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用于临床癌症治疗的法尼基转移酶抑制剂的研发:聚焦血液系统恶性肿瘤

Development of farnesyltransferase inhibitors for clinical cancer therapy: focus on hematologic malignancies.

作者信息

Karp Judith E, Lancet Jeffrey E

机构信息

Division of Hematologic Malignancies, Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland 21231, USA.

出版信息

Cancer Invest. 2007 Sep;25(6):484-94. doi: 10.1080/07357900701359437.

Abstract

Farnesyltransferase inhibitors (FTIs) target and inhibit the peptide prenylating enzyme farnesyltransferase. This new class of signal transduction inhibitors is being tested clinically in diverse malignancies, with encouraging results in hematololgic malignancies and breast cancer in particuarl. Critical questions have yet to be answered, for example, optimal dose and schedule, disease subgroups most likely to respond, and appropriate combinations with standard cytotoxics and new biologics. Gene profiling studies of malignant target cells obtained during FTI clinical trials will help to identify patients who are likely to respond to FTIs and to develop mechanisms for overcoming FTI resistance. Clinical trials and correlative laboratory studies in progress and under development will define the optimal roles of FTIs in cancer patients.

摘要

法尼基转移酶抑制剂(FTIs)作用于并抑制肽类异戊二烯化酶法尼基转移酶。这类新型信号转导抑制剂正在多种恶性肿瘤中进行临床试验,尤其在血液系统恶性肿瘤和乳腺癌中取得了令人鼓舞的结果。一些关键问题尚未得到解答,例如最佳剂量和给药方案、最可能产生反应的疾病亚组,以及与标准细胞毒性药物和新型生物制剂的合适联合用药。在FTIs临床试验期间获取的恶性靶细胞基因谱研究将有助于识别可能对FTIs产生反应的患者,并开发克服FTI耐药性的机制。正在进行和正在开展的临床试验及相关实验室研究将明确FTIs在癌症患者中的最佳作用。

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