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小细胞肺癌的分子发病机制。

The molecular pathogenesis of small cell lung cancer.

机构信息

Department of Medicine, Thoracic Oncology Service, Division of Solid Tumor Oncology, Memorial Sloan-Kettering Cancer Center and the Weill Medical College of Cornell University, New York, NY, USA.

出版信息

Cancer Biol Ther. 2010 Jul 1;10(1):1-10. doi: 10.4161/cbt.10.1.12045.

Abstract

Small cell lung cancer (SCLC) represents 13% of all lung cancer cases diagnosed in the United States. Although a chemotherapy and radiation-sensitive disease, SCLC recurs rapidly with only 5% of patients surviving five years. This dismal prognosis likely is secondary to few improvements in its treatment, without significant changes in its standard of care over the last three decades. SCLC has a unique biology with specific molecular and cellular changes, which are the subject of active investigation. Here, we summarize the alterations leading to the pathogenesis of SCLC: chromosomal changes; dysregulation of tumor suppressor genes, oncogenes, and signaling pathways; upregulation of receptor tyrosine kinases, growth factors and cellular markers; and the persistence of developmental pathways. Each of these represents potential targets for therapy and many biologic agents are being studied.

摘要

小细胞肺癌(SCLC)约占美国所有肺癌病例的 13%。尽管 SCLC 对化疗和放疗敏感,但仍迅速复发,仅有 5%的患者能存活五年。这种令人沮丧的预后很可能是由于其治疗方法几乎没有改善,过去三十年中其标准护理没有显著变化所致。SCLC 具有独特的生物学特性,存在特定的分子和细胞变化,这些变化是目前研究的热点。在这里,我们总结了导致 SCLC 发病机制的改变:染色体改变;肿瘤抑制基因、癌基因和信号通路的失调;受体酪氨酸激酶、生长因子和细胞标志物的上调;以及发育途径的持续存在。这些改变中的每一个都可能成为治疗的靶点,许多生物制剂正在被研究。

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