Department of Pathology, The First Clinical College of Harbin Medical University, Harbin, The People's Republic of China.
J Clin Pathol. 2012 Oct;65(10):888-95. doi: 10.1136/jclinpath-2012-200909. Epub 2012 Jul 26.
Interface zone fibroblasts (INFs) are very important in the progression and metastasis of tumours but their effect on the invasion and migration of gastric cancer cells is still unclear.
Primary fibroblasts were isolated from the distal normal zone (normal zone fibroblasts, NFs), interface zone (INFs) and tumour zone (cancer-associated fibroblasts, CAFs) of 60 human gastric carcinoma tissue samples. The crosstalk between these fibroblasts and human gastric cancer MGC-803 cells was evaluated using an indirect co-culture model in vitro.
A high level of fibroblast activation protein (FAP) in the invasion front of gastric cancer was found in the gastric cancer tissue samples and no FAP expression was found in 20 normal gastric tissue samples by immunohistochemistry. High FAP expression was associated with Lauren classification, degree of differentiation, tumour node metastasis stage and depth of tumour invasion (p<0.05 or p<0.01). INFs promoted invasion and migration of MGC-803 cells. The number of invasions in INFs, CAFs and NFs were 120.10±27.53 (95% CI 102.12 to 138.10), 63.00±14.80 (95% CI 53.33 to 72.67) and 14.22±6.20 (95% CI 10.17 to 18.27), respectively; the number of invasions in INFs were 8.45-fold and 1.89-fold higher than those in NFs and CAFs, respectively (p<0.05). The number of migrations in INFs, CAFs and NFs were 118.00±16.83 (95% CI 107.00 to 129.00), 61.00±16.36 (95% CI 50.31 to 71.69) and 24.00±11.52 (95% CI 16.47 to 31.53), respectively; the number of migration in INFs were 4.91-fold and 1.92-fold higher than those in NFs and CAFs, respectively (p<0.05). INFs also significantly promoted cell proliferation and inhibited apoptosis in MGC-803 cells compared with NFs and CAFs (p<0.05).
These findings indicate that INFs exhibit a more robust biological modulatory activity than CAFs and NFs. INFs may be a key factor leading to tumour progression and metastasis and may be of use as a tool for post-treatment surveillance.
界面区成纤维细胞(INFs)在肿瘤的进展和转移中非常重要,但它们对胃癌细胞侵袭和迁移的影响尚不清楚。
从 60 个人胃癌组织样本的远端正常区(正常区成纤维细胞,NFs)、界面区(INFs)和肿瘤区(癌相关成纤维细胞,CAFs)中分离原代成纤维细胞。在体外通过间接共培养模型评估这些成纤维细胞与人类胃癌 MGC-803 细胞之间的串扰。
免疫组织化学显示,在胃癌组织样本中,胃癌侵袭前缘的成纤维细胞激活蛋白(FAP)水平较高,而在 20 个正常胃组织样本中未发现 FAP 表达。高 FAP 表达与 Lauren 分类、分化程度、肿瘤淋巴结转移分期和肿瘤浸润深度相关(p<0.05 或 p<0.01)。INFs 促进了 MGC-803 细胞的侵袭和迁移。在 INFs、CAFs 和 NFs 中的侵袭数量分别为 120.10±27.53(95%CI 102.12 至 138.10)、63.00±14.80(95%CI 53.33 至 72.67)和 14.22±6.20(95%CI 10.17 至 18.27);INFs 的侵袭数量分别是 NFs 和 CAFs 的 8.45 倍和 1.89 倍(p<0.05)。在 INFs、CAFs 和 NFs 中的迁移数量分别为 118.00±16.83(95%CI 107.00 至 129.00)、61.00±16.36(95%CI 50.31 至 71.69)和 24.00±11.52(95%CI 16.47 至 31.53);INFs 的迁移数量分别是 NFs 和 CAFs 的 4.91 倍和 1.92 倍(p<0.05)。与 NFs 和 CAFs 相比,INFs 还显著促进了 MGC-803 细胞的增殖并抑制了其凋亡(p<0.05)。
这些发现表明 INFs 比 CAFs 和 NFs 表现出更强的生物学调节活性。INFs 可能是导致肿瘤进展和转移的关键因素,并可能作为治疗后监测的工具。