinoids as preventive and therapeutic anticancer agents (Part I).

作者信息

Lippman S M, Kessler J F, Meyskens F L

出版信息

Cancer Treat Rep. 1987 Apr;71(4):391-405.

PMID:3548957
Abstract

Retinoids, the synthetic and natural analogs of vitamin A, frequently block the phenotypic expression of cancer in vitro; they also inhibit growth and induce differentiation in many animal and human malignant cell types. Only recently has it become possible to propose a unifying mechanism of retinoid action, which involves the protein kinase-C cascade system. This system may mediate retinoids' many diverse actions, including their effects on enzyme synthesis, membrane properties, growth factors, binding proteins, genomic and postgenomic expression, the extracellular matrix, and immunologic responses. Ongoing in vitro studies of retinoid structure-activity relationships, effects on oncogene expression, reversal of drug-resistance, and, especially, the protein kinase-C cascade system should help clarify the precise mechanism of their anticancer action. Many in vitro and in vivo assay systems are available for testing the 2000 + synthetic retinoids. These assays indicate specific drug sensitivities, which may help focus future clinical trials. In human cancer prevention, retinoids have been most effective for skin diseases, including actinic keratosis, keratoacanthoma, and basal cell carcinoma; however, nondermatologic premalignancies, such as oral leukoplakia, bronchial metaplasia, laryngeal papillomatosis, cervical dysplasia, myelodysplastic syndromes, and the urinary bladder, also respond to retinoid therapy. Significant therapeutic advances are also occurring with this class of drugs in refractory malignancies, including advanced cutaneous squamous and basal cell cancer, mycosis fungoides, and acute promyelocytic leukemia. Newer third-generation retinoids, such as the highly potent retinoidal benzoic acid derivatives, are demonstrating therapeutic indexes far higher than earlier-generation retinoids. Current in vitro testing is also demonstrating that retinoids have synergistic activity in combination with other agents (eg, biologic modifiers, hormones, and DNA synthesis inhibitors) and treatment modalities (eg, irradiation). Notwithstanding the progress already made with retinoids in human cancer, many in vitro questions remain, and clinical work is just beginning.

摘要

类视黄醇是维生素A的合成类似物和天然类似物,常常在体外阻断癌症的表型表达;它们还能抑制多种动物和人类恶性细胞类型的生长并诱导其分化。直到最近,才有可能提出一种统一的类视黄醇作用机制,该机制涉及蛋白激酶C级联系统。这个系统可能介导类视黄醇的多种不同作用,包括它们对酶合成、膜特性、生长因子、结合蛋白、基因组和后基因组表达、细胞外基质以及免疫反应的影响。正在进行的关于类视黄醇结构-活性关系、对癌基因表达的影响、耐药性逆转,尤其是蛋白激酶C级联系统的体外研究,应有助于阐明其抗癌作用的确切机制。有许多体外和体内检测系统可用于测试2000多种合成类视黄醇。这些检测表明了特定的药物敏感性,这可能有助于确定未来的临床试验重点。在人类癌症预防中,类视黄醇对皮肤病最为有效,包括光化性角化病、角化棘皮瘤和基底细胞癌;然而,非皮肤的癌前病变,如口腔白斑、支气管化生、喉乳头状瘤病、宫颈发育异常、骨髓增生异常综合征和膀胱病变,也对类视黄醇治疗有反应。这类药物在难治性恶性肿瘤,包括晚期皮肤鳞状和基底细胞癌、蕈样肉芽肿和急性早幼粒细胞白血病方面也取得了重大治疗进展。更新的第三代类视黄醇,如高效的类视黄醇苯甲酸衍生物,其治疗指数远高于早期的类视黄醇。目前的体外检测还表明,类视黄醇与其他药物(如生物调节剂、激素和DNA合成抑制剂)以及治疗方式(如放疗)联合使用时具有协同活性。尽管类视黄醇在人类癌症治疗方面已经取得了进展,但仍有许多体外问题有待解决,临床工作才刚刚开始。

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