胃癌细胞与腹膜间皮相互作进用促腹膜纤维化致腹膜转移的研究  被引量:6

Interactions between Gastric Cancer Cells and Human Peritoneal Mesothelial Cells Causing Peritoneal Fibrosis and Carcinomatosis

在线阅读下载全文

作  者:那迪[1] 郭澎涛[1] 徐岩[1] 刘福囝[1] 王振宁[1] 邢承忠[1] 徐惠绵[1] 

机构地区:[1]中国医科大学附属第一医院肿瘤外科,沈阳市110001

出  处:《中国肿瘤临床》2012年第22期1716-1718,共3页Chinese Journal of Clinical Oncology

基  金:国家自然科学基金(编号:81071956)资助~~

摘  要:目的:研究间皮细胞对胃癌细胞的抵御作用,模拟游离癌细胞在接触腹膜前通过其分泌物导致的腹膜增厚、纤维化的过程,同时观察了间皮细胞对胃癌细胞迁移及侵袭能力的反作用。方法:用荧光显微镜观察共培养时间皮细胞对胃癌细胞的抵御作用;体内实验观察腹膜变化;电镜、光镜下观察体外实验中间皮层在胃癌-腹膜相互作用中的损伤和细胞骨架变化;采用Millicell小室共培养观察间皮细胞对胃癌细胞迁移及侵袭能力的反作用。结果:正常间皮细胞可防止肿瘤细胞对于腹膜的粘附,受损脱落后胃癌细胞可轻易粘附。体内外实验均显示接触胃癌细胞上清后腹膜间皮细胞受损、凋亡,并且受损残余的间皮可以反作用于癌细胞,使其迁移转移力提高。结论:正常间皮细胞可以抵御胃癌细胞的侵袭,受损伤刺激后的间皮细胞可以反作用于胃癌细胞促进其迁移及侵袭。Obje ctive: This study aims to describe the mechanism by which gastric cancer cells lead to an early peritoneal metas -tasis. Methods:Injured mesothelial cells were examined by fluorescence microscopy. A rat's parietal thickness was measured using he -matoxylin and eosin staining. Morphological changes in the human peritoneal mesothelial cells (HPMC) were observed under a scan-ning electron microscope and phase-contrast microscope. The cell migration capacity and the gastric cancer cell infestation were exam-ined using Millicell inserts in a chamber co-culture. Results: Mesothelial cells could prevent cancer cell infiltration into the sub-meso-thelial connective tissues. Conspicuous morphological changes were observed in the HPMC after the treatment with the gastric cancer cell supernatants. The supernatants induced the cytoskeleton reconstruction of HPMC. The injured mesothelial cells promoted invasion and metastasis in the gastric cancer cells. Conclusion:These findings indicate that gastric cancer cells can induce peritoneal fibrosis through supernatants during early peritoneal metastasis. However, the injured mesothelial cells can upregulate invasion and metastasis in gastric cancer cells.

关 键 词:胃癌 腹膜转移 腹膜纤维化 间皮细胞 

分 类 号:R735.2[医药卫生—肿瘤]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象