Key Laboratory on Diagnosis and Treatment Technology on Thoracic Cancer, Zhejiang Cancer Hospital (Zhejiang Cancer Research Institute), Hangzhou, No. 38 Guangji Road, Banshanqiao District, Hangzhou, 310022, China.
Breast Cancer Res Treat. 2013 Jun;139(2):329-39. doi: 10.1007/s10549-013-2563-5. Epub 2013 May 14.
Cyclin D1 (CCND1), a key regulator of cell cycle progression, is overexpressed in many human cancers, including breast cancer. However, the impact of CCND1 overexpression in these cancers remains unclear and controversial. We conducted a systematic literature search in PubMed and EMBASE with the search terms "cyclin D1", "CCND1", "breast cancer", "prognosis", and potential studies for analysis were selected. Studies with survival data, including progression-free survival (PFS), overall survival (OS) or metastasis-free survival (MFS), were included in this meta-analysis. A total of 33 studies containing 8,537 cases were included. The combined hazard risk (HR) and its 95 % confidence interval (CI) of OS, PFS and MFS were 1.13 (95 % CI 0.87-1.47; P = 0.35), 1.25 (95 % CI 0.95-1.64; P = 0.12), and 1.04 (95 % CI 0.80-1.36; P = 0.76), respectively, for primary breast cancer patients with tumors exhibiting CCND1 overexpression. Interestingly, the impact of CCND1 expression on OS was a 1.67-fold (95 % CI 1.38-2.02; P = 0.00) increased risk for ER-positive breast cancer patients. However, CCND1 overexpression exhibited no association with the PFS or OS of patients who received epirubicin-based neoadjuvant chemotherapy, for which the P values were 0.63 and 0.47, respectively. In summary, CCND1 overexpression impacts the prognosis of ER-positive breast cancer patients, but not patients with unselected primary breast cancer or patients treated with neoadjuvant chemotherapy.
细胞周期蛋白 D1(CCND1)是细胞周期进程的关键调节因子,在许多人类癌症中过表达,包括乳腺癌。然而,CCND1 过表达在这些癌症中的影响仍不清楚且存在争议。我们在 PubMed 和 EMBASE 中进行了系统的文献检索,使用了“cyclin D1”、“CCND1”、“breast cancer”、“prognosis”等搜索词,并选择了潜在的研究进行分析。本荟萃分析纳入了包含生存数据的研究,包括无进展生存期(PFS)、总生存期(OS)或无转移生存期(MFS)。共纳入 33 项研究,包含 8537 例病例。OS、PFS 和 MFS 的合并风险比(HR)及其 95%置信区间(CI)分别为 1.13(95%CI 0.87-1.47;P=0.35)、1.25(95%CI 0.95-1.64;P=0.12)和 1.04(95%CI 0.80-1.36;P=0.76),这些研究均为肿瘤中 CCND1 过表达的原发性乳腺癌患者。有趣的是,CCND1 表达对 OS 的影响,对于 ER 阳性乳腺癌患者,风险增加了 1.67 倍(95%CI 1.38-2.02;P=0.00)。然而,CCND1 过表达与接受表阿霉素为基础的新辅助化疗的患者的 PFS 或 OS 无关,其 P 值分别为 0.63 和 0.47。总之,CCND1 过表达影响 ER 阳性乳腺癌患者的预后,但不影响未经选择的原发性乳腺癌患者或接受新辅助化疗的患者。