Hewitt R E, Powe D G, Griffin N R, Turner D R
Department of Histopathology, University of Nottingham Medical School, Queen's Medical Centre, UK.
Int J Cancer. 1991 Jul 30;48(6):855-60. doi: 10.1002/ijc.2910480611.
In colorectal cancer an association has been found between lack of epithelial basement membrane (EMB) immunostaining in the tumour centre and more extensive malignant spread. Interestingly, ultrastructural investigations suggest that EBM loss at the tumour periphery may be part of an invasive mechanism. To further assess the significance of EBM deficiencies in different tumour areas, we carried out a detailed study of the basement membrane laminin immunostaining patterns in 130 cases of colorectal carcinoma. We find that discontinuous EBM staining in the tumour centre is associated with poor tumour differentiation (p less than 0.005), presence of lymph-node metastases (p less than 0.02), and more advanced Dukes stage (p less than 0.02). The latter association is strengthened by excluding cases in which numerous polymorphonuclear leukocytes (PMNs) are present adjacent to EBM breaks, suggesting that these inflammatory cells are a confounding factor. Discontinuous EBM staining is more frequently observed in tumour deep to muscularis propria than in submucosal tumour (p less than 0.02), indicating intra-tumoral variation. At the tumour periphery, extensive EBM discontinuity shows no association with lymph-node involvement, but is linked with deeper local invasion (p less than 0.05). While EBM staining patterns around central and peripheral tumour glands are related (p less than 0.001), staining around peripheral glands is almost invariably more discontinuous. However, EBM lack at the tumour periphery is not as absolute as previously suggested, since in 18% of tumours fewer than 25% of peripheral tumour glands show EBM breaks. This appears consistent with the hypothesis that invasive changes at the tumour periphery are temporary and reversible.
在结直肠癌中,已发现肿瘤中心缺乏上皮基底膜(EMB)免疫染色与更广泛的恶性扩散之间存在关联。有趣的是,超微结构研究表明肿瘤周边的EBM缺失可能是侵袭机制的一部分。为了进一步评估不同肿瘤区域EBM缺陷的意义,我们对130例结直肠癌病例的基底膜层粘连蛋白免疫染色模式进行了详细研究。我们发现肿瘤中心的EBM染色不连续与肿瘤低分化(p<0.005)、存在淋巴结转移(p<0.02)以及更晚期的杜克分期(p<0.02)相关。通过排除在EBM断裂处附近存在大量多形核白细胞(PMN)的病例,后一种关联得到加强,这表明这些炎症细胞是一个混杂因素。与黏膜下肿瘤相比,在固有肌层深层的肿瘤中更频繁地观察到EBM染色不连续(p<0.02),表明肿瘤内存在差异。在肿瘤周边,广泛的EBM不连续与淋巴结受累无关,但与更深的局部浸润相关(p<0.05)。虽然肿瘤中央和周边腺体周围的EBM染色模式相关(p<0.001),但周边腺体周围的染色几乎总是更不连续。然而,肿瘤周边的EBM缺失并不像之前所认为的那样绝对,因为在18%的肿瘤中,少于25%的周边肿瘤腺体显示EBM断裂。这似乎与肿瘤周边的侵袭性变化是暂时且可逆的这一假设一致。