Prusty Bhupesh K, Husain Syed Akhtar, Das Bhudev C
Division of Molecular Oncology, Institute of Cytology and Preventive Oncology (Indian Council of Medical Research), I-7, Sector-39, Gautam Budhh Nagar - 201301, NOIDA, India.
Front Biosci. 2005 May 1;10:1510-9. doi: 10.2741/1635.
Infection of specific types of 'high risk' HPVs such as HPV 16 and HPV 18 has been associated with the development of cervical cancer. Deregulation of specific NF-kappaB members has also been implicated with the development of many cancers including cervical cancer. We have studied the expression and DNA-binding activity of NF-kappaB during the development of cervical cancer involving cervical precancer, cancer and control tissues with or without HPV infection. We observed constitutive activation of NF-kappaB to a significant level in squamous-cell carcinomas while no or negligible NF-kappaB binding activity was observed in normal controls or precancerous lesions. Interestingly, there is a gradual increase in binding activity and expression of NF-kappaB from low-grade squamous intraepithelial lesions (LSIL) to high-grade squamous intraepithelial lesion (HSIL) and to invasive squamous cell carcinoma (SCC). On further dissection of NF-kappaB complex, the p50 subunit which generally heterodimerizes with p65 to form an active form NF-kappaB appears to form a p50/p50 homodimer instead of conventional p50/p65 heterodimer. In situ analysis of expression of p50 and p65 subunits by immunohistochemistry in tissue sections from different grades of cervical lesions including invasive cancer also demonstrate a gradual increase in the expression and nuclear localization of p50 subunit only as the severity of lesions increases. We have observed a very high expression of nuclear p50 in HSIL and invasive cancers while the level of nuclear p65 is significantly lower or nil. We further observed that this activation is not dependent on HPV infection since both HPV positive and HPV negative tumors showed the same pattern of high binding activity and increased expression of NF-kappaB p50/p50 homodimer. Although nuclear translocation and localization of p65 was observed to a lesser extent in invasive tumor, p65 was not found to be involved in dimmer formation. Thus the gradual activation and expression of NF-kappaB as a function of severity of cervical lesions and the change in dimerization pattern in favor of p50/p50 homodimers appears to play an important role during the development of cervical carcinoma.
特定类型的“高危”人乳头瘤病毒(HPV)感染,如HPV 16和HPV 18,与宫颈癌的发生有关。特定核因子κB(NF-κB)成员的失调也与包括宫颈癌在内的多种癌症的发生有关。我们研究了宫颈癌发生过程中NF-κB的表达及DNA结合活性,涉及有或无HPV感染的宫颈上皮内瘤变、癌症及对照组织。我们观察到,在鳞状细胞癌中NF-κB有显著的组成性激活,而在正常对照或癌前病变中未观察到或仅有可忽略不计的NF-κB结合活性。有趣的是,从低级别鳞状上皮内病变(LSIL)到高级别鳞状上皮内病变(HSIL)再到浸润性鳞状细胞癌(SCC),NF-κB的结合活性和表达逐渐增加。进一步分析NF-κB复合物发现,通常与p65异源二聚化形成活性形式NF-κB的p50亚基,似乎形成了p50/p50同源二聚体,而非传统的p50/p65异源二聚体。通过免疫组织化学对不同级别宫颈病变(包括浸润性癌)组织切片中p50和p65亚基表达的原位分析也表明,随着病变严重程度增加,仅p50亚基的表达和核定位逐渐增加。我们观察到HSIL和浸润性癌中核p50表达非常高,而核p65水平显著较低或为零。我们进一步观察到,这种激活不依赖于HPV感染,因为HPV阳性和HPV阴性肿瘤均表现出相同的高结合活性模式以及NF-κB p50/p50同源二聚体表达增加。尽管在浸润性肿瘤中观察到p65有程度较轻的核转位和定位,但未发现p65参与二聚体形成。因此,随着宫颈病变严重程度增加NF-κB的逐渐激活和表达以及二聚化模式向有利于p50/p50同源二聚体的方向改变,似乎在宫颈癌发生过程中起重要作用。