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通过链特异性单克隆抗体监测不同类型人类肺癌中的细胞角蛋白。

Cytokeratins in different types of human lung cancer as monitored by chain-specific monoclonal antibodies.

作者信息

Broers J L, Ramaekers F C, Rot M K, Oostendorp T, Huysmans A, van Muijen G N, Wagenaar S S, Vooijs G P

机构信息

Department of Pathology, University Hospital Nijmegen, The Netherlands.

出版信息

Cancer Res. 1988 Jun 1;48(11):3221-9.

PMID:2452687
Abstract

The expression of cytokeratins (CKs) in human lung cancer was studied using chain-specific monoclonal antibodies to CKs 4, 7, 8, 10, 13, 18, and 19. When applied to adenocarcinomas (ACs) of the lung, high levels of CKs 7, 8, 18, and 19 were detected in all tumors, while CK 4 was found in high concentrations in some ACs. CK 10 and 13 were completely absent, or only present in low numbers of cells. Small cell lung cancers (SCLCs) and lung carcinoids contained CK 18 and sometimes 8 and 19, but no CK 7 in most cases. Three out of four tumors, histologically classified as SCLC, and expressing CK 7 in a variable number of cells were found by electron microscopic studies to contain regions with AC and/or squamous cell carcinoma (SQC) differentiation. The monoclonal antibody specific for CK 7 can therefore possibly help to distinguish AC differentiation within SCLC. CKs 10 and 13 were completely absent in SCLCs and lung carcinoids, while few CK 4-positive cells were found in some SCLCs and in one lung carcinoid. Within SQCs the monoclonal antibodies revealed a pronounced heterogeneity in CK expression. CKs 4, 7, 8, 10, 13, 18, and 19 could be detected, although not evenly distributed among all tumor cells. Highly differentiated SQCs expressed high levels of the CKs specific for squamoid differentiation, i.e., CKs 4, 10, and 13 in variable numbers of cells. With decreasing histologically detectable SQC differentiation these markers were gradually lost, while the number of cells containing CKs 7, 8, 18, and 19 increased. Application of this panel of monoclonal antibodies can therefore distinguish not only the main subtypes of lung cancer, but can also indicate the degree of differentiation and the degree of heterogeneity. These findings can be used as a diagnostic aid in lung tumor pathology, which may have an impact on treatment and prognosis.

摘要

利用针对细胞角蛋白(CK)4、7、8、10、13、18和19的链特异性单克隆抗体,研究了细胞角蛋白在人肺癌中的表达情况。将这些抗体应用于肺腺癌(AC)时,在所有肿瘤中均检测到高水平的CK7、8、18和19,而在一些AC中发现CK4浓度较高。CK10和13完全缺失,或仅存在于少量细胞中。小细胞肺癌(SCLC)和肺类癌含有CK18,有时还含有CK8和19,但在大多数情况下不含CK7。在组织学上分类为SCLC且在不同数量细胞中表达CK7的四分之三肿瘤中,通过电子显微镜研究发现含有腺癌和/或鳞状细胞癌(SQC)分化区域。因此,针对CK7的单克隆抗体可能有助于区分SCLC中的腺癌分化。在SCLC和肺类癌中,CK10和13完全缺失,而在一些SCLC和一例肺类癌中发现少量CK4阳性细胞。在SQC中,单克隆抗体显示CK表达存在明显异质性。虽然CK4、7、8、10、13、18和19并非在所有肿瘤细胞中均匀分布,但均可检测到。高分化SQC在不同数量细胞中表达高水平的鳞状分化特异性CK,即CK4、10和13。随着组织学上可检测到的SQC分化程度降低,这些标志物逐渐丢失,而含有CK7、8、18和19的细胞数量增加。因此,应用这组单克隆抗体不仅可以区分肺癌的主要亚型,还可以指示分化程度和异质性程度。这些发现可作为肺肿瘤病理学的诊断辅助手段,可能对治疗和预后产生影响。

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