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[核因子-κB、Ki-67和基质金属蛋白酶-9在牙源性钙化囊肿中的表达]

[Expression of nuclear factor-kappaB, Ki-67 and matrix metalloproteinase-9 in calcifying odontogenic cyst].

作者信息

Gong Yan-ling, Wang Li, Chen Xin-ming, Wang Heng-kun, Wang Xin-hong

机构信息

Department of Stomatology, The Second Hospital of Weihai, Weihai Shandong 264200, China.

出版信息

Zhonghua Kou Qiang Yi Xue Za Zhi. 2006 Oct;41(10):627-30.

Abstract

OBJECTIVE

To evaluate the expression of nuclear factor-kappaB (NF-kappaB), Ki-67 and matrix metalloproteinase-9 (MMP-9) in calcifying odontogenic cyst (COC), in order to investigate the proliferation and invasion of COC.

METHODS

Twenty-six cases of COC were classified into calcifying cystic odontogenic tumor (CCOT), dentinogenic ghost cell tumor (DGCT) and ghost cell odontogenic carcinoma (GCOC) based on the WHO classification of odontogenic tumors in 2005. The specimens of COC and 10 classic ameloblastoma (AB) were examined immunohistochemically to determine the expression of NF-kappaB p65, Ki-67 and MMP-9.

RESULTS

NF-kappaB was mainly detected in the cytoplasm of most tumor cells, but was only detected in the nucleus of few tumor cells (rate of nuclear staining < 1%). The expression of Ki-67 was significantly higher in GCOC than in CCOT (P < 0.001), DGCT (P < 0.05) and AB (P < 0.005). MMP-9 was detected both in tumor cells and stromal cells. GCOC showed significantly higher percentage of MMP-9 positive cases in stromal cells than CCOT, DGCT and AB (P < 0.05).

CONCLUSIONS

NF-kappaB may minimally affect the progression and invasion of COC. GCOC shows significantly higher proliferative activity and aggressiveness than CCOT and DGCT. MMP-9 in stroma may play a key role in the invasion of GCOC.

摘要

目的

评估核因子-κB(NF-κB)、Ki-67和基质金属蛋白酶-9(MMP-9)在牙源性钙化囊肿(COC)中的表达,以研究COC的增殖和侵袭情况。

方法

根据2005年世界卫生组织牙源性肿瘤分类,将26例COC病例分为钙化囊性牙源性肿瘤(CCOT)、牙本质生成性影细胞瘤(DGCT)和影细胞牙源性癌(GCOC)。采用免疫组织化学方法检测COC标本及10例经典成釉细胞瘤(AB)中NF-κB p65、Ki-67和MMP-9的表达。

结果

NF-κB主要在大多数肿瘤细胞的细胞质中检测到,但仅在少数肿瘤细胞核中检测到(核染色率<1%)。GCOC中Ki-67的表达明显高于CCOT(P<0.001)、DGCT(P<0.05)和AB(P<0.005)。MMP-9在肿瘤细胞和基质细胞中均有检测到。GCOC基质细胞中MMP-9阳性病例的百分比明显高于CCOT、DGCT和AB(P<0.05)。

结论

NF-κB可能对COC的进展和侵袭影响极小。GCOC的增殖活性和侵袭性明显高于CCOT和DGCT。基质中的MMP-9可能在GCOC的侵袭中起关键作用。

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