山东医药
山東醫藥
산동의약
SHANDONG MEDICAL JOURNAL
2014年
31期
7-10
,共4页
张丽娜%赵桂秋%林红%王谦%牛膺筠
張麗娜%趙桂鞦%林紅%王謙%牛膺筠
장려나%조계추%림홍%왕겸%우응균
视网膜母细胞瘤%血管生成拟态%缺氧诱导因子1α%缺氧
視網膜母細胞瘤%血管生成擬態%缺氧誘導因子1α%缺氧
시망막모세포류%혈관생성의태%결양유도인자1α%결양
retinoblastoma%vasculogenic mimicry%hypoxia inducing factor-1α%hypoxia
目的:观察人视网膜母细胞瘤( RB)中血管生成拟态( VM)形成情况及来源,探讨相关调控因子的作用。方法收集人RB组织的石蜡切片,采用HE染色、过碘酸-Schiff(PAS)/CD34双重染色观察RB中VM形成情况,计算血管生成拟态密度(VMD);采用免疫组织化学方法检测ATP结合转运蛋白G超家族成员2(ABCG2)、造血干细胞抗原CD133(AC133)、CD34表达,检测缺氧诱导因子1α(HIF-1α)及其下游因子EphA2、基质金属蛋白酶(MMP)-2表达。采用Pearson相关性分析法分析VMD与上述指标的关系。结果 HE染色显示部分RB组织中除有内皮细胞衬覆的血管外,还可见肿瘤细胞围成的不规则管腔(内有红细胞);PAS/CD34双重染色显示43份RB组织中VM阳性23例(53.48%),VMD为(26.52±8.72)个/HP,VM阳性率与RB分化程度呈负相关(r=-0.532)、与临床分期无明显相关。 VM阳性RB组织中ABCG2阳性细胞数显著多于阴性组织中(P<0.01),VM阳性组织中部分肿瘤细胞AC133表达阳性、VM阴性组织中未见AC133表达,所有RB组织中仅血管内皮细胞CD34阳性表达。 HIF-1α、EphA2、MMP-2在VM阳性组织中的表达均显著高于阴性组织(P均<0.01),VMD与三者表达均呈正相关(P均<0.01,r分别为0.694、0.630、0.795)。结论低分化RB组织中存在VM,其管壁构成可能主要来源于ABCG2阳性的肿瘤干细胞,HIF-1α及其下游因子EphA2、MMP-2表达上调可能促进VM形成。
目的:觀察人視網膜母細胞瘤( RB)中血管生成擬態( VM)形成情況及來源,探討相關調控因子的作用。方法收集人RB組織的石蠟切片,採用HE染色、過碘痠-Schiff(PAS)/CD34雙重染色觀察RB中VM形成情況,計算血管生成擬態密度(VMD);採用免疫組織化學方法檢測ATP結閤轉運蛋白G超傢族成員2(ABCG2)、造血榦細胞抗原CD133(AC133)、CD34錶達,檢測缺氧誘導因子1α(HIF-1α)及其下遊因子EphA2、基質金屬蛋白酶(MMP)-2錶達。採用Pearson相關性分析法分析VMD與上述指標的關繫。結果 HE染色顯示部分RB組織中除有內皮細胞襯覆的血管外,還可見腫瘤細胞圍成的不規則管腔(內有紅細胞);PAS/CD34雙重染色顯示43份RB組織中VM暘性23例(53.48%),VMD為(26.52±8.72)箇/HP,VM暘性率與RB分化程度呈負相關(r=-0.532)、與臨床分期無明顯相關。 VM暘性RB組織中ABCG2暘性細胞數顯著多于陰性組織中(P<0.01),VM暘性組織中部分腫瘤細胞AC133錶達暘性、VM陰性組織中未見AC133錶達,所有RB組織中僅血管內皮細胞CD34暘性錶達。 HIF-1α、EphA2、MMP-2在VM暘性組織中的錶達均顯著高于陰性組織(P均<0.01),VMD與三者錶達均呈正相關(P均<0.01,r分彆為0.694、0.630、0.795)。結論低分化RB組織中存在VM,其管壁構成可能主要來源于ABCG2暘性的腫瘤榦細胞,HIF-1α及其下遊因子EphA2、MMP-2錶達上調可能促進VM形成。
목적:관찰인시망막모세포류( RB)중혈관생성의태( VM)형성정황급래원,탐토상관조공인자적작용。방법수집인RB조직적석사절편,채용HE염색、과전산-Schiff(PAS)/CD34쌍중염색관찰RB중VM형성정황,계산혈관생성의태밀도(VMD);채용면역조직화학방법검측ATP결합전운단백G초가족성원2(ABCG2)、조혈간세포항원CD133(AC133)、CD34표체,검측결양유도인자1α(HIF-1α)급기하유인자EphA2、기질금속단백매(MMP)-2표체。채용Pearson상관성분석법분석VMD여상술지표적관계。결과 HE염색현시부분RB조직중제유내피세포츤복적혈관외,환가견종류세포위성적불규칙관강(내유홍세포);PAS/CD34쌍중염색현시43빈RB조직중VM양성23례(53.48%),VMD위(26.52±8.72)개/HP,VM양성솔여RB분화정도정부상관(r=-0.532)、여림상분기무명현상관。 VM양성RB조직중ABCG2양성세포수현저다우음성조직중(P<0.01),VM양성조직중부분종류세포AC133표체양성、VM음성조직중미견AC133표체,소유RB조직중부혈관내피세포CD34양성표체。 HIF-1α、EphA2、MMP-2재VM양성조직중적표체균현저고우음성조직(P균<0.01),VMD여삼자표체균정정상관(P균<0.01,r분별위0.694、0.630、0.795)。결론저분화RB조직중존재VM,기관벽구성가능주요래원우ABCG2양성적종류간세포,HIF-1α급기하유인자EphA2、MMP-2표체상조가능촉진VM형성。
Objective To observe the formation and origin of vasculogenic mimicry ( VM) in human retinoblastoma ( RB) and to investigate the roles of relevant regulatory factors .Methods We collected the human RB tissues to observe the formation of VM in human RB by HE staining and periodic acid-Schiff staining ( PAS)/CD34 double staining , and cal-culatee the VM density (VMD).The expression of ATP-binding cassette sub-family G member 2 (ABCG2), hemopoietic stem cell marker CD133(AC133), CD34, hypoxia inducible factor-1α(HIF-1α) and its downstream factors (EphA2 and matrix metalloproteinase 2 (MMP-2)) was detected by immunohistochemical method .The relationships among VM and the above indicators were analyzed by Pearson correlation analysis .Results HE staining showed blood vessels lined by endo-thelial cells as well as irregular lumen formed by tumor cells ( with red blood cells in it ) in some RB tissues .PAS/CD34 double staining showed 23 cases of positive VM (53.48%) in 43 RB samples, VMD was (26.52 ±8.72)/HP;the VM positive rate was negatively correlated with RB differentiation degrees (r =-0.532), and no significant correlation with the clinical stages .ABCG2 positive cells in the VM positive RB tissues were significantly more than those in the VM nega-tive RB tissues (P<0.01), a part of tumor cells expressed AC133 in the VM positive tissues, but not in the VM negative tissues, and only CD34 positive expression was observed in the vascular endothelial cells of all RB tissues .The expression of HIF-1α, EphA2 and MMP-2 in the VM positive group was significantly higher than that in the negative group ( all P<0.01), and the VMD is positively correlated with the three factors (all P<0.01; r=0.694, 0.630 and 0.795, respec-tively) .Conclusion VM exists in the poorly differentiated RB tissues , and its tube wall may mainly derive from ABCG 2 positive cancer stem cells .The up-regulated expression of HIF-1α, EphA2 and MMP-2 may promote the VM formation .