Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China; Shanghai Institute of Infectious Disease and Biosecurity, Fudan University, Shanghai, PR China.
Department of Pathology, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Cancer Genet. 2023 Nov;278-279:1-8. doi: 10.1016/j.cancergen.2023.07.004. Epub 2023 Jul 28.
Esophageal squamous cell carcinoma (ESCC) is the main subtype of esophageal cancer, with 5-year survival rate less than 30%. In order to offer an individual therapeutic approach, it is necessary to identify novel prognostic factors to recognize high-risk patients. Given the high frequency of CCND1 abnormalities and the important biological effects of smoking in ESCC, we explored the potential relationship between CCND1 abnormalities and smoking in ESCC patients. CCND1 status was examined by fluorescence in situ hybridization and immunohistochemical staining in ESCC tissue microarrays (n = 519). CCND1 amplification and cyclinD1 overexpression were found in 53.2 and 34.1% ESCC, respectively. CCND1 amplification (P = 0.142 for DFS and P = 0.191 for OS) and cyclinD1 overexpression (P = 0.035 for DFS and P = 0.092 for OS) tended to be poorer prognostic factors in all patients. Among smoking patients, those with CCND1 amplification had significantly poorer prognosis, with a median DFS and OS of 25.0 and 30.0 months compared to not reached and 52.0 months for those without CCND1 amplification (P = 0.020 and 0.018). A similar trend was found in the 68 patients with cyclinD1 overexpression (P = 0.043 and 0.048). Further univariate and multivariate analysis revealed CCND1 amplification was independently poorer prognostic factor in smoking patients, which was not found in non-smoking patients. Smokers with CCND1 amplification or cyclinD1 overexpression have poorer survival, which help us to identify distinct groups of patients with apparently poorer outcome and would enable appropriate follow-up and treatment strategies.
食管鳞状细胞癌(ESCC)是食管癌的主要亚型,5 年生存率低于 30%。为了提供个体化的治疗方法,有必要识别新的预后因素,以识别高危患者。鉴于 CCND1 异常的高频和吸烟在 ESCC 中的重要生物学效应,我们探讨了 CCND1 异常与 ESCC 患者吸烟之间的潜在关系。通过荧光原位杂交和免疫组织化学染色在 ESCC 组织微阵列(n=519)中检查 CCND1 状态。分别在 53.2%和 34.1%的 ESCC 中发现了 CCND1 扩增和 cyclinD1 过表达。在所有患者中,CCND1 扩增(DFS 的 P=0.142,OS 的 P=0.191)和 cyclinD1 过表达(DFS 的 P=0.035,OS 的 P=0.092)倾向于成为较差的预后因素。在吸烟患者中,具有 CCND1 扩增的患者预后明显较差,中位 DFS 和 OS 分别为 25.0 和 30.0 个月,而未达到的患者为 52.0 个月(P=0.020 和 0.018)。在 68 例 cyclinD1 过表达患者中也发现了类似的趋势(P=0.043 和 0.048)。进一步的单变量和多变量分析显示,CCND1 扩增是吸烟患者独立的较差预后因素,在非吸烟患者中则没有发现。具有 CCND1 扩增或 cyclinD1 过表达的吸烟者生存较差,这有助于我们识别出生存结局明显较差的不同患者群体,并能采取适当的随访和治疗策略。