Neoplasma. 2016;63(3):462-70. doi: 10.4149/317_151013N525.
Nuclear factor-kappaB (NF-κB), especially p65 subunit, has been associated with origin and progression of cancer as well as with the resistance to radiotherapy and chemotherapy in experimental models. The aim of the present study was to determine expression of NF-κB/p65 in tumor specimens before and after treatment of rectal cancer patients and to evaluate possible relationship between expression of NF-κB/p65 before and after (chemo)radiotherapy, other tumor characteristics and the clinical outcome. Furthermore, NF-κB/p65 was studied in relationship to pathologic response to preoperative (chemo)radiotherapy. Fifty patients with rectal cancer undergoing neoadjuvant (chemo)radiotherapy and surgery were included in the study. Pre-treatment rectal cancer specimens were obtained from diagnostic colonoscopy. Post-treatment rectal cancer specimens were obtained from surgically removed part of the rectum with the tumor. NF-κB/p65 expression was determined by immunohistochemistry and analysis was performed both in biopsies and in post-treatment tumor samples. Cytoplasmic positivity in tumor cells and nuclear positivity in lymphocytes were detected. High NF-κB/p65 positivity in pre-treatment tumor samples was significantly associated with shortened overall survival (OS). Disease-free survival (DFS) tends to be shortened as well. In post-treatment tumor samples, high NF-κB/p65 positivity was neither associated with shortened OS nor with shortened DFS. In post-treatment samples residual tumor cells deeply infiltrating the wall of the rectum with high NF-κB/p65 expression were found. The cells were linked to significantly worse clinical outcome in terms of shortened OS and DFS. NF-κB/p65 positivity did not correlate with pathologic response to preoperative (chemo)radiotherapy. In conclusion, our data suggest that high level of NF-κB/p65 subunit may be associated with more aggressive features of the tumor, higher metastatic potential, and shortened overall survival, but it does not correlate with resistance to (chemo)radiotherapy. Consequently, the level of NF-κB/p65 may help to select those patients who have poor prognosis and are candidates for more intensive anticancer therapy. For these purposes both pre-treatment and post-treatment tumor samples may be used.
核因子-κB(NF-κB),尤其是 p65 亚基,与癌症的发生和发展以及实验模型中的放射治疗和化学疗法耐药性有关。本研究的目的是确定直肠癌患者治疗前后肿瘤标本中 NF-κB/p65 的表达,并评估 NF-κB/p65 治疗前后(放)化疗、其他肿瘤特征与临床结果之间的可能关系。此外,还研究了 NF-κB/p65 与术前(放)化疗病理反应的关系。本研究纳入了 50 例接受新辅助(放)化疗和手术的直肠癌患者。在诊断性结肠镜检查时获得治疗前直肠肿瘤标本。在手术切除直肠肿瘤的部分时获得治疗后直肠肿瘤标本。采用免疫组织化学法检测 NF-κB/p65 的表达,并对活检和治疗后肿瘤标本进行分析。检测肿瘤细胞的细胞质阳性和淋巴细胞的核阳性。治疗前肿瘤标本中 NF-κB/p65 阳性表达与总生存期(OS)缩短显著相关。无病生存期(DFS)也有缩短的趋势。在治疗后的肿瘤样本中,NF-κB/p65 高阳性表达与 OS 和 DFS 缩短均无相关性。在治疗后的样本中,发现高 NF-κB/p65 阳性表达的残留肿瘤细胞深度浸润直肠壁。这些细胞与 OS 和 DFS 缩短的临床结局显著相关。NF-κB/p65 阳性与术前(放)化疗的病理反应无相关性。总之,我们的数据表明,NF-κB/p65 亚基的高水平可能与肿瘤的侵袭性特征、更高的转移潜能和总生存期缩短有关,但与(放)化疗耐药性无关。因此,NF-κB/p65 的水平可能有助于选择预后不良且适合更强化抗癌治疗的患者。为此,可以使用治疗前和治疗后的肿瘤标本。