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小细胞肺癌的生物学异质性。

Biological heterogeneity of small cell lung cancer.

作者信息

Carney D N, Gazdar A F, Nau M, Minna J D

出版信息

Semin Oncol. 1985 Sep;12(3):289-303.

PMID:2996148
Abstract

Over the past 20 years considerable advances have been made in the characterization of the biologic properties of small cell lung cancer. The recognition that this histologic type of lung cancer, in contrast to the other major types of lung cancer, is highly sensitive to both chemotherapy and radiation therapy lead to significant improvements in the overall survival of patients with this disease. However, in spite of the initial major advances in therapy, overall results and survival have remained unchanged over the past 5 years. The majority of patients, although they will demonstrate an initial response to cytotoxic therapy, will ultimately die of their disease due to the development of drug resistance. Whether this development of drug resistance within a tumor cell represents the emergence of resistant clones of cells present at diagnosis, or a change within the cells exposed to cytotoxic therapy that renders them resistant to further therapy remains to be determined. The development of laboratory techniques that facilitate the culture and establishment of SCLC cell lines has greatly improved our understanding of the biology of SCLC, in addition to providing useful models for studies of mechanisms of drug resistance and metabolism. The ease of establishment of SCLC cell lines in defined medium suggests that these cells secrete "autocrine growth factors" essential for their growth in vitro. The characterization of these factors may provide an alternative means for treating this tumor in vivo. Moreover, by developing specific culture media for other types of lung cancer, similar advances in our knowledge of these tumors will occur. Although the growth of SCLC cells in a clonogenic assay may be of value in chemotherapy selection, the established cell lines provide a model for studying mechanisms of drug and radiation sensitivity; and drug metabolism. The recognition that SCLC cell lines have elevated levels of L-dopa decarboxylase has lead to the development of specific agents that may alter the growth of these cells through inhibition of polyamine synthesis. Such specifically designed therapy may become important in the future therapy of these patients. The establishment of cell lines has clearly indicated the considerable heterogeneity that exists in SCLC.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

在过去20年里,小细胞肺癌生物学特性的表征取得了显著进展。与其他主要类型的肺癌相比,这种组织学类型的肺癌对化疗和放疗都高度敏感,这一认识使该疾病患者的总体生存率有了显著提高。然而,尽管在治疗方面最初取得了重大进展,但在过去5年中总体结果和生存率并未改变。大多数患者虽然最初会对细胞毒性疗法产生反应,但最终会因耐药性的发展而死于该疾病。肿瘤细胞内这种耐药性的产生是代表诊断时就存在的耐药细胞克隆的出现,还是暴露于细胞毒性疗法的细胞发生变化从而使其对进一步治疗产生耐药性,仍有待确定。促进小细胞肺癌细胞系培养和建立的实验室技术的发展,极大地增进了我们对小细胞肺癌生物学的理解,同时也为耐药机制和代谢研究提供了有用的模型。在限定培养基中易于建立小细胞肺癌细胞系表明,这些细胞分泌对其体外生长至关重要 的“自分泌生长因子”。对这些因子的表征可能为体内治疗这种肿瘤提供另一种方法。此外,通过为其他类型的肺癌开发特定的培养基,我们对这些肿瘤的认识也将取得类似的进展。虽然在克隆形成试验中小细胞肺癌细胞的生长可能对化疗选择有价值,但已建立的细胞系为研究药物和放射敏感性机制以及药物代谢提供了一个模型。认识到小细胞肺癌细胞系中L-多巴脱羧酶水平升高,已促使开发出可能通过抑制多胺合成来改变这些细胞生长的特定药物。这种专门设计的疗法在这些患者的未来治疗中可能会变得很重要。细胞系的建立清楚地表明小细胞肺癌中存在相当大的异质性。(摘要截短至400字)

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