Vangsted A J
Wallenberg Laboratory, University of Lund, Sweden.
APMIS. 1994 Aug;102(8):561-80. doi: 10.1111/j.1699-0463.1994.tb05206.x.
Serological tumor markers may become widely used as inexpensive and non-invasive methods of cancer detection. Markers of current interest for small cell lung cancer (SCLC) comprise enzymes, peptides, proteins, and carbohydrates. None of the serological markers for SCLC have yet proven to be of diagnostic value and at present their use is limited to monitoring disease and indicating prognosis. However, whilst serological markers related to the metabolic state of SCLC cells, such as neuron-specific enolase, serum thymidine kinase and tissue polypeptide antigen, may only be used for monitoring patients and for estimating prognosis, the other serological markers under current investigation may be used to indicate new treatment forms. Several novel approaches, including interference in the autocrine growth-regulating loop of SCLC by either peptides or antibodies, have been tried, SCLC is a highly heterogeneous tumor with respect to antigen expression, regulation of growth, and differentiation state. It is therefore important that new interventions are directed against both antigen-positive and antigen-negative tumor cells. For instance, radioisotopes or enzymes coupled to antibodies may be effective by exerting toxicity at some distance from the target. Antigens expressed on SCLC cells, such as peptide receptors involved in growth regulation, carbohydrate antigens like Lewis antigens, carcinoembryonic antigen and the ganglioside fucosylGM1, provide potential targets for antibody-conjugated therapy.
血清肿瘤标志物可能会作为廉价且无创的癌症检测方法而被广泛应用。目前对小细胞肺癌(SCLC)感兴趣的标志物包括酶、肽、蛋白质和碳水化合物。小细胞肺癌的血清学标志物尚未被证明具有诊断价值,目前其用途仅限于监测疾病和指示预后。然而,虽然与小细胞肺癌细胞代谢状态相关的血清学标志物,如神经元特异性烯醇化酶、血清胸苷激酶和组织多肽抗原,可能仅用于监测患者和评估预后,但目前正在研究的其他血清学标志物可用于指示新的治疗形式。已经尝试了几种新方法,包括通过肽或抗体干扰小细胞肺癌的自分泌生长调节环,小细胞肺癌在抗原表达、生长调节和分化状态方面是一种高度异质性的肿瘤。因此,重要的是新的干预措施要针对抗原阳性和抗原阴性肿瘤细胞。例如,与抗体偶联的放射性同位素或酶可能通过在距靶标一定距离处发挥毒性而有效。小细胞肺癌细胞上表达的抗原,如参与生长调节的肽受体、碳水化合物抗原如刘易斯抗原、癌胚抗原和神经节苷脂岩藻糖基GM1,为抗体偶联治疗提供了潜在靶点。