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乳腺癌中具有临床相关性的生物分子特征。

Biomolecular features of clinical relevance in breast cancer.

作者信息

Daidone Maria Grazia, Paradiso Angelo, Gion Massimo, Harbeck Nadia, Sweep Fred, Schmitt Manfred

机构信息

Research Unit # 10, Department of Experimental Oncology, Istituto Nazionale Tumori, Via Venezian 1, 20133 Milan, Italy.

出版信息

Eur J Nucl Med Mol Imaging. 2004 Jun;31 Suppl 1:S3-14. doi: 10.1007/s00259-004-1522-0. Epub 2004 Apr 17.

Abstract

Breast cancer is a heterogeneous disease and its consequent complexity is a major challenge for physicians and biologists. Notwithstanding its potential curability due to the availability of treatment modalities which are effective in the presence of favourable clinical or pathobiological features, there is still a great deal of controversy over its clinical management. In recent decades, tumour biomarkers that are indicative of or related to cell traits characterising malignancy--that is self-sufficiency in proliferative growth signals, insensitivity to growth inhibitory signals, evasion of apoptosis, limitless replicative potential, and activation of pathways leading to neo-angiogenesis, invasion and metastasis--have provided information that has been proven to be associated with disease progression. However, when these biomarkers have been analysed individually, their prognostic relevance has been found to be modest, the only remaining clinically useful biomarkers being cell proliferation and plasminogen activation-related factors for prognosis, and steroid hormone receptors and the oncogene HER2/neu for prediction of response to hormonal therapy or to the novel targeted anti-HER2/neu therapy. It therefore remains necessary to reduce the intrinsic complexity of breast cancer in order to improve its clinical outcome. One way to achieve this objective derives directly from the concept that cancer is a genetic disease at the somatic level and from the recent availability of high-throughput post-genomic analytical tools such as gene and protein expression techniques for global gene expression analysis. Following these novel approaches, a number of recent studies have produced gene expression profiles in breast cancer that are markedly associated with disease progression and directed to answer different clinical and biological questions. However, the outcome of these novel studies still needs to be validated, which will entail cooperation between different specialists and integration of all the different skills involved in translational research in oncology.

摘要

乳腺癌是一种异质性疾病,其复杂性给医生和生物学家带来了重大挑战。尽管由于存在有效的治疗方式,在具备有利的临床或病理生物学特征时乳腺癌具有潜在的可治愈性,但在其临床管理方面仍存在诸多争议。近几十年来,肿瘤生物标志物,即那些指示或与表征恶性肿瘤的细胞特征相关的标志物——也就是增殖生长信号的自给自足、对生长抑制信号不敏感、逃避凋亡、无限复制潜能以及导致新血管生成、侵袭和转移的信号通路激活——已提供了被证明与疾病进展相关的信息。然而,当单独分析这些生物标志物时,发现它们的预后相关性并不显著,目前临床上唯一仍有用的生物标志物是用于预后的细胞增殖和纤溶酶原激活相关因子,以及用于预测激素治疗或新型靶向抗HER2/neu治疗反应的类固醇激素受体和癌基因HER2/neu。因此,为了改善乳腺癌的临床结局,仍有必要降低其内在复杂性。实现这一目标的一种方法直接源于癌症是体细胞水平上的遗传疾病这一概念,以及近期出现的高通量后基因组分析工具,如用于全局基因表达分析的基因和蛋白质表达技术。遵循这些新方法,最近的一些研究得出了与乳腺癌疾病进展显著相关的基因表达谱,旨在回答不同的临床和生物学问题。然而,这些新研究的结果仍需验证,这需要不同专家之间的合作以及肿瘤转化研究中所有不同技能的整合。

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