实用肝脏病杂志
實用肝髒病雜誌
실용간장병잡지
JOURNAL OF CLINICAL HEPATOLOGY
2014年
6期
632-635
,共4页
胡晓云%陈锦章%廖毓菁%黄静%郭亚兵
鬍曉雲%陳錦章%廖毓菁%黃靜%郭亞兵
호효운%진금장%료육정%황정%곽아병
原发性肝癌%富组氨酸糖蛋白%细胞增殖%体外
原髮性肝癌%富組氨痠糖蛋白%細胞增殖%體外
원발성간암%부조안산당단백%세포증식%체외
Hepatocellular carcinoma%Histidine-rich glycoprotein%Cell proliferation%In vitro
目的:检测原发性肝癌组织富组氨酸糖蛋白(HRG)的表达,及其在体外研究过表达富组氨酸糖蛋白质粒对肝癌细胞增殖能力的影响。方法采用免疫组化法检测8例肝癌组织HRG表达情况,采用Western blot法检测11例手术切除的肝癌组织和癌旁组织HRG表达的差异;在人肝癌细胞株MHCC-97H细胞中转染稳定过表达HRG质粒,使用流式细胞仪分析肝癌细胞的增殖能力。结果8例原发性肝癌组织HRG表达量较非肿瘤组织明显减少;另11例癌组织HRG表达量为(0.14±0.17),癌旁组织HRG相对表达量为(1.39±2.08),两者差异有统计学意义(P<0.05);稳定过表达HRG的人肝癌细胞株MHCC-97H细胞增殖比例为(1.72±1.19)%,显著低于对照组[(14.3±2.99)%,P<0.01]。结论原发性肝癌癌组织HRG表达明显减少,过表达HRG的肿瘤细胞增殖能力降低。
目的:檢測原髮性肝癌組織富組氨痠糖蛋白(HRG)的錶達,及其在體外研究過錶達富組氨痠糖蛋白質粒對肝癌細胞增殖能力的影響。方法採用免疫組化法檢測8例肝癌組織HRG錶達情況,採用Western blot法檢測11例手術切除的肝癌組織和癌徬組織HRG錶達的差異;在人肝癌細胞株MHCC-97H細胞中轉染穩定過錶達HRG質粒,使用流式細胞儀分析肝癌細胞的增殖能力。結果8例原髮性肝癌組織HRG錶達量較非腫瘤組織明顯減少;另11例癌組織HRG錶達量為(0.14±0.17),癌徬組織HRG相對錶達量為(1.39±2.08),兩者差異有統計學意義(P<0.05);穩定過錶達HRG的人肝癌細胞株MHCC-97H細胞增殖比例為(1.72±1.19)%,顯著低于對照組[(14.3±2.99)%,P<0.01]。結論原髮性肝癌癌組織HRG錶達明顯減少,過錶達HRG的腫瘤細胞增殖能力降低。
목적:검측원발성간암조직부조안산당단백(HRG)적표체,급기재체외연구과표체부조안산당단백질립대간암세포증식능력적영향。방법채용면역조화법검측8례간암조직HRG표체정황,채용Western blot법검측11례수술절제적간암조직화암방조직HRG표체적차이;재인간암세포주MHCC-97H세포중전염은정과표체HRG질립,사용류식세포의분석간암세포적증식능력。결과8례원발성간암조직HRG표체량교비종류조직명현감소;령11례암조직HRG표체량위(0.14±0.17),암방조직HRG상대표체량위(1.39±2.08),량자차이유통계학의의(P<0.05);은정과표체HRG적인간암세포주MHCC-97H세포증식비례위(1.72±1.19)%,현저저우대조조[(14.3±2.99)%,P<0.01]。결론원발성간암암조직HRG표체명현감소,과표체HRG적종류세포증식능력강저。
Objective To investigate the expression of histidine-rich glycoprotein (HRG) in hepatocellular carcinoma (HCC) and its impact on HCC cell proliferation. Methods Immunohistochemistry was used to detect the expression of HRG in 8 HCC specimens and Western blot to evaluate the expression of HRG in 11 surgical cancerous and its non-cancerous specimens. The cell proliferation was analyzed by flow cytometry after stable overexpression of HRG in MHCC-97H cells. Results Declined expression of HRG was found in all 8 cancerous tissues as compared to the non-tumor tissues;Similar results were obtained in 11 pairs of HCC and its para-carcinoma tissues;The relative expression of HRG/β-actin was(1.39±2.08) in para-carcinoma tissues,and (0.14 ± 0.17) in tumor tissue,with a significant difference between them (P<0.05);The cell proliferation of MHCC-97H cells overexpressing HRG was remarkably inhibited as compared with the mock cells [(1.72 ±1.19)% vs.(14.3 ± 2.99)%,P<0.01]. Conclusion HRG is down-regulated in HCC and HRG overexpression can inhibit HCC cell proliferation in vitro.