| 王振芳,马泽坤,郑博源,祁光伟,阿仙姑·哈斯木.MICA/B蛋白在不同宫颈病变组织中的表达及意义[J].,2020,(12):2229-2233 |
| MICA/B蛋白在不同宫颈病变组织中的表达及意义 |
| Expression and Significance of Major Histocompatibility Complex Class I Related Protein A / B in Different Cervical Lesions |
| 投稿时间：2020-02-03 修订日期：2020-02-28 |
| DOI：10.13241/j.cnki.pmb.2020.12.006 |
| 中文关键词: 宫颈鳞状细胞癌 MICA蛋白 MICB蛋白 |
| 英文关键词: Cervical squamous cell carcinoma Major histocompatibility complex (MHC) class I chain-related protein A(MICA) Major histocompatibility complex (MHC) class I chain-related protein B(MICB) |
| 基金项目:新疆维吾尔自治区科技支疆项目（2018E02066）；国家自然科学基金项目（U1603119） |
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| 中文摘要: |
| 摘要 目的：探讨主要组织相容性复合物I类相关蛋白A/B（MICA/B）在不同宫颈病变组织及宫颈细胞系中的表达及定位。方法：采用免疫组织化学SP法检测宫颈炎症组织、高级别鳞状上皮内病变（high-grade squamous intraepithelial lesions, HSIL）及宫颈鳞癌（cervical squamous cell carcinoma, CSCC）组织中MICA/B蛋白的表达情况。采用免疫荧光化学与激光共聚焦显微术结合的方法研究3种宫颈癌细胞系C33a（HPV-）、Siha（HPV16+）、Hela（HPV18+）及正常宫颈上皮细胞系H8中MICA/B的表达和定位。结果：MICA/B蛋白主要表达定位于细胞浆，部分细胞核，在宫颈鳞癌组织中阳性表达率 (83.3%、81.8%)高于宫颈炎症组织(39.3%、44.0%)，差异具有统计学意义 (均有P<0.001)；MICA蛋白在HSIL组织的阳性表达率（81.8%）高于宫颈炎症组织（39.3%），差异具有统计学意义（P=0.002）；与分化程度、临床分期、淋巴结转移等临床病理参数之间比较无统计学差异（P>0.05）。结论：MICA蛋白随着宫颈组织病变的加重阳性表达率逐渐增高，MICB蛋白在宫颈癌组织的表达高于宫颈炎症组织。提示MICA/B蛋白可为宫颈癌的诊断及靶向治疗提供新方向。 |
| 英文摘要: |
| ABSTRACT Objective: To investigate the expression and localization of major histocompatibility complex (MHC) class I chain-related proteins A/B in cervical lesions tissues and cervical cancer cell lines. Methods: Immunochemistry SP method was used to detect the expression of MICA/B proteins in Cervicitis, SIL and CSCC tissues. The localization of MICA/B in three cervical cancer cell lines C33a(HPV-), Siha(HPV16+), Hela(HPV18+) and normal cervical epithelial cell line H8 were detected by using immunofluorescence and Laser confocal microscopy. Results: MICA/B proteins are mainly expressed in the cytoplasm and some nucleu,The positive expression rates in cancer tissues (83.3%, 81.7%) were significantly higher than those in cervicitis tissues(39.4%, 44.0%), The difference was statistically significant (P<0.000, P<0.001). The expression rate of MICA protein in HSIL tissues (81.8%) is higher than that in normal cervical tissues (39.3%), and the difference is statistically significant (P=0.002). There was no statistically significant difference with clinical pathological parameters such as the degree of differentiation, clinical stage, and lymph node metastasis (P>0.05). Conclusion: With the aggravation of cervical tissue lesions, the positive expression rate of MICA protein gradually increased, and the expression of MICB protein in cervical cancer tissues was higher than that in cervicitis tissues. It is suggested that MICA / B protein can provide a new direction for the diagnosis and targeted therapy of cervical cancer. |
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