Tanigawa N, Morimoto H
Second Department of Surgery, Fukui Medical School.
Jpn J Cancer Res. 1990 Jun-Jul;81(6-7):687-91. doi: 10.1111/j.1349-7006.1990.tb02628.x.
One hundred and twenty-three specimens (83 primary and 40 metastatic) of colorectal cancers from 102 patients were subjected to the human tumor clonogenic assay (HTCA) to determine the clonogenicities of tumor specimens stratified by the degree of histological differentiation and of tumor progression. No statistically significant differences in the clonogenicity were observed among the tumors with different histological differentiation. Viable malignant cells were abundant in the primary tumor specimens with submucosal (sm) and muscular layer (pm) invasion, and decreased significantly in number per gram of wet specimen as the tumors progressed (P less than 0.05). Clonogenicity was also higher in "sm" and "pm" primary tumor specimens, and decreased as the tumors advanced (P less than 0.05). These findings suggest that, at the onset or in the relatively early phase of the tumor progression, tumors are medullary and have a large fraction of clonogenic cells, and that they then develop more stroma while losing the clonogenic cell fraction by tumor progression. HTCA appears to be still valuable for analysis of the changes in biological properties over time in large bowel tumors.
对来自102例患者的123份结直肠癌标本(83份原发肿瘤标本和40份转移肿瘤标本)进行了人肿瘤克隆形成试验(HTCA),以确定根据组织学分化程度和肿瘤进展分层的肿瘤标本的克隆形成能力。在不同组织学分化的肿瘤之间,未观察到克隆形成能力有统计学显著差异。在侵犯黏膜下层(sm)和肌层(pm)的原发肿瘤标本中,存活的恶性细胞数量丰富,并且随着肿瘤进展,每克湿标本中的细胞数量显著减少(P<0.05)。“sm”和“pm”原发肿瘤标本的克隆形成能力也较高,并且随着肿瘤进展而降低(P<0.05)。这些发现表明,在肿瘤进展的起始阶段或相对早期阶段,肿瘤为髓样,具有很大比例的克隆形成细胞,然后它们会形成更多的基质,同时随着肿瘤进展而失去克隆形成细胞比例。HTCA对于分析大肠肿瘤生物学特性随时间的变化似乎仍然具有价值。