Tang Ximing, Liu Diane, Shishodia Shishir, Ozburn Natalie, Behrens Carmen, Lee J Jack, Hong Waun Ki, Aggarwal Bharat B, Wistuba Ignacio I
Department of Thoracic/Head and Neck Medical Oncology, University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA.
Cancer. 2006 Dec 1;107(11):2637-46. doi: 10.1002/cncr.22315.
Nuclear factor-kappaB (NF-kappaB), a key transcription factor thought to play a major role in carcinogenesis, regulates many important signaling pathways involved in tumor promotion. Although NF-kappaB can be activated in lung cancer cell lines by tobacco exposure, there have been no studies of the expression of NF-kappaB in lung cancer pathogenesis.
The immunohistochemical expression of NF-kappaB p65 was investigated in 394 lung cancers (370 nonsmall cell lung carcinomas [NSCLC]; and 24 small cell lung carcinomas [SCLC]) and 269 lung normal epithelium and preneoplastic lesions, including hyperplasias, squamous metaplasias, dysplasias, and atypical adenomatous hyperplasias.
High levels of nuclear immunohistochemical expression of NF-kappaB p65 were detected in the lung cancers, with significantly higher levels in SCLCs compared with NSCLCs (P<.0001). In adenocarcinomas the NF-kappaB p65 expression level was significantly higher in advanced TNM stages (III-IV) than in earlier stages (I-II) (P<.0001), and when NF-kappaB p65 is dichotomized using 50% as the cutoff point (high vs low), a higher NF-kappaB p65 expression level was detected in tumors having either K-RAS (P = .02) or EGFR (P = .009) mutations compared with wildtype tumors. A relatively high level of nuclear NF-kappaB p65 expression was detected in normal and mildly abnormal epithelium, and a progression with increasing histology severity was detected in preneoplastic lesions.
NF-kappaB p65 nuclear expression is an early and frequent phenomenon in the pathogenesis of lung cancer. The findings indicate that NF-kappaB activation plays an important role in lung cancer pathogenesis and is a suitable target for the development of new lung cancer therapies and chemoprevention strategies.
核因子-κB(NF-κB)是一种关键的转录因子,被认为在致癌过程中起主要作用,它调控许多参与肿瘤进展的重要信号通路。尽管烟草暴露可在肺癌细胞系中激活NF-κB,但尚无关于NF-κB在肺癌发病机制中表达情况的研究。
对394例肺癌(370例非小细胞肺癌[NSCLC]和24例小细胞肺癌[SCLC])以及269例肺正常上皮和癌前病变(包括增生、鳞状化生、发育异常和非典型腺瘤样增生)进行NF-κB p65的免疫组化表达研究。
在肺癌中检测到高水平的NF-κB p65核免疫组化表达,SCLC中的表达水平显著高于NSCLC(P<0.0001)。在腺癌中,NF-κB p65表达水平在TNM晚期(III-IV期)显著高于早期(I-II期)(P<0.0001),当以50%为界值将NF-κB p65分为高表达和低表达时,与野生型肿瘤相比,K-RAS(P = 0.02)或EGFR(P = 0.009)突变的肿瘤中检测到更高的NF-κB p65表达水平。在正常和轻度异常上皮中检测到相对较高水平的核NF-κB p65表达,在癌前病变中发现随着组织学严重程度增加而呈现进展。
NF-κB p65核表达是肺癌发病机制中的一种早期且常见的现象。这些发现表明NF-κB激活在肺癌发病机制中起重要作用,是开发新的肺癌治疗和化学预防策略的合适靶点。